US20060094715A1

US20060094715A1 - 5-Ht4 receptor antagonists for the treatment of heart failure

Info

Publication number: US20060094715A1
Application number: US10/514,386
Authority: US
Inventors: Finn Levy
Original assignee: Individual
Current assignee: Serodus AS; Medinnova AS
Priority date: 2002-05-16
Filing date: 2003-05-16
Publication date: 2006-05-04
Also published as: DK1503764T3; AU2003227949A1; EP1503764A1; ES2339234T3; US8829028B2; CA2485600A1; EP1503764B1; AU2009200050A1; GB0211230D0; HK1072012A1; AU2009200050B2; US20090169545A1; ATE454153T1; WO2003097065A1; AU2003227949B2; CA2485600C; DE60330857D1

Abstract

This invention provides the use of a 5-HT₄receptor antagonist in the manufacture of a medicament for treating or preventing heart failure. Particular heart disorders to be treated are selected from the group comprising chronic heart failure, congestive heart failure, chronic congestive heart failure and heart failure resulting from ischaemic heart disease. Methods of treating heart failure using 5-HT₄receptor antagonists and pharmaceutical compositions containing 5-HT₄receptor antagonists are also provided.

Description

The present invention relates to heart failure and in particular the use of 5-HT₄receptor antagonists for the treatment of heart failure and the symptoms associated therewith.
Heart failure is a disease that primarily affects the elderly and with a population which is ageing progressively it is likely that the prevalence of this disease will continue to increase. New and improved methods of treating heart failure are therefore required.
Heart disorders or diseases, which are generally characterised by impaired cardiac function, e.g. heart failure, affect a large number of people worldwide and in particular in the Western world. Heart disorders or diseases are responsible for a reduced quality of life and premature death in a significant proportion of sufferers. Heart disorders occur in men, women, and children of both sexes, but are particularly prevalent in men and in elderly or middle aged people.
Heart failure is characterized by impaired cardiac function either due to reduced pump function (systolic dysfunction) or reduced filling (diastolic dysfunction). There are a number of different causes of heart failure of which the most common in the western world is coronary artery disease. Other common causes are cardiomyopathy (primary or secondary), hypertension, valvular diseases, and congenital defects.
Approximately 70% of heart failure in the western world is caused by coronary artery disease, which is usually due to atherosclerosis. Atherosclerosis will result in narrowing of the vessels in the heart leading to inadequate blood supply to the myocardium (muscle cells). Such heart disorders which involve a reduced supply of blood to the heart are sometimes given the general term “ischemic heart disease”. Ischemic heart disease (or ischemic cardiomyopathy) is the major etiologic group of heart failure in the Western world.
A reduced blood supply to the heart can manifest itself as angina pectoris (pain in the chest), acute myocardial infarction (which is the result of acute coronary artery occlusion causing a damaged myocardium with scar tissue; such an area cannot sustain cardiac muscle function), and sudden deaths. If the blood supply to the heart is reduced over periods of weeks to years, or if the myocardium has been substantially weakened by infarction with scar tissue, the heart function will become weakened with reduced pumping ability leading to the clinical manifestation of chronic heart failure.
Congestive heart failure (CHF, of which chronic congestive heart failure (cCHF) is a subset), is characterised by impaired left ventricular function, increased peripheral and pulmonary vascular resistance and reduced exercise tolerance and dyspnea. Circulatory congestion results from the decrease in cardiac output or from the damming of blood in the veins behind the left or right heart.
The more common forms of heart failure that result from damage to the heart often cannot be cured, but treatment may improve symptoms.
Current treatment for heart failure is based partially on preventative measures such as controlling diet, for example reducing or excluding caffeine and sodium, weight loss and exercise. Surgical means are used in more serious cases, for example coronary bypass surgery which eases symptoms by increasing bloodflow to the heart, coronary angioplasty or transplantation, if the heart has lost significant pumping capacity.
Drug treatments are also used. For example angiotensin converting enzyme (ACE) inhibitors slow the progression of heart failure by inhibiting the formation of angiotensin and causing vasodilation. The use of other diuretics is also common, which relieve water retention in the body thus easing the workload on the heart. Digitalis preparations such as digoxin are also used to increase the force of the heart's contractions.
Betablockers are another commonly used treatment for heart failure, alone or in combination with ACE inhibitors. The failing heart is adrenergically activated, in contrast to the normally functioning human ventricle when in a resting state (Bristow, 2000, Circulation, Vol 101, 558-569). The increase in cardiac adrenergic drive appears to be damaging to the failing heart and is thus termed a maladaptive response. This response appears to be associated with changes in the composition of the adrenoceptors during heart failure with up-regulation of α₁adrenoceptors and the down-regulation of β adrenoceptors. In addition, mouse models overexpressing activated adrenoceptors show cardiomyopathy and systolic dysfunction. Chronic adrenergic signalling is therefore considered to be a harmful compensatory mechanism in the failing human heart.
In the end stage failing heart, 50-60% of the total signal transducing potential is lost. Blockade of the remaining signalling capacity using betablockers complements the heart's endogenous antiadrenergic strategy of desensitisation, which is considered to be an adaptive change (Bristow, 2000, Circulation, Vol 101, 558-569).
By inhibiting the remaining signalling potential of β adrenergic receptors using β blockers, a relatively effective method of treating heart failure has been developed and used with some success.
Nonetheless, whilst β blockers have been used with relative success, there is a continuing need for further drugs and treatments for heart disease. β blocker treatment is not successful for all patients as some patients show contraindications to β blockade such as reactive airways disease, sinus node or conduction system disease with bradycardia. Furthermore the target doses require careful manipulation and management for the desired result to be achieved. Another disadvantage is that some individuals do not respond to β-blockade (Bristow, 2000, Circulation, Vol 101, 558-569). The disadvantages of known treatments and increasing incidence of heart disease as the age of the population increases means that more treatments are required.
The present invention addresses this need and is based on the surprising discovery that 5-HT₄receptors mediate an inotropic response in rat papillary heart muscles from failing hearts, a response which is not observed in normal rat papillary heart muscles. Thus, an inotropic response to serotonin (5-HT) appears to be induced in the ventricles of failing hearts. This surprising observation suggests that this inotropic response may be a further maladaptive compensatory mechanism in the failing heart. Based on this, a new therapy is proposed, namely to reduce or prevent this inotropic response to 5-HT (5-hydroxytryptamine; serotonin) by blocking the 5-HT₄receptors e.g. by the use of 5-HT₄receptor antagonists. Thus, we propose that a potential new treatment for heart failure lies in the use of 5-HT₄receptor antagonists.
5-HT is known to affect the CNS, the heart and the gastrointestinal tract. Effects on the heart include positive inotropic, chronotropic and lusitropic effects, all of which have been detected to date only on human atrial tissue and not ventricular tissue. In the human atrium these effects are mediated via the 5-HT₄receptors. Activation of the 5-HT₄receptor, which is a 7 transmembrane G-protein coupled receptor causes the stimulation of adenylyl cyclase activity, activation of cAMP dependent protein kinase and the phosphorylation of proteins involved in excitation-contraction coupling.
The 5-HT₄class of receptors is one of 7 known classes of 5-HT receptors (5-HT_1-7). All but one of the identified receptors are 7 transmembrane-spanning G-protein coupled receptors. Several of these classes contain more than one member, encoded either by separate genes or by splice variants. The 5-HT₄receptor has at least eight splice variants (5-HT_4(a)-5-HT_4(h)). Preliminary studies have suggested that differential expression of these splice variants may occur in different tissues although it has also been shown that certain splice variants may be coexpressed in some tissues. The precise role of the different splice variants is not yet clear.
Previous studies have identified 5-HT responses in human and porcine atrial tissue, occurring via the 5-HT₄receptor, including increased heart rate, contractile force and hastening of relaxation. These studies failed to show any effect of 5-HT on human (Jahnel et al., 1992, Naunyn Schmiedeberg's Arch Pharmacol, Vol 346:482-485; Schoemaker et al European Journal of Pharmacology 1993 Vol 230, 103-105) and porcine (Schoemaker et al., 1992, Naunyn Schmiedeberg's Arch. Pharmacol, 346: 486-489; Lorrain et al. 1992, Eur J Pharmacol 229: 105-108; Saxena, 1992, Naunyn Schmiedeberg's Arch. Pharmacol, 346: 629-636) ventricles. In addition, 5-HT₄receptors were thought to be localised exclusively in the atrium (Blondel et al., 1998, Journal of Neurochemistry Vol 70(6), 2252-2261, Blondel et al., 1997, FEBS Letters Vol. 412, 465-474).
A recent publication by Bach et al (2001, Naunyn Schmiedeberg's Arch. Pharmacol, 363; 146-160) however shows that the mRNA encoding 5-HT₄receptors is detectable in all 4 chambers of the normal human heart by RT-PCR. Co-expression of the 5-HT_4(a)and 5-HT_4(b)variants in both cardiac atrium and ventricle was shown. However, no functional studies of the receptors were reported.
5-HT₄receptor antagonists (such as that disclosed by WO 93/02677) have been proposed for use in the treatment of atrial arrhythmias and stroke, in addition to irritable bowel syndrome, gastro-oesophageal reflux disease, anxiety and/or migraine (WO 91/16045, Kaumann 1994 TiPS Vol 15, 451-455).
No previous studies have suggested any involvement or effect of the 5-HT₄receptor on heart failure, or any effects of heart failure on this receptor.
As mentioned above, it has now surprisingly been shown that the potential inotropic response (the force of muscular contraction) to 5-HT differs in papillary muscles from non-failing and failing rat heart, and in particular that only papillary muscles from failing rat hearts show a response to 5-HT (see Example 1).
We have further surprisingly shown that this inotropic effect is mediated through 5-HT₄receptors. The observation that 5-HT₄receptors are functional in failing rat heart muscle, and not in normal rat heart muscle indicates that this induction and signalling may be a novel compensatory mechanism in heart failure. By the term “compensatory mechanism” it is meant that the heart adapts to its reduced ability to function, in an attempt to compensate for decreased pumping. The adaptation, as in this case, and in the case of the β-adrenergic system, may take the form of an adaptation, or induced changes in signalling mechanisms and pathways. Thus, blocking this compensatory mechanism, for example, by using an antagonist of 5-HT₄receptors, presents a novel and hitherto unforeseen treatment modality in combatting heart failure.
The fact that human papillary muscles taken from patients with different types of heart failure also exhibit an inotropic response to serotonin, that is mediated by 5-HT₄receptors (Example 6) confirms that this effect is not restricted to rats.
It has also been shown that 5-HT_4(b)mRNA levels are increased in left ventricle and in papillary muscle in rats with CHF.
Thus, in one aspect, the present invention provides the use of 5-HT₄receptor antagonists in the manufacture of a medicament for combatting heart failure.
Also provided is a method of combatting heart failure in a mammal, said method comprising administering a 5-HT₄receptor antagonist to said mammal. Particularly, an effective amount of said antagonist is administered.
In still a further aspect, the invention also provides a 5-HT₄receptor antagonist, or a pharmaceutical composition containing such an antagonist for use in combatting heart failure.
Still further, is provided the use of a 5-HT₄receptor antagonist for combatting heart failure.
The mechanism by which the inotropic response to 5-HT is induced in heart failure has not yet been elucidated, but in any event, it is not critical to the proposed new therapeutic approach. However, whilst not wishing to be bound by theory, the mechanism of induction of the inotropic response may result from a functional activation of pre-existing inactive receptors whether through a structural or topological change, or release of inhibition. Alternatively the pre-existing receptors may be transported to a location where they can act. The mechanism may alternatively be increased synthesis, or induction, of novel receptors through increased transcription or translation. It is therefore to be understood that “induction” may refer to any mechanism whereby the activity of the 5-HT₄receptor signalling pathway is increased when compared to the activity in a normal (e.g. non-failing) heart.
In particular, the “induction” includes any mechanism whereby the 5-HT₄receptor mediated inotropic response is induced or increased. An “increase” is preferably or conveniently a statistically significant increase, for example in a test for 5-HT₄receptor mediated response as described in Example 1, or in any other test for inotropic response known in the art or described in the literature.
The term “heart failure” as used herein includes any condition characterised by impaired cardiac function either due to reduced pump action (systolic dysfunction) or reduced filling (diastolic dysfunction). More particularly, heart failure implies impaired function of the myocardium of the heart. Particularly, chronic forms of heart failure (i.e. chronic heart failure) in general are concerned. Alternatively viewed, a subset of heart failure of particular interest is congestive heart failure (CHF), and especially chronic congestive heart failure (cCHF). However other forms of heart failure are encompassed by the invention. The invention does not however include other heart diseases or conditions which do not come under the general definition of heart failure, as above, such as atrial arrythmias which are excluded from the scope of this invention.
Thus, heart failure can be defined as a disorder which may result from any condition that reduces the ability of the heart to pump blood. Often the cause is decreased contractility of the myocardium resulting from diminished coronary blood flow (e.g. heart failure caused by coronary artery disease (CAD) or coronary ischemic disease), but failure to pump adequate quantities of blood can also be caused by damage to heart valves, external pressure around the heart, primary cardiac muscle diseases (e.g. idiopathic dilated cardiomyopathy) or any other abnormality which makes the heart a hypoeffective pump. As mentioned above, chronic heart failure is particularly concerned.
Thus included in the scope of the invention are ischaemic heart disease (ischaemic cardiomyopathy), particularly chronic ischaemic heart disease, chronic non-ischaemic cardiomyopathy including idiopathic dilated cardiomyopathy and cardiomyopathy due to hypertension.
Cardiac failure may be manifest in either of two ways: (1) by a decrease in cardiac output or (2) by a damming of blood in the veins behind the left or right heart. The heart can fail as a whole unit or either the left side or the right side can fail independently of the other. Either way this type of heart failure leads to circulatory congestion and, as a result is referred to as congestive heart failure (CHF).
Congestive heart failure can be divided into two phases, acute (short term and unstable) CHF and chronic (long term and relatively stable) CHF. The division between the two is difficult to define precisely, but generally acute CHF is the stage of failure which occurs immediately after heart damage (i.e. has a rapid onset and short course) and is associated with instability in cardiac function and circulation, for example a sudden drop in cardiac output. Providing the acute phase is not so severe as to result in death, the sympathetic reflexes of the body are immediately activated and can compensate for the sudden loss in cardiac function. Such compensation can often be so effective and rapid that it is possible that no noticeable effect on the patient will be felt if a patient remains calm.
After the first few minutes of an acute heart attack, a prolonged secondary state begins. This is characterized by a retention of fluid by the kidneys and by the progressive recovery of the heart over a period of several weeks to months up until the point at which the cardiac condition stabilises. This phase of stability is known as chronic CHF. Although the heart has compensated and stabilised it is still weak and may become progressively weaker.
This means therefore that although symptoms vary largely between patients, patients with chronic CHF characteristically have a reduced cardiac function. The most common manifestation of reduced cardiac performance is systolic dysfunction. For example such patients display a reduced left ventricular ejection fraction (LVEF) when compared to a “normal” person who has not suffered from heart failure. In normal persons left ventricular ejection fraction is usually above 60%, while an ejection fraction less than 40% is characterized as systolic dysfunction. Thus, a LVEF of less than 40% is characteristic of reduced heart function in patients with chronic CHF. Less common than systolic dysfunction is diastolic dysfunction in which the ejection fraction is relatively preserved (left ventricular EF>40%) or normal, but where left ventricular filling is reduced.
Other characteristics of reduced cardiac function such as for example a reduced right ventricular ejection fraction, reduced exercise capacity and impaired haemodynamic variables such as a decreased cardiac output, increased pulmonary arterial pressure and increased heart rate and low blood pressure are also often observed in patients with cCHF.
The New York Heart Association (NYHA) classification system divides heart disease into four classes, depending on the severity of disease. NYHA class I: Patient with cardiac disease but without resulting limitations of physical activity; Class II: Patient with cardiac disease resulting in slight limitation of physical activity. Class III: Patient with cardiac disease resulting in marked limitation of physical performance. They are comfortable at rest. Class IV: Patient with cardiac disease resulting in inability to carry on any physical activity without discomfort. Symptoms may be present at rest.
The invention may be used for the treatment of all classes of heart failure but particularly the classes II-IV.
As alluded to above, heart failure in general may be chronic or acute. Thus, while the acute phase of heart failure (for example CHF) is over relatively quickly, the stability associated with the chronic phase of heart failure (e.g. CHF) can take a matter of months to develop. Generally, a patient exhibiting symptoms of heart failure for greater than 3 months or more preferably greater than 6 months can be regarded as having chronic stable heart failure, providing that no further symptoms of acute (e.g. congestive) heart failure such as angina or evidence of myocardial infarction have occurred during this 3 month or 6 month period.
As was alluded to briefly above, the chronic heart failure to be treated according to the present invention may result from any cause, e.g. may be the result of a primary disease or may be secondary to another disease. In one preferred embodiment of the invention the chronic heart failure to be treated is secondary to either idiopathic dilated cardiomyopathy (IDCM) and/or coronary ischemic disease (coronary artery disease—CAD).
Particularly, in a further preferred embodiment, the heart failure to be treated according to the invention is post-infarction heart failure. It will be noted in this regard that the rat model used in Example 1, 2, 4 and 7 is a model of post-infarction heart failure caused by coronary artery ligation, which is a well characterised model of heart failure.
Other types of heart failure which may be treated according to the invention include heart failure induced by a constantly increased after load, such as hypertensive heart failure. A rat model for this is also available, wherein heart failure is induced by aortic banding. This model has also been used to show that the 5-HT₄receptor mediated effect is not specific to post infarction heart failure (see Example 5).
The term “combatting” as used herein includes both treatment and prevention.
The term “5-HT₄receptor antagonist” as used herein includes any agent, i.e. any compound, substance, molecule or composition (or any other agent) which may reduce or prevent any response, for example an inotropic response, to 5-HT in heart failure (i.e. the response (e.g. inotropic response) of the heart, or preferably of the myocardium). Thus the antagonist may be viewed as any agent capable of inhibiting the inotropic response to 5-HT, or any other physiological or biological response to 5-HT. This activity may readily be assessed using any appropriate response test, for example any inotropic response test, available in the art, for example as detailed in Example 1. Thus, an inhibition may be observed as a decrease (e.g. a statistically significant decrease) in the response in question (e.g. inotropic response) in the presence of the agent as compared with the response (e.g. inotropic response) in the absence of the agent (i.e. antagonist).
Any agent known in the art and/or reported in the literature as an antagonist of 5-HT₄receptors may be used (including inverse agonists and partial agonists etc. which may function as antagonists under particular conditions, e.g. dosages/concentrations etc.).
Thus, the term “5-HT₄receptor antagonist” as used herein includes any compound, molecule, substance, agent or composition which attenuates the effect of 5-HT on the 5-HT₄receptor. Such antagonism may be competitive or non-competitive. Competitive antagonists bind to the receptor at a region that overlaps with the agonist binding site, thereby preventing the binding of the agonist. The negative log of the molar concentration which at equilibrium would occupy 50% of receptors in the absence of ligand (pK_B) is the measure of potency of a competitive antagonist. Non-competitive antagonists bind to a site on the receptors other than the site of agonist binding and prevent agonist binding and/or receptor activation via an allosteric mechanism. In addition, antagonists may be reversible or irreversible. Antagonists may readily be identified by their activity at the 5-HT₄receptor using any suitable assay or test system, conveniently any in vitro system using cells expressing stably or transiently transfected recombinant 5-HT₄receptors or endogenous 5-HT₄receptors, such as those described by Bach et al., (2001, supra).
Classically, receptor antagonists are small organic compounds and these represent a preferred class of 5-HT₄receptor antagonists for use according to the present invention. However, other “compounds” or “agents” may also be used; so long as they meet the functional criterion of inhibiting an inotropic (or any other) response to 5-HT (e.g. by blocking or inhibiting a 5-HT₄receptor) their chemical or physical nature is unimportant. Thus, for example protein or peptide molecules may be used, which may be natural or synthetic, or derivatives or modifications of natural molecules. One such class of protein/peptide molecules is antibodies and their fragments or derivatives, including synthetic antibody-like molecules. Many such “binding molecules” based on antibodies are known in the art e.g. single chain antibodies, CDR grafted antibodies, chimeric antibodies etc., and all such molecules are included. Alternatively, peptides and other molecular products of display or other (e.g. combinatorial) libraries may be used; the literature describes the synthesis and selection of many such binding molecules or binding entities by such display or other methods, and these may be used, selected to bind to the 5-HT₄receptor.
Also included are the salts of such compounds, including both organic and inorganic salts (e.g. with alkali and alkaline earth metals, ammonium, ethanolamine, diethanolamine and meglumine, chloride, hydrogen carbonate, phosphate, sulphate and acetate counterions). Appropriate pharmaceutically and/or physiologically acceptable salts are well described in the pharmaceutical literature. In addition, some of these salts may form solvates with water or organic solvents such as ethanol. Such solvates are also included within the scope of this invention.
5-HT₄receptor antagonists may also be prepared as pro-drugs according to principles well known in the art (e.g. as compounds which release, or which convert to, the active antagonist form when administered to the patient).
5-HT₄receptor antagonists are known in the art and described in the literature (Clark, R. D. in 5-HT₄Receptors in the Brain and Periphery, ed R. Eglen 1998 Springer Verlag and R. G. Landes Company). Any such compounds may be used according to the present invention. Thus, for example 5-HT₄receptor antagonists may be selected from compounds comprising an aromatic ring structure with a hydrogen-bond acceptor as one substituent and a hydrogen-bond acceptor as a second substituent and a tertiary amine spaced with at least three bonds away from the aromatic ring.
The 5-HT₄receptor antagonists are preferably selected from compounds comprising an aromatic ring to which a carbonyl group is attached, and a basic nitrogen in the appended side chain. An oxygen atom is preferably adjacent to the carbonyl group.
Representative classes of suitable compounds include benzoate esters, benzoate amides, imidazolopyridines, aryl ketones, indoles, carbazimidamides, phenylcarbamates and phenylureas.
Further examples of 5-HT₄receptor antagonists that could be used in the invention include: SB203186, 1-piperidinyl-ethyl-1H-indole-3-carboxylate (Parker S G et. al. Naunyn Schmiedebergs Arch Pharmacol. 1995 December; 353(1): 28-35); GR113808, [1-[2-methylsulphonylamino ethyl]-4-piperidinyl]methyl1-methyl-1H-indole-3-carboxylate (Kaumann A J. Br J. Pharmacol. 1993 November; 110(3): 1172-4); SB207710, (1-butyl-4-piperidinyl)methyl 8-amino-7-iodo-1,4-benzodioxan-5-carboxylate (Kaumann A J et. al. Naunyn Schmiedebergs Arch Pharmacol. 1994 May; 349(5): 546-8); SDZ205557, 2-diethylaminoethyl-(2-methoxy-4-amino-5-chloro)benzoate (Lorrain J et. al. Eur J Pharmacol. 1992 Dec. 8; 229(1): 105-8); DAU 6285, endo-8-methyl-8-azabicyclo[3.2.1]oct-3-yl-2,3-dihydro-6-methoxy-2-oxo-1H-benzimidazole-1-carboxylate (Torres G E et. al. J Pharmacol Exp Ther. 1994 October; 271(1): 255-61); RS 39604, 1-[4-amino-5-chloro-2-(3,5-dimethoxybenzyloxy)phenyl]-3[1-[2-[(methylsulfonyl)amino]ethyl]-4-piperidinyl]-1-propanone hydrochloride (Leung E et. al. Naunyn Schmiedebergs Arch Pharmacol. 1996 July; 354(2): 145-56); SB 204070, (1-n-butyl-4-piperidinyl)methyl 8-amino-7-chloro-1,4-benzodioxane-5-carboxylate (Leung E. et al. supra); SB 207266, N-[(1-butyl-4-piperidinyl)methyl]-3,4dihydro-2H-[1,3]oxazino[3,2-a]indolelocarboxamide hydrochloride (Gaster L M et. al. J. Med Chem. 1995 Nov. 24; 38(24): 4760-3); SB205008, 1-butyl-1-methyl-4-piperidinylmethyl)-8-amino-7-chloro-1,4-ben zodioxan-5-carboxylate iodide (McLean P G and Coupar I M. Naunyn Schmiedebergs Arch Pharmacol. 1995 August; 352(2): 132-40); (1-Butyl-4-piperidinyl)methyl 8-amino-7-chloro-1,4-benzodioxane-5-carboxylate hydrochloride (Gaster L M et al. J Med Chem. 1993 Dec. 10; 36(25): 4121-3); N-3389, (endo-3,9-dimethyl-3,9-diazabicyclo[3,3,1]non-7-yl 1H-indazole-3-carboxamide dihydrochloride) (Hagihara K et. al. Eur J Pharmacol. 1994 Dec. 12; 271(1): 159-66); FK1052, [(+)-8,9-dihydro-10-methyl-7-[(5-methyl-4-imidazolyl)methyl]pyrido-[1,2-a]-indole-6(7H)-one hydrochloride] (Kadowaki M et. al. J Pharmacol Exp Ther 1993 July; 266(1): 74-80); ML10375,2-(cis-3,5-dimethylpiperidino)ethyl 4-amino-5-chloro-2-methoxybenzoate (Blondel O et. al. Br J Pharmacol. 1998 October; 125(4): 595-7); RS-23597-190, [3-(piperidine-1-yl)propyl-4-amino-5-chloro-2-methoxybenzoate hydrochloride] (Bonhaus D W et. al. J Pharmacol Exp Ther. 1994 October; 271(1): 484-93); GR125487, (1-[2-[(methyl-sulphonyl)amino] ethyl]-4-piperidinyl-methyl-5-fluoro-2-methoxy-1H-indole-3-carboxylate) (Gale et al 1994 Br. J. Pharmacol., 113, 120P); (3-α-tropanyl)-1H-indazole-3-carboxylic acid (WO91/16045); ICS205-930 (tropisetron) (Dumuis A. et al. (1998), Eur J. Pharmacology 146 187-188); R50595 (FR76530) (Meulemans A L and Schuurkes J A. (1992), Eur J. Pharmacol. 212(1):51-9); RS 100235 (Clark R. D. et al. (1995) Bioorg Med Chem Lett; 5; 2119-2122); RS100302 (Rahme et al., 1999, Circulation 100(9): 1942-4); LY353433, 1-(1-methylethyl)-N-[2-[4-[tricyclo[3.3.1.1 (3,7)]dec⁻¹-ylcarbonyl)amino]-1-piperidinyl]ethyl-1H-indazole-3-carboxamide, (Cohen M. L. et al. J Pharmacol Exp Ther 1996; 277(1): 97-104); RO116-0086, 2,3-dihydrobenzo[1,4]dioxine-5-carboxylic acid 1-butyl-piperidin-4-ylmethyl ester hydrochloride salt, (Joubert L. et al., J Biol Chem. 2002, 277: 2250); RO116-1148 (2,3-dihydrobenzo[1,4]-dioxine-5-carboxylic acid 1-butyl-piperidin-4-ylmethyl amide hydrochloride salt) Joubert et al. 2002, supra) A-85380 (WO94/08994); SB205800 (Drug Data Report (1993) 15 10:949); SB 207058 (Exp Opin Invest Drugs (1994) 3(7):767); SB 207226 (Marketletter 22-1 en 22-18 (1995)); SC-53606 (Yang D C et al (1993) J Pharmacol Exp Ther; 266(3):1339-47); SC 56184 (R&D Focus (1993) 2(37)10).
However other 5-HT₄receptor antagonists may also be used.
5-HT₄receptor antagonists are further described in the following patent documents: WO91/16045, WO93/02677, WO93/18036, WO93/05040, WO 93/03725, WO 93/05038, PCT/EP93/03054, PCT/GB93/01895, PCT/EP93/02808, PCT/GB93/02028, PCT/EP93/02775, PCT/EP93/02809, PCT/GB93/02130, PCT/GB94/00172 (all to Smith Kline Beecham plc), EP-A-501322 (Glaxo), U.S. Pat. No. 6,331,401 (Synaptic Pharmaceutical Corporation), US 20020128172 (GlaxoSmithKline), US 20030045452 (GlaxoSmithKline), US 20020019386 (GlaxoSmithKline), EP-A-322973 (GlaxoSmithKline), EP-A-18002 (Sandoz Limited), U.S. Pat. No. 5,872,134 (Smith Kline Beecham), EP-A-387431 (Beecham Group plc), EP-A-201165 (Beecham Group plc), EP-A-201165 (Beecham Group plc), EP-A-234872 (Adria), U.S. Pat. No. 4,859,683 (Rorer), EP-A-307172 (Lilly), U.S. Pat. No. 6,127,379 (Smith Kline Beecham), U.S. Pat. No. 6,002,009 (Boehringer Ingelheim), U.S. Pat. No. 5,929,089 (Synthelabo) and U.S. Pat. No. 5,726,187 (Smith Kline Beecham).
By definition, as explained above, the 5-HT₄receptor antagonists will inhibit any 5-HT₄receptor mediated action of 5-HT in the failing heart. The antagonist may thus for example inhibit all 5-HT₄receptor mediated actions. By inhibition is meant that the response to 5-HT, for example the inotropic response, when compared to an untreated individual, is reduced. This reduction includes any measurable decrease in a response to 5-HT (e.g. the ventricular inotropic response) in an individual when compared to the 5-HT response (e.g. the ventricular inotropic response) in an individual taken at an earlier time, before treatment. The measurable decrease will preferably be statistically significant. More preferably the measurable decrease will be such that the 5-HT response (e.g. the ventricular inotropic response) is substantially inhibited by the 5-HT₄receptor antagonist. Most preferably the response is blocked. By blocked it is meant that no measurable response (e.g. the inotropic response) to 5-HT is detected in the presence of the 5-HT receptor antagonist.
Especially preferably the decrease will be associated with the improved cardiac performance of the patient.
Cardiac performance may be assessed according to methods and practices well known in the art.
Given the nature of most forms of heart disease it is not to be expected that “treatment” in accordance with the present invention will result in a complete cure of the heart failure in question. Rather, “treatment” in accordance with the present invention includes an improvement or alleviation of any of the symptoms associated with the heart failure and also an improved quality of life for a patient and, ultimately a prolonged lifetime and improved survival. “Treatment” in accordance with the present invention also includes an improvement or increase of the functionality of the heart or, in other words an improvement or increase in cardiac function or performance. In particular, treatment in accordance with the present invention may result in an improvement or increase in any one or more of the symptoms and functional parameters associated with heart failure patients and in particular the following symptoms and parameters of the patient.
The first symptom and parameter associated with improved cardiac function in heart failure patients is an increase in ventricular ejection fraction and in particular left ventricular ejection fraction (LVEF). This can be assessed by standard methods well known and documented in the art, for example by echocardiography, ECG synchronized gated radionuclide ventriculography (MUGA scan), angiography or magnetic resonance (MR) imaging, and is normally carried out when the subject is at rest. An improvement in LVEF has been found to be associated with improved survival amongst CHF patients (Cintron et al., 1993, Circulation Vol 87, Supplement VI, 17-23). Thus, this is an important and advantageous parameter to be improved in subjects treated in accordance with the present invention. RVEF may also be increased.
Whilst an improvement of LVEF is particularly important for the overall improvement of heart function, a number of other parameters associated with cardiac performance may be improved in accordance with the present invention. One of these is a significant improvement in overall clinical status and thus clinical performance as evaluated by NYHA functional class. In other words the NYHA functional class of a patient may be reduced after treatment with 5-HT₄antagonists in accordance with the present invention. Such a clinical evaluation may normally be carried out by a trained cardiologist.
Also an improvement may be seen in exercise capacity of the patients, as measured by peak oxygen uptake and peak work load. As indicated above, a decreased exercise capacity is an inconvenient and potentially dehabilitating symptom of many heart failure patients. Methods for measuring exercise capacity are well known and documented in the art. For example exercise testing can be carried out using an electrically braked bicycle ergometer. An exemplary protocol might consist of a starting work rate of 20 W increasing by 20 W every second minute until exhaustion (defined as an inability to keep the pedalling rate steady at 60 rpm). Oxygen uptake (VO₂) can be measured using for example the EOS/SPRINT system. Peak VO₂, is taken as the highest VO₂observed.
Furthermore various improvements in hemodynamic status and echocardiographic variables may also be observed. These are again indicative of improved cardiac function. For example a significant decrease in pulmonary capillary wedged pressure and in pulmonary artery pressure may be observed, together with an increase in peak heart rate, peak systolic blood pressure and mitral velocity deceleration time. Echocardiographic variables may conveniently be measured by echocardiography carried out by a trained cardiologist and haemodynamic variables can conveniently be assessed by right-sided heart catheterization according to standard techniques.
Another important variable which may be assessed is the plasma level of Nt-proANP. An increased or generally high level of Nt-proANP has been recognised as a marker of cardiac dysfunction. Moreover, levels of Nt-proANP have been shown in the past to correlate with pulmonary artery pressures in CHF and provide important prognostic information in CHF patients (Gottlieb et al., J. Am. Coll. Cardiol. 1989; 13: 1534-1539). Levels of Nt-proANP in a blood sample can be measured in a number of ways well known and documented in the art, for example by radioimmunoassay. Prior to the immunoassay, plasma is separated from a blood sample taken from the patient again by methods well known and documented in the art.
The above described “improvement” or “increase” in the symptoms and parameters includes any measurable improvement or increase when the parameter in question is compared with the equivalent parameter in a non-treated individual or when the parameter in question is compared with the equivalent parameter in the same individual taken at an earlier time point (e.g. comparison with a “base line” level). Preferably the improvement or increase will be a statistically significant one. Especially preferably the improvement or increase in the symptoms and parameters will be associated with the improved health of the patient concerned and more preferably a prolonged survival.
Methods of determining the statistical significance of differences in parameters are well known and documented in the art. For example herein a parameter is generally regarded as significant if a statistical comparison using a two-tailed significance test such as a Student t-test or Mann-Whitney U Rank-Sum test shows a probability value of <0.05.
Thus, a further aspect of the present invention relates to the use of a 5-HT₄receptor antagonist in the manufacture of a medicament for use in the improvement of cardiac function, particularly cardiac function in heart failure.
In a yet further and more preferred aspect, the present invention relates to the use of a 5-HT₄receptor antagonist in the manufacture of a medicament for use in the increase of ventricular function, particularly preferably left ventricular function (e.g. LVEF), more particularly in heart failure.
A yet further aspect of the present invention relates to the use of a 5-HT₄receptor antagonist in the manufacture of a medicament for use in the reduction of plasma Nt-proANP levels. As mentioned above, a reduction in the plasma levels of Nt-proANP is an indicator of improved cardiac function and performance. “Reduction” as used herein includes any measurable reduction when the parameter in question is compared with the equivalent parameter in a non-treated individual or when the parameter in question is compared with the equivalent parameter in the same individual taken at an earlier time point (e.g. comparison with a “base line” level). Preferably the reduction is statistically significant as discussed above. Especially preferably the reduction in the levels of Nt-proANP will be associated with an improved feeling of health in the patient concerned and more preferably a prolonged survival.
Alternatively viewed, the invention provides a method of improving cardiac function in a mammal (for example a mammal with heart failure) which method comprises administering to said mammal a pharmaceutically effective amount of a 5-HT₄receptor antagonist.
The above described uses and methods are generally carried out on mammals. Any mammal may be treated, for example humans and any livestock or domestic animal, e.g. mice, rats, pigs, cats, dogs, sheep, rabbits, horses, cows or monkeys. However preferably the mammals are humans.
The 5-HT₄receptor antagonist is conveniently formulated in a pharmaceutical composition for use according to the present invention. Thus, as mentioned above in a further aspect, the present invention also provides a pharmaceutical composition for use in combatting heart failure, said composition comprising a 5-HT₄receptor antagonist together with at least one pharmaceutically acceptable carrier diluent or excipient.
The appropriate content of active ingredient in such compositions may be determined according to principles and procedures routine in the art and may readily be determined by the skilled practitioner. Thus, for example, the active ingredient in such compositions may comprise from 0.05% to 99% by weight of the formulation, for example from 0.1% to 1.0% or around 0.5%. The concentration of active ingredient in the formulation will depend on the type of formulation. For example, enteral products (e.g. tablets and capsules) can typically have 5% to 50% active ingredients by weight, whereas parenteral formulations usually have a lower concentration of active compound e.g. 0.1% to 3% active ingredient by weight, for example in an injection solution.
By “pharmaceutically acceptable” is meant that the ingredients must be compatible with other ingredients of the composition as well as physiologically acceptable to the recipient.
The pharmaceutical compositions may be formulated according to any of the conventional methods known in the art and widely described in the literature. Thus, the active ingredient (i.e. 5-HT₄receptor antagonist) may be incorporated, optionally together with other active substances, with one or more conventional carriers, diluents and/or excipients, to produce conventional galenic preparations which are suitable or can be made suitable for subcutaneous, intramuscular, intravenous or any other administration such as powders, sachets, cachets, elixirs, suspensions, emulsions, solutions, syrups, ointments, sterile injectable solutions, sterile packaged powders, and the like. The pharmaceutical composition comprising the 5-HT₄receptor antagonist may be prepared in a form appropriate for infusion or injection into a patient. Such infusion or injection is preferably intravenous (i.v.) but may also be given subcutaneously (s.c.) or intramuscularly (i.m.).
Preferably, the compositions may be provided in a form adapted for oral or parenteral administration. Alternative pharmaceutical forms thus include plain or coated tablets, capsules, suspensions and solutions containing the active component optionally together with one or more inert conventional carriers and/or diluents.
Examples of suitable carriers, excipients, and diluents are lactose, dextrose, sucrose, maltose, glucose, sorbitol, mannitol, starches, gum acacia, calcium phosphate, aglinates, tragacanth, gelatin, calcium silicate, microcrystalline cellulose, polyvinylpyrrolidone, cellulose, water syrup, water, water/ethanol, water/glycol, water/polyethylene, glycol, propylene glycol, methyl cellulose, methylhydroxybenzoates, propyl hydroxybenzoates, talc, magnesium stearate, mineral oil or fatty substances such as hard fat or suitable mixtures thereof. The compositions may additionally include lubricating agents, wetting agents, emulsifying agents, suspending agents, preserving agents, sweetening agents, flavouring agents, and the like. The compositions of the invention may be formulated so as to provide quick, sustained or delayed release of the active ingredient after administration to the patient by employing procedures well known in the art.
Solubilizing and/or stabilizing agents may also be used, e.g. cyclodextrins (CD) α, β, γ and HP-β cyclodextrin.
Suitable doses will vary from patient to patient and can be determined by the physician in accordance with the weight, age and sex of the patient, mode of administration, and the severity of the condition and also the particular antagonist used for treatment. Exemplary unit doses for oral administration contain 1 to 250 mg (and for parenteral administration contains preferably from 0.1 to 50 mg), of the active ingredient. The daily dose for oral administration is normally in the range of approximately 0.01 to 10 mg/kg/day, more usually 0.1 to 5 mg/kg/day, for example 0.1 to 2 mg/kg/day. For example a 70 kg adult would receive a daily dose of 1 to 700 mg or 0.7 to 700 mg, more usually 1 to 350 mg or 7 to 350 mg for example 7 to 140 mg. For intravenous or intramuscular administration the doses can be between 0.1 mg and 100 mg, preferably between 0.1 mg and 25 mg, the compound being administered 1 to 4 times a day.
The improvements seen in patients treated in accordance with the present invention may be immediate (e.g. after a few days), or may be seen after a few weeks or a few months depending on the individual patient. Once the initial improvement is seen, continued improvement over the subsequent weeks and months may also occur. As indicated above, treatment can be continued for as long as is desired or is necessary.
Use of a 5-HT₄receptor antagonist in accordance with the present invention may be in place of, or preferably in addition to (i.e. in combination with) the use of other drugs for treatment of heart failure. Thus, other drugs known to treat heart failure might be included in the pharmaceutical compositions described above or may be administered separately, in a manner appropriate for the drug concerned.
Thus, in a further aspect the present invention provides a product comprising (a) a 5-HT₄receptor antagonist and (b) a second drug (e.g. a second agent effective for the treatment of heart failure) as a combined preparation for simultaneous, separate or sequential use in the treatment of heart failure or in improving cardiac function.
Suitable 5-HT₄receptor antagonists are defined above. Suitable second drugs or agents are well known and documented in the art and include known drugs for use in the treatment of heart disorders, for example diuretics, vasodilators, inotropic drugs such as digoxin, or other compounds such as anticoagulants, β blockers, angiotensin II blockers, angiotensin converting enzyme inhibitors or aldosterone antagonists may be used as discussed above.
A particularly advantageous combination of 5-HT₄receptor antagonist is with β-blockers.
The invention will be further described with reference to the following non-limiting Examples with reference to the following drawings in which:
FIG. 1 shows the inotropic effect of serotonin in heart failure rats. Original paper recording in a papillary muscle from a representative Chronic heart failure rat. Serotonin (10 μmol/l) induced a positive inotropic response in the presence of atropine, timolol and prazosin. Inset: Development of the inotropic response, expressed as F_maxin percent of individual maximal response, in Chronic heart failure papillary muscles following addition of serotonin to 10 μmol/l. Horizontal error bar represents time±SEM to 50% relative response. The time needed to reach each percentile is the mean value from 10 papillary muscles.
FIG. 2 shows the inotropic response to serotonin (10 μmol/l) and isoprenaline (100 μmol/l) in papillary muscles from Chronic heart failure and sham-operated rats. a) Increase in development of force expressed as percent above control. b) Representative examples of single recordings of contraction-relaxation cycles in a papillary muscle exposed to serotonin and isoprenaline. The figure shows representative contractions before addition of agonist (_), at maximal steady state inotropic response to 10 μmol/l serotonin ( - - - - ) and at maximal steady state inotropic response to 100 μmol/l isoprenaline ( . . . . ). Ordinate: Development of tension in arbitrary units. Abscissa: Time after initiating stimulus.
FIG. 3 shows the reversal of the inotropic response to serotonin by cholinergic stimulation. The figure shows the increase in contractile force expressed as percent above control in papillary muscles from Chronic heart failure rats in response to cumulative addition of 10 μmol/l serotonin (5-HT), 30 μmol/l carbachol (CCh) and 1 μmol/l atropine (Atropine). Note that carbachol reversed and atropine restored the inotropic response to serotonin.
FIG. 4 shows the reversal of the inotropic response to serotonin by the 5-HT₄-selective antagonist GR113808. The figure shows representative contraction-relaxation cycles in a papillary muscle from a Chronic heart failure rat before addition of agonist (_), at maximal steady state inotropic response to 10 μmol/l serotonin ( . . . . ) and following reversal by 1 μmol/l GR113808 ( - - - - ). Ordinate: Development of tension in arbitrary units. Abscissa: Time after initiating stimulus.
FIG. 5 shows that the lack of ketanserin effect eliminates involvement of 5-HT_2A-receptors. Concentration-response curves for serotonin in papillary muscles from Chronic heart failure rats in the absence and presence of 0.1 μmol/l ketanserin. Inotropic response was measured as dF/dt and is expressed in percent of maximum in each experiment. The concentration of serotonin needed to reach each percentile was calculated for each experiment according to Ariens and Simonis (1964, Molecular Pharmacology, Vol. 1, New York, Academic Press, 119) and mean values are plotted. Horizontal error bars represent SEM of pEC₅₀values.
FIG. 6 shows that the high affinity of GR 113808 confirms involvement of 5-HT₄-receptors. Concentration-response curves for serotonin in papillary muscles from Chronic heart failure rats in the absence and presence of 0.5 nmol/l GR 113808. The experiments were performed in the presence of 0.1 μmol/l ketanserin and data were analysed and expressed as in FIG. 5.
FIG. 7 shows expression of 5-HT_4(b), 5-HT_2Aand ANP mRNA in left ventricle and papillary muscle of sham treated and CHF rats. Messenger RNA for 5-HT_4(b)receptor (upper panels), 5-HT_2Areceptor (middle panels) and ANP (lower panels) was quantified, and normalised to GAPDH. *CHF vs Sham p<0.01, **CHF vs Sham P<0.05.
FIG. 8 shows the relationship between the maximum inotropic response to 10 μM serotonin in papillary muscle and infarction size (A) and 5-HT₄, 5-HT_2Aand ANP mRNA levels in non-infarcted left ventricle tissue related to infarction size (B).
FIG. 9 shows concentration-response curves for serotonin in papillary muscles of rats 6 weeks after myocardial infarction in the absence and presence of 5 nM SB203186 or 5 nM RS39604. Inotropic response (dF/dt) is expressed in percent of maximum for each papillary muscle.
FIG. 10 shows representative average contraction-relaxation cycles in a papillary muscle from the heart of a rat with CHF 6 weeks after aortic banding before addition of agonist, at maximal steady state inotropic response to 10 μM serotonin, following reversal of the serotonin response with 1 μM GR113808 and at maximal steady state inotropic response to 100 μM isoproterenol.
FIG. 11 shows representative average contraction-relaxation cycles in a trabecular muscle from an explanted human heart before addition of agonist, at maximal steady state inotropic response to 10 μM serotonin, following reversal of the serotonin response with 1 μM GR113808 and at maximal steady state inotropic response to 100 μM isoproterenol.
FIG. 12 shows representative average contraction-relaxation cycles in a trabecular muscle from an explanted human heart before addition of agonist, at maximal steady state inotropic response to 10 μM serotonin, following reversal of the serotonin response with 1 μM GR113808 and at maximal steady state inotropic response to 100 μM isoproterenol.
FIG. 13 shows maximal inotropic response to β adrenoceptor stimulation in rats with CHF treated for six weeks with SB207266 or placebo.

EXAMPLE 1

Animals
Animals were cared for according to the Norwegian Animal Welfare Act which conforms with the Guide for the Care and Use of Laboratory Animals published by the US National Institutes of Health (NIH publication No 85-23, revised 1996). Two rats were kept in each cage and housed in a temperature regulated room with a 12-h day/12-h night cycling and allowed free access to water and food.
Heart Failure Model Induction of Myocardial Infarction
Male, Wistar rats (Møllegaard Breeding and Research Centre, Skensved, Denmark), weighing about 320 g were intubated and ventilated with 68% N₂O, 29% O₂and 2-3% Isofluran (Abbot Laboratories, USA). An extensive myocardial infarction (MI) was induced by a proximal ligation of the left coronary artery. Six weeks later the rats were anaesthetized and ventilated on the respirator with 2.2% Isofluran. Left ventricular pressures were measured (Sjaastad et al., 2000, J. Appl. Physiol, 89: 1445-1454), and Chronic heart failure rats were included in the study if left ventricular end diastolic pressure (LVEDP) was >15 mm Hg. Typically, the infarct comprised most of the left ventricular free wall and also extended to the apex and the base of the papillary muscle. Echocardiography has previously demonstrated severely depressed myocardial function (Sjaastad et al. 200, supra). The sham-operated animals (SHAM) were subjected to the same surgical procedure but the coronary artery was not ligated.
Isolated Papillary Muscles
Hearts were isolated from the anaesthetized animals (see above) and carefully dissected free of connective tissue and transferred to ice cold 0.9% NaCl and weighed. The aorta was cannulated, and the coronaries were perfused at 31° C. with a relaxing solution containing: (mmol/l) NaCl 118.3; KCl 3.0; CaCl₂0.5; MgSO₄4.0; KH₂PO₄2.4; NaHCO₃24.9; glucose 10.0; mannitol 2.2 and equilibrated with 95% O₂/5% CO₂at 31° C. (pH 7.4). Posterior left ventricular papillary muscle was ligated
The muscles were transported to a separate laboratory and mounted in organ baths. In order to prevent contracture of the papillary muscles during transportation and mounting, we used a relaxing solution with a Ca⁺⁺/Mg⁺⁺ concentration ratio of 1:8 comparable to that of St. Thomas' Hospital cardioplegic solution. The papillary muscles were mounted in organ baths containing the relaxing solution and allowed to adapt at 31° C. for about 20 minutes before the solution was changed to one containing the following (in mmol/l): NaCl 119.2; KCJ 3.0; CaCl₂2.0; MgSO₄1.2; KH₂PO₄2.4; NaHCO₃24.9; glucose 10.0; mannitol 2.22 and equilibrated with 95% O₂/5% CO₂at 31° C. (pH 7.4).
The muscles were field stimulated with alternating polarity at 1 Hz with impulses of 5 msec duration and current about 20% above individual threshold (10-15 mA, determined in each experiment). The isometrically contracting muscles were stretched to the maximum of their length-tension curve. The force was recorded and analysed as previously described (Skomedal et al., 1997, J. Pharmacol. Exp. Ther. 280: 721-729). The muscles were allowed to equilibrate for 90 minutes. When used, prazosin (α₁-AR antagonist), timolol (β-AR antagonist), ketanserin (5-HT_2Aselective antagonist) and GR113808 (5-HT₄-selective antagonist) were allowed to act for 90 minutes before addition of agonist. Averaged contraction-relaxation cycles (CRC) were calculated for different experimental periods, and these cycles were used to determine descriptive parameters like maximal development of force (dF/dt)_max, time to peak force (TPF) and time to relaxation to 20% level (TR2O). Relaxation time (RT) was calculated as TR2O−TPF. (dF/dt)_maxwas used as an index of contractility. Inotropic responses induced by agonists were expressed by increase in (dF/dt)_max. RT was used as index of relaxation. Lusitropic responses were expressed as reduction in RT. Mechanical response at the end of the equilibrium period was used as the control response.
Experimental Design
Agonist was added cumulatively or as a single bolus directly to the organ baths and was completely mixed in the solution within 2-3 seconds. The concentration-dependent inotropic and lusitropic responses to 5-HT₄-receptor stimulation by serotonin were obtained in the presence of prazosin (1 μmol/l) and timolol (3 μmol/l or 1 μmol/l) atropine (1 μmol/l) and ascorbate (10 μmol/l), respectively. Concentration-response curves for serotonin were obtained by adding serotonin cumulatively in the absence and presence of ketanserin (0.1 μmol/l). Concentration-response curves for 5-HT₄-receptor stimulation in the presence of ketanserin were performed in the absence and presence of 0.5 nmol/l GR113808 and the relative shift of the curves was used to calculate the K_bfor GR113808. When serotonin was added as a single dose (10 μmol/l) the experiments were performed in the absence of ketanserin. The presence of either antagonist did not influence the basal or maximal function of the muscles with regard to mechanical performance or electrical stimulation threshold (data not shown). The different agonists were added directly to the organ baths in increasing concentrations until supramaximal concentrations of agonist were obtained with respect to maximal inotropic response.
Calculation and Statistics
The responses for each concentration of agonist were generally calculated as percent of maximal response. The concentration-response curves constructed from papillary muscle experiment were constructed according to Ariens and Simonis (1964, supra), by estimating centiles (EC₁₀to EC₁₀₀) for each single experiment and calculating the corresponding means. This calculation provides mean curves that express the response as fractional response or percent of maximum and display horizontal positioning and the correct mean slope of the curves. The horizontal positioning of the concentration-response curves was expressed as pEC₅₀-values (=−logEC₅₀). Data are expressed as mean±standard error of the mean (SEM) and the number of animals expressed as n. The significance levels of differences were calculated according to Students t-test. P<0.05 is considered statistically significant. The inhibition constants K_bwere calculated from the Schild equation, based on the relative shifts of the concentration-response curves for receptor stimulation.
Drugs
Serotonin (5-hydroxytryptamine hydrochloride, 5-HT) was from Sigma (St. Louis, Mo., USA). GR 113808 ({1-[2-(methyl-sulphonylamino)ethyl]4-piperidinyl}methyl 1-methyl-1H-indole-3-carboxylate) maleate was from Tocris (Bristol, UK). Ketanserin (3-[2-[4-(4-fluorobenzoyl)-1-piperidinyl]ethyl]-2,4(1H,3H)-quinazolinedione) tartrate was from RBI (Natick, Mass., USA). Prazosin hydrochloride, timolol maleate. (−)-isoprenaline hemisulphate, ascorbate, carbamylcholine (carbachol) and atropine sulfate were purchased from Sigma. Stock solutions were prepared in double destilled water and kept at minus 20° C. to avoid oxidation. Further dilutions of the drugs were made fresh daily and kept cool (0-4° C.).
Results
Inotropic Effects of Serotonin in Heart Failure Rats
In the presence of prazosin, atropine and timolol 10 μmol/l of serotonin elicited a monophasic positive inotropic response not seen in sham-operated animals (n=6) (FIG. 1, 2 a). With a lag phase (diffusion delay) of about 5 seconds the time from addition of serotonin to 50% relative inotropic response was 22±2.0 sec, and to maximal inotropic response 1-2 minutes (FIG. 1, inset). The serotonin mediated increase in contractile force in papillary muscles from post-MI heart failure rats was 44.5±2.9% (SEM, n=10), comparable to the inotropic effect of 10 μmol/l isoprenaline 60.4±5.8% (or 58.5±7%) (SEM, n=10) (FIG. 2 a). The inotropic responses through the respective receptors were not additive indicating coupling to the same signalling pathway. In sham-operated animals, however, isoprenaline evoked a positive inotropic response of 111.6±8.6% (mean±SEM, n=6) (FIG. 2 a) underlining the attenuation of the mechanical response to β-adrenoceptor stimulation in failing myocardium.
Qualitative Characteristics of the Inotropic Response to Serotonin
The inotropic response to serotonin induced qualitative changes in the contraction-relaxation cycles (FIG. 2 b) not observed in sham-operated animals. Time to peak force in the control period was 148.0±3.9 ms (mean±SEM, n=8) and after stimulation by serotonin there was a shortening of the contraction-relaxation cycles with a significant reduction in TPF, TR2O and RT (table 1). These changes reflect a selective increase in relaxation compared to contraction, which is comparable to what is observed during β-adrenoceptor stimulation in myocardial preparations (Skomedal et al. 1997, supra), and consistent with common signalling pathways for these agents.
Influence of Cholinergic Stimulation on the Inotropic Response Induced by Serotonin
Stimulation of muscarinic acetylcholine receptors is well known to exert a functional antagonism of inotropic effects mediated through G_αs-adenylyl cyclase-pathway and as a pharmacological approach to elucidate the involvement of such a pathway in the serotonin induced inotropic response we stimulated these receptors with carbachol. 10 μmol/l of serotonin exerted a positive inotropic response of 33.7±6.6% (mean±SEM, n=5) above control level. Carbachol (30 μmol/l) reversed the response to 4.8±6.5% (mean±SEM, p<0.01) within 2-3 seconds (or 1-2 minutes) (FIG. 3) and partially reversed TPF, TR2O and RT. Atropine (1 μmol/l) restored the response to 45.1±5.1% (mean±SEM, p>0.06 vs. serotonin alone, 2-tailed paired t-test) and re-established the contraction-relaxation cycle characteristics, suggesting an involvement of the G_αs-adenylyl cyclase-pathway.
Reversal of the Inotropic Response Induced by Serotonin by the 5-HT-Selective Antagonist GR113808
The qualitative characteristics of the inotropic response to serotonin, its similarity to the inotropic response to isoprenaline and the reversal by carbachol all indicated an involvement of the G_s-adenylyl cyclase-pathway. Three different serotonin-receptors couple to G_sand stimulation of adenylyl cyclase, 5-HT₄, 5-HT₆and 5-HT₇(Hoyer et al., 1994, Pharmacol. Rev. 46: 157-203). Of these, the 5-HT₄receptor is known to mediate inotropic and chronotropic effects in human and porcine atrium (Kaumann, 1994, Trends Pharmacol. Sci. 15: 451-455), albeit not in rat (Läer et al., 1998, Br. J. Pharmacol. 123: 1182-1188). We therefore tested whether a 5-HT₄-selective serotonin receptor antagonist would block the serotonin-mediated inotropic response in papillary muscle from Chronic heart failure rats. GR113808 is a selective 5-HT₄-antagonist with a pKi of 9.2-9.7 (Gale et al., 1994, Br. J. Pharmacol. 111: 332-338), and 1 μmol/l GR113808 completely reversed the inotropic response evoked by 10 μmol/l serotonin (FIG. 4). The shortening of the contraction-relaxation cycles induced by serotonin was also sensitive to GR113808. However, as seen from FIG. 4, these serotonin-induced changes were not completely reversed when GR113808 was given subsequent to serotonin. This is a typical finding with cAMP-mediated stimulation of inotropy (Skomedal et al., 1997, supra), and does not detract from the fact that GR113808 was able to fully reverse the effects of serotonin.
Lack of Ketanserin Effect Eliminates Involvement of 5-HT_2AReceptors
To the extent that inotropic effects of serotonin have been demonstrated in the rat heart, these have been confined to the atrium and have been mediated by 5-HT_2A-receptors (Laer et al., 1998, supra). To test whether 5-HT₂-receptors could also be involved in the inotropic effect of serotonin in papillary muscle from Chronic heart failure rats, we used the 5-HT_2Areceptor antagonist ketanserin. Ketanserin (0.1 μmol/l) did not shift the concentration-response curve for serotonin to higher concentrations of agonist (pD₂-value with ketanserin 7.49±0.08 (SEM, n=5) vs. 7.62±0.06 (SEM, n=6) without, p=0.24, unpaired Students t-test), suggesting that the 5-HT_2A-receptor is not involved in the inotropic response to serotonin in papillary muscles from post-MI Chronic heart failure rats (FIG. 5). There was no significant difference between the maximal inotropic responses in the two groups (with and without ketanserin), measured at the top of each concentration-response curve (pooled result 17.5±1.9% (SEM, n=11)). The apparently lower inotropic effect in this experiment compared to that in e.g. FIG. 2 a illustrates a consistently lower inotropic effect in all experiments when measured after a full concentration-response curve as opposed to a direct stimulation with a high concentration (e.g. 10 μmol/l) of serotonin. This difference may reflect desensitisation of the response during the continuous stimulation with increasing concentrations of serotonin, as is done to achieve the concentration-response curves.
High Affinity of GR113808 Documents Involvement of 5-HT₄Receptors

To provide pharmacological evidence for the involvement of 5-HT₄receptors, the shift of the concentration-response curve to serotonin by GR113808 was determined. The experiment was performed in the presence of 0.1 μmol/l ketanserin to block 5-HT_2Areceptors, if present. The concentration-response curves to serotonin in the absence and presence of 0.5 nmol/l GR113808 were essentially parallel with pEC₅₀-values of 7.62±0.06 (SEM, n=6) and 7.32±0.06 (SEM, n=6, p<0.005), respectively (FIG. 6), with no difference in the maximum inotropic response induced by serotonin between the groups (pooled average 18.7±2.4% (SEM, n=12)). The corresponding GR113808 inhibition constant (K_b) calculated from the Schild equation was 0.5 nmol/l, corresponding to a pK_bvalue of 9.3. Since GR113808 displays at least 1000-fold selectivity for the 5-HT₄receptor over all other known receptors, this provides strong evidence for a 5-HT₄receptor-mediated inotropic response to serotonin in papillary muscle from Chronic heart failure rats.

TABLE 1


Qualitative characteristics of the contraction-
relaxation cycles (CRC) in Chronic heart failure and
sham-operated animals before and after subsequent
addition of serotonin (10 μmol/l) and isoprenaline (100 μmol/l),
respectively.

Control	5-HT	5-HT	ISO	Iso
(ms)	(ms)	(% of control)	(ms)	(% of control)

	Sham
	n = 6

TPF	125.1 ± 5.5	123.7 ± 5.5	99.0 ± 0.8	109.3 ± 2.7	87.4 ± 2.3
TR20	233.6 ± 11.2	231.0 ± 11.0	99.0 ± 0.7	174.0 ± 4.9	74.5 ± 1.7
RT (TR20 − TPF)	108.4 ± 6.2	107.3 ± 5.9	99.0 ± 0.5	75.0 ± 2.5	69.4 ± 3.2

	CHF
	n = 10

TPF	148 ± 3.9	134 ± 3.5	90.5 ± 1.4	123.1 ± 1.6	83.2 ± 1.7
TR20	254.3 ± 6.3	224.6 ± 5.4	88.3 ± 1.5	204.1 ± 2.9	80.3 ± 1.9
RT (TR20 − TPF)	106.3 ± 2.5	90.6 ± 2.2	85.2 ± 1.5	81.0 ± 1.8	76.2 ± 1.8

Values are mean ± SEM of average results from 20-40 CRC in each group of papillary muscles.
TPF = Time to peak force
TR2O = Time to relaxation to 20% level
RT = Relaxation time

EXAMPLE 2

Quantitative Reverse Transcriptase Polymerase Chain Reaction (RT-PCR) to Examine 5-HT₄Receptor mRNA Induction in CHF
Non-infarcted left ventricle tissue (30-50 mg, mainly septum), collected immediately after removal of the papillary muscle, or papillary muscle (15-30 mg including some left ventricular wall) collected after completion of functional analyses, stored in RNAlater (Ambion) until use, was flash frozen and reduced to powder under liquid nitrogen. Total RNA was isolated from tissue powder homogenized in 1 ml TRIZOL (Invitrogen), followed by mRNA extraction (Bach et al. 2001 supra) and oligo-dT-primed first strand cDNA synthesis (Medhurst et al. 2001 Brain Res Mol Brain Res 90: 125-134). A standard curve with 5-300 ng mRNA was made to control for reverse transcription and PCR quantification.
Sets of primers (targeted to intron/exon boundaries to avoid genomic DNA signals) and probes (Double-Dye Oligonucleotide, Eurogentec, 5′-labeled with the fluorescent reporter dyes FAM (5-HT_4(b), GI:924649 (Gerald et al. 1995 EMBO J. 14: 2806-2815) and 5-HT_2A, GI:207067 (Julius et al. 1990 PNAS USA 87: 928-932)), JOE (Eurogentec; glyceraldehyde-3-phosphate dehydrogenase (GAPDH; GI:10190788)) or Yakima Yellow (YY; Eurogentec; atrial natriuretic peptide (ANP; GI:55711)) and quenched with TAMRA (5-HT_4(b), 5-HT_2Aand GAPDH) or Dark Quencher (DQ; Eurogentec; ANP)) for quantitative PCR were designed as described (Bustin et al. 2000 J. Mol Endocrinol 25: 169-193). The names and sequences of upper (U) and lower (L) primers and probes (P) used were (5′-3′): 5-HT_4(b): ON283(U), CATGTGCATAGGTATACAGTGGAATGT; ON284 (L), GCAGCCACCAAAGGAGAAGTT; TM14(P), FAM-CCATCTGCTGCCAGCCTTTGGTCTATAGGA-TAMRA; 5-HT_2A: ON273(U); TTCACCACAGCCGCTTCAA; ON274(L), ATCCTGTAGTCCAAAGACTGGGATT; TM9(P), FAM-ATGGATATACCTACAGATATGGTCGTCCACACGGCAAT-TAMRA; ANP: ON285(U), ATCTGATGGATTTCAAGAACC; ON286(L), CTCTGAGACGGGTTGACTTC; TM15(P) YY-CGCTTCATCGGTCTGCTCGCTCA-DQ; GAPDH: ON279(U), CCTGCACCACCAACTGCTTA; ON290(L), GGCATGGACTGTGGTCATGA; TM12(P), JOE-TGGCCAAGGTCATCCATGACAACTTTG-TAMRA.
Quantitative RT-PCR (Medhurst et al. supra) was done in 25 μl reactions with TaqMan Universal PCR Master Mix (Applied Biosystems) containing 5 mM Mg²⁺, 300 nM of each primer, 200 nM probe and long template cDNA. GAPDH was quantified separately for normalization with 0.1 ng cDNA template. Raw data were collected and analyzed with Sequence Detector Software (SDS version 1.7; Applied Biosystems) (Bustin et al. 2000, supra). Results are expressed as mean±SEM from n animals. P<0.05 was considered statistically significant (nonparametric Mann-Whitney test).
Induction of 5-HT_4(b)Receptor mRNA in CHF
Quantitative RT-PCR was used to determine the level of mRNA encoding 5-HT_4(b)receptor, 5-HT_2Areceptor, and the heart failure marker ANP normalized to the level of GAPDH mRNA. In left ventricle and papillary muscle, respectively, 5-HT_4(b)mRNA levels were four and 18-fold higher in CHF vs. Sham, whereas 5-HT_2AmRNA levels were unchanged and ANP mRNA levels increased (FIG. 7). The ratio between normalized 5-HT_4(b)and 5-HT_2AmRNA levels was increased in CHF in both left ventricle and papillary muscle, confirming increased 5-HT_4(b)mRNA level relative to 5-HT_2A, independent of GAPDH (Table 2).

EXAMPLE 3

The Maximum Inotropic Response to Serotonin and 5-HT_4(b)Receptor mRNA Related to Infarction Size.

In papillary muscles from MI_nfrats i.e. rats in which symptoms of CHF were not obtained, despite having undergone surgery to induce myocardial infarction, serotonin (10 μM) elicited an inotropic response qualitatively similar to the response observed in CHF animals. The magnitude of the response correlated positively with infarction size up to 30-40% of the inner myocardial surface in MI_nfanimals (FIG. 8A). In MI_nfhearts with infarct size 30-40% the inotropic effect was of the same magnitude as in CHF hearts which all had infarct size >40%. A positive correlation with infarction size was also observed for 5-HT_4(b)and ANP mRNA expression, whereas 5-HT_2AmRNA levels were unchanged (FIG. 8B). These findings suggest a gradual transition related to the extent of myocardial changes secondary to the infarction.

TABLE 2


Ratio of 5-HT_4(b)receptor mRNA to 5-HT_2Areceptor mRNA

	Sham	CHF

Left ventricle	0.87 ± 0.33 (n = 7)	3.20 ± 1.09 (n = 11)*
Papillary muscle	0.85 ± 0.64 (n = 4)	7.48 ± 2.44 (n = 5)†

To test the observation of increased 5-HT_4(b)receptor level independent of GAPDH the ratio of normalized 5-HT_4(b)receptor mRNA to normalized 5-HT_2Areceptor mRNA was calculated.
*CHF vs. Sham p < 0.06;
†CHF vs. Sham p < 0.05

EXAMPLE 4

The inotropic response to serotonin in papillary muscle from 6 week post myocardial infarction rats was measured in the presence of several chemically different 5-HT₄receptor antagonists, as described above.
The 5-HT₄antagonists SB203186 and RS39604, each added at 5 nM, block the inotropic response to serotonin in 6 week post MI rats with blocking potencies corresponding to their known affinities at 5-HT₄receptors. The figure shows concentration-response curves for serotonin in papillary muscles of rats 6 weeks after myocardial infarction in the absence and presence of 5 nM SB203186 or 5 nM RS39604. Inotropic response (dF/dt) is expressed in percent of maximum for each papillary muscle.
The pEC₅₀value for serotonin in the absence of blocker was 7.25±0.2. The pEC₅₀value for serotonin in the presence of 5 nM SB203186 was 6.39, corresponding to a pK_bvalue of 9.1. The pEC₅₀value for serotonin in the presence of 5 nM RS39604 was 6.26, corresponding to a pK_bvalue of 9.2. This is consistent with the inotropic response to serotonin being mediated via 5-HT₄receptors.

EXAMPLE 5

5-HT₄Receptor-Mediated Inotropic Responses in Rat Hypertensive Heart Failure
A second model of heart failure was then used to study the 5-HT₄receptor-mediated inotropic effect of serotonin; namely a model of rat hypertensive heart failure. This study uses a rat model of heart failure obtained by aortic banding. In this model, the heart failure is induced by a constantly increased afterload, somewhat reminiscent of human hypertensive heart failure. This study was performed to clarify whether it is the heart failure as such, or the cardiac infarction preceding the heart failure that underlies the induction of 5-HT₄receptors in the post-infarction model.
Trans-aortic constriction (aortic banding) of the ascending aorta was induced in 200 g male Wistar rats under anaesthesia, induced by 63% N₂O, 32% O₂and 5% Isoflurane and maintained by 66% N₂O, 33% O₂and 1-2% Isoflurane. A right-sided thoracotomi was performed through a 3-4 cm long cutaneous incision, the pericardium was opened and the ascending aorta identified and dissected free of surrounding tissue. A ligature was knit around the ascending aorta and a metal probe with diameter 0.9 mm. The metal probe was then removed. The result was a constriction of the ascending aorta with internal diameter about 0.9 mm. The thorax was then closed with 3-0 silk sutures and the skin closed with Dexon 1 sutures. The animals received post-operative analgesia with buprenorphine 0.09 mg subcutaneously and were allowed to wake up in a 30° C. environment. After six weeks the animals were again placed under anaesthesia as during the primary surgery, and an echocardiographic examination was performed. Finally the thorax was opened and the heart was removed for preparation of posterior left ventricular papillary muscles as described (Sjaastad et al. 2003 Acta physiol Scand 177: 449-458). The rat was considered to have CHF.
Papillary muscle was extracted from a CHF rat 6 weeks after aortic banding as described above. Posterior left ventricular papillary muscle was prepared, mounted in organ bath, equilibrated and field stimulated at 1 Hz (Sjaastad et al. 2003 supra), and the contraction-relaxation cycles (CRCs) were recorded and analysed as previously described (Skomedal et al. 1997, J. Pharmacol Exp Ther 280: 721-729) (Sjaastad et al., 2003, supra) with respect to maximal developed force (F_max), maximal development of force (dF/dt)_max, time to peak force (TPF), time to relaxation to 20% level (TR20) and relaxation time (RT=TR20−TPF). The experiment was performed in the presence of blockers (added 90 min prior to serotonin) of adrenergic and muscarinic cholinergic receptors (prazosin 1 μM, timolol 1 μM, atropine 1 μM).
FIG. 10 shows representative average contraction-relaxation cycles in a papillary muscle from the heart of a rat with CHF 6 weeks after aortic banding before addition of agonist, at maximal steady state inotropic response to 10 μM serotonin, following reversal of the serotonin response with 1 μM GR113808 and at maximal steady state inotropic response to 100 μM isoproterenol. Serotonin (10 μM) elicited a positive inotropic response comparable in magnitude and characteristics to the positive inotropic response to 100 μM isoproterenol (enough to surmount the blockade by 1 μM timolol). The positive inotropic response to serotonin was reversed by 1 μM of the 5-HT₄antagonist GR113808, indicating that the response is mediated through 5-HT₄receptors.
This shows that this model of heart failure in rats also causes the appearance of a 5-HT₄receptor-mediated inotropic response to serotonin, indicating that this finding is general for heart failure as such, at least in rats.

EXAMPLE 6

5-HT₄Receptor-Mediated Inotropic Effect of Serotonin in Human Heart
To study the 5-HT₄receptor-mediated inotropic response to serotonin in human heart, trabecular muscle from a post-infarct human heart and a human heart with heart failure due to dilated cardiomyopathy was used.
FIG. 11 shows representative average contraction-relaxation cycles in a trabecular muscle from the explanted post infarct human heart before addition of agonist, at maximal steady state inotropic response to 10 μM serotonin, following reversal of the serotonin response with 1 μM GR113808 and at maximal steady state inotropic response to 100 μM isoproterenol.
The heart was explanted from a patient who had survived a small myocardial infarction and died in hospital from subarachnoidal haemorrhage. Trabecular muscles were prepared, mounted in organ baths, equilibrated and field stimulated at 1 Hz (Skomedal et al., 1997, supra) and the contraction-relaxation cycles (CRCs) were recorded and analysed as previously described (Skomedal et al., 1997, supra) with respect to maximal developed force (F_max), maximal development of force (dF/dt)_max, time to peak force (TPF), time to relaxation to 20% level (TR20) and relaxation time (RT=TR20−TPF). The experiment was performed in the presence of blockers (added 90 min prior to serotonin) of adrenergic and muscarinic cholinergic receptors (prazosin 1 μM, timolol 1 μM, atropine 1 μM).
As seen in FIG. 11, serotonin (10 μM) elicited a positive inotropic response amounting to about 10% of the positive inotropic response to 100 μM isoproterenol (enough to surmount the blockade by 1 μM timolol). The positive inotropic response to serotonin was reversed by 1 μM of the 5-HT₄receptor antagonist GR113808, indicating that the response is mediated through 5-HT₄receptors.
A heart was also explanted from a patient who had received a heart transplant due to heart failure from dilated cardiomyopathy. Trabecular muscles were prepared and the contraction-relaxation cycles (CRCs) were recorded and analysed as described above. In addition to the presence of blockers as above, the positive inotropic responses to serotonin and isoproterenol were enhanced by the presence of the phosphodiesterase inhibitor IBMX (isobutyl-methyl-xanthine; 35 μM).
FIG. 12 shows representative average contraction-relaxation cycles in a trabecular muscle from this explanted human heart before addition of agonist, at maximal steady state inotropic response to 10 μM serotonin, following reversal of the serotonin response with 1 μM GR113808 and at maximal steady state inotropic response to 100 μM isoproterenol.
As seen in the figure, serotonin (10 μM) elicited a positive inotropic response amounting to about 32% of the positive inotropic response to 100 μM isoproterenol (enough to surmount the blockade by 1 μM timolol). The positive inotropic response to serotonin was reversed by 1 μM of the 5-HT₄receptor antagonist GR113808, indicating that the response is mediated through 5-HT₄receptors.
This shows that the presence of an inotropic response through 5-HT₄receptors in the failing heart is also seen in humans.

EXAMPLE 7

Effect of Treatment of Post-Infarction Congestive Heart Failure (CHF) Rats with a 5-HT₄Antagonist.
An extensive myocardial infarction (MI) was induced in 320 g male Wistar rats under anaesthesia (68% N₂O, 29% O₂and 2-3% Isofluran) by a proximal ligation of the left coronary artery (Sjaastad et al. 2003, supra). Three days later, rats were included in the study if the rats had both clinical signs of congestive heart failure (tachypnoe and forced ventilation) and a large myocardial infarction as verified by echocardiography. Rats included in the study were randomized blindly to placebo or treatment.
Under anesthesia with 75 μg/kg Fentanyl (Janssen Pharmaceutical) and 3.75 mg/kg Midazolam (Roche) s.c., as well as local anesthesia with Xylocaln 1% around the incision, the rats received subcutaneous implantation of 2 ml Alzet miniosmotic pumps (Alza, Palo Alto, Calif.) containing solvent (100 μM ascorbic acid, 50 μM EDTA in water; placebo group) or solvent containing 50 mM of the 5-HT₄antagonist SB207266 (treatment group). The pumps were replaced with new pumps after three weeks to obtain a total treatment time of six weeks.
After six weeks of treatment, the animals were again placed under Isofluran anaesthesia (68% N₂O, 29% O₂and 2-3% Isofluran) with temperature control for echocardiographic and hemodynamic measurements, followed by euthanasia. Posterior left ventricular papillary muscles were then prepared, mounted in organ baths, equilibrated and field stimulated at 1 Hz (Sjaastad et al., 2003 supra) and the contraction-relaxation cycles (CRCs) were recorded and analysed as previously described with respect to maximal developed force (F_max), maximal development of force (dF/dt)_max, time to peak force (TPF), time to relaxation to 20% level (TR20) and relaxation time (RT=TR20−TPF).
The experiments were performed in the presence of blockers (added 90 min prior to agonist) of α-adrenergic and muscarinic cholinergic receptors (prazosin 1 μM, atropine 1 μM). Isoproterenol was added to the organ bath cumulatively and the maximal positive inotropic response to isoproterenol was calculated for each animal.
The results are shown in FIG. 13 and indicate a trend towards normalisation of myocardial function, as judged by the trend towards normalisation of the CHF-induced reduction of maximal inotropic response to β-adrenoceptor stimulation, by treatment with the 5-HT₄antagonist SB207266.
Furthermore, in CHF, the duration of the contraction-relaxation cycle is prolonged, due to changes in myofilament composition. Therefore, the duration of the contraction-relaxation cycle can be used as an additional parameter of the degree of myocardial dysfunction. Our preliminary data from treatment with the 5-HT₄antagonist SB207266 also show a trend towards normalisation of this parameter of myocardial dysfunction (data not shown).

EXAMPLE 8

Tablets (Oral) for Treatment and Prophylaxis of Heart Failure

GR113808 (as hydrochloride salt) 10.95 g

lactose 157 g

microcrystalline cellulose 30 g

magnesium stearate BP 2.05 g
The active ingredients are passed through a 24 mesh sieve and blended with lactose, microcrystalline cellulose and magnesium stearate. The resulting mixture is pressed into tablets. Tablet weight is 200 mg and each tablet contains 10 mg GR113808.

EXAMPLE 9

Capsules (Oral) for Treatment and Prophylaxis of Heart Failure

SB207266(as hydrochloride salt) 5.5 g

Atenolol 25 g

lactose 169.5 g
The active ingredients are passed through a 24 mesh sieve and blended with lactose. The mixture is filled into gelatin capsules (200 mg) using suitable machinery. Each capsule contains 5 mg SB207266 and 50 mg atenolol.

EXAMPLE 10

Solution for Injection for Treatment and Prophylaxis of Heart Failure

SB207266(as hydrochloride salt) 10.9 g

sodium chloride q.s.

water for injection ad. 10 litre
SB207266 (as hydrochloride salt) and sodium chloride are dissolved in water for injection to form an isotonic solution. The mixture is filled into vials (10 ml) with rubber stoppers and sterilised by heating in an autoclave for 20 minutes at 121 degrees centrigade. Each vial contains 10 ml and 1 mg SB207266 per ml.

EXAMPLE 11

Capsules (Oral) for Treatment and Prophylaxis of Heart Failure

SB207266(as hydrochloride salt) 5.5 g

metoprolol tartrate 50 g

lactose 144.5 g
The active ingredients are passed through a 24 mesh sieve and blended with lactose. The mixture is filled into gelatin capsules (200 mg) using suitable machinery. Each capsule contains 5 mg SB207266 and 50 mg metoprolol tartrate.

EXAMPLE 12

Capsules (Oral) for Treatment and Prophylaxis of Heart Failure

SB207266(as hydrochloride salt) 5.5 g

enalapril maleate 10 g

lactose 184.5 g
The active ingredients are passed through a 24 mesh sieve and blended with lactose. The mixture is filled into gelatin capsules (200 mg) using suitable machinery. Each capsule contains 5 mg SB207266 and 10 mg enalapril maleate.

EXAMPLE 13

Capsules (Oral) for Treatment and Prophylaxis of Heart Failure

SB207266(as hydrochloride salt) 5.5 g

losartan potassium 50 g

lactose 169.5 g
The active ingredients are passed through a 24 mesh sieve and blended with lactose. The mixture are filled into gelatin capsules (200 mg) using suitable machinery. Each capsule contains 5 mg SB207266 and 50 mg losartan potassium salt.

EXAMPLE 14

Capsules (Oral) for Treatment and Prophylaxis of Heart Failure (5HT-₄Receptor Antagonist Plus α/β-Blocker)

SB207266(as hydrochloride salt) 5.5 g

carvedilol 12.5 g

lactose 182 g
The active ingredients are passed through a 24 mesh sieve and blended with lactose. The mixture is filled into gelatin capsules (200 mg) using suitable machinery. Each capsule contains 5 mg SB207266 and 12.5 mg carvedilol.

EXAMPLE 15

Suppositories for Treatment and Prophylaxis of Heart Failure

GR113808(as hydrochloride salt) 16.5 g

Glyceride mixture of fatty acid 193.5 g
GR113808 salt is milled down to a particle size of approximately 20 microns. A suspension of the salt is prepared in molten glyceride of fatty acid and filled into suppository moulds. The weight of each suppository is 200 mg with unit dose of 15 mg GR113808.

Claims

1. A method for treating or preventing heart failure in a mammal comprising administering to said mammal a pharmaceutically effective amount of a 5-HT₄receptor antagonist.

2. The method of claim 1 wherein the treatment or prevention of atrial arrhythmia is excluded.

3. The method of claim 1 wherein said heart failure is characterised by impaired cardiac function due to systolic or diastolic dysfunction.

4. The method of claim 1 wherein said heart failure is chronic heart failure.

5. The method of claim 1 wherein said heart failure is congestive heart failure.

6. The method of claim 5 wherein said congestive heart failure is chronic congestive heart failure.

7. The method of claim 1 wherein said heart failure results from ischaemic heart disease, or chronic non-ischaemic cardiomyopathy (IDCM), or cardiomyopathy due to hypertension.

8. The method of claim 1 wherein said heart failure is post-infarction heart failure.

9. The method of claim 1 wherein said 5-HT₄receptor antagonist inhibits the inotropic response of the heart to 5-HT.

10. The method of claim 1 wherein said 5-HT₄receptor antagonist is selected from compounds comprising an aromatic ring structure with a hydrogen-bond acceptor as one substituent and a hydrogen-bond acceptor as a second substituent and a tertiary amine spaced with at least three bonds away from the aromatic ring.

11. The method of claim 1 wherein said 5-HT₄receptor antagonist comprises an aromatic ring to which a carbonyl group is attached, and a basic nitrogen in an appended side chain and an oxygen atom adjacent to the carbonyl group.

12. The method of claim 1, wherein said 5-HT₄receptor antagonist is selected from the group consisting of benzoate esters, benzoate amides, imidazolopyridines, aryl ketones, indoles, carbazimidamides, phenylcarbamates and phenylureas.

13. The method of claim 1 wherein said 5-HT₄receptor antagonist is selected from the group consisting of 1-piperidinyl-ethyl-1H-indole-3-carboxylate, SB203186; (1 butyl 4 piperidinyl)methyl 8 amino 7 iodo-1,4 benzodioxan 5 carboxylate, SB207710; [1 [2 methylsulphonylamino ethyl] 4-piperidinyl]-methyl]methyl 1H indole 3 carboxylate, GR113808; 2 diethylaminoethyl (2 methoxy 4 amino 5 chloro)benzoate, SDZ205557; endo 8 methyl 8 azabicyclo[3.2.1]oct 3 yl 2,3 dihydro 6 methoxy 2 oxo 1H benzimidazole 1 carboxylate, DAU 6285; 1 [4 amino 5 chloro 2 (3,5 dimethoxybenzyl-oxy)phenyl] 3[1 [2 [(methylsulfonyl)amino]ethyl] 4 piperidinyl] 1 propanone hydrochloride, RS 39604; (1 n butyl 4 piperidinyl)methyl 8 amino 7 chloro 1,4 benzodioxane 5 carboxylate, SB 204070; N [(1 butyl 4 piperidinyl)-methyl] 3,4dihydro 2H [1,3]oxazino[3,2 a]indole10-carboxamide hydrochloride, SB 207266; (endo 3,9 dimethyl 3,9 diazabicyclo[3,3,1]non 7 yl 1H indazole 3 carboxamide dihydrochloride), N 3389; [(+) 8,9 dihydro 10 methyl 7 [(5 methyl 4 imidazolyl)methyl]pyrido [1,2 a] indole 6(7H) one hydrochloride], FK1052; 2 (cis 3,5 dimethyl-piperidino)ethyl 4 amino 5 chloro 2 methoxybenzoate, ML10375; [3 (piperidine 1 yl)propyl 4 amino 5 chloro 2 methoxybenzoate hydrochloride], RS 23597 190; (1-[2-[(methyl-sulphonyl)amino]-ethyl]-4-piperidinyl-methyl-5-fluoro-2-methoxy-1H-indole-3-carboxylate), GR125487; R50595 (FR76530); RS100302; 1-(1-methylethyl)-N-[2-[4-[tricyclo[3.3.1.1 (3,7)]dec-1-ylcarbonyl)amino]-1-piperidinyl]ethyl-1H-indazole-3-carboxamide, LY353433; A-85380; SB205800; SB 207058; SB 207226; SC-53606 and SC 56184.

14. The method of claim 1 wherein said 5-HT₄receptor antagonist is an antibody or fragment or derivative thereof.

15. The method of claim 1 wherein said 5-HT₄receptor antagonist is formulated as a physiologically acceptable salt.

16. The method of claim 1 wherein said 5-HT₄receptor antagonist is formulated for oral administration or parenteral administration.

17. The method of claim 1 wherein the 5-HT₄receptor antagonist blocks a response to 5-HT.

18. (canceled)

19. The method of claim 1, wherein said mammal does not have atrial arrhythmia.

20. The method of claim 1 wherein cardiac performance is improved.

21. The method of claim 20 wherein ventricular ejection fraction is increased.

22. The method of claim 21 wherein left ventricular ejection fraction is increased.

23. The method of claim 20 wherein the improvement in cardiac performance is one or more of the following: New York Heart Association (NYHA) functional class is reduced, exercise capacity is improved, pulmonary capillary wedge pressure is decreased, peak heart rate is increased, peak systolic blood pressure is increased and neutral velocity deceleration time is increased.

24. The method of claim 1 wherein the plasma level of Nt-proANP is reduced.

25. A pharmaceutical composition comprising a 5-HT₄receptor antagonist and a pharmaceutically acceptable carrier diluent or excipient, wherein said 5-HT₄receptor antagonist is present in said composition in an amount sufficient for the treatment or prevention of heart failure.

26. The pharmaceutical composition of claim 25 further comprising a second agent effective for the treatment of heart failure.

27. A composition comprising

(a) a 5-HT₄receptor antagonist, and

(b) a second agent effective for the treatment of heart failure as a combined preparation for simultaneous, separate or sequential use in the treatment of heart failure or in improving cardiac function.

28. The pharmaceutical composition of claims 26 or 27 wherein said second agent is selected from the group consisting of diuretics, vasodilators, inotropic drugs, anticoagulants, β blockers, angiotension II blockers and angiotension converting enzyme inhibitors.

29. The pharmaceutical composition of claim 28 wherein said second agent is a β blocker.

30. The method of claim 7, wherein said ischaemic heart failure is a chronic ischaemic heart failure.

31. The method of claim 7, wherein said chronic non-ischaemic cardiomyopathy is idiopathic dilated cardiomyopathy.

32. The pharmaceutical composition of claim 25, wherein said 5-HT₄receptor antagonist is selected from compounds comprising an aromatic ring structure with a hydrogen-bond acceptor as one substituent and a hydrogen-bond acceptor as a second substituent and a tertiary amine spaced with at least three bonds away from the aromatic ring.

33. The pharmaceutical composition of claim 25, wherein said 5-HT₄receptor antagonist comprises an aromatic ring to which a carbonyl group is attached, and a basic nitrogen in an appended side chain and an oxygen atom adjacent to the carbonyl group.

34. The pharmaceutical composition of claim 25, wherein said 5-HT₄receptor antagonist is selected from the group consisting of benzoate esters, benzoate amides, imidazolopyridines, aryl ketones, indoles, carbazimidamides, phenylcarbamates and phenylureas.

35. The pharmaceutical composition of claim 25, wherein said 5HT₄receptor antagonist is selected from the group consisting of 1-piperidinyl-ethyl-1H-indole-3-carboxylate, SB203186; (1 butyl 4 piperidinyl)methyl 8 amino 7 iodo-1,4 benzodioxan 5 carboxylate, SB207710; [1 [2 methylsulphonylamino ethyl] 4-piperidinyl]-methyl]methyl 1H indole 3 carboxylate, GR113808; 2 diethylaminoethyl (2 methoxy 4 amino 5 chloro)benzoate, SDZ205557; endo 8 methyl 8 azabicyclo[3.2.1]oct 3 yl 2,3 dihydro 6 methoxy 2 oxo 1H benzimidazole 1 carboxylate, DAU 6285; 1 [4 amino 5 chloro 2 (3,5 dimethoxybenzyloxy)phenyl] 3[1 [2 [(methylsulfonyl)amino]ethyl] 4 piperidinyl] 1 propanone hydrochloride, RS 39604; (1 n butyl 4 piperidinyl)methyl 8 amino 7 chloro 1,4 benzodioxane 5 carboxylate, SB 204070; N [(1 butyl 4 piperidinyl)-methyl] 3,4dihydro 2H [1,3]oxazino[3,2 a]indole10-carboxamide hydrochloride, SB 207266; (endo 3,9 dimethyl 3,9 diazabicyclo[3,3,1]non 7 yl 1H indazole 3 carboxamide dihydrochloride), N 3389; [(+) 8,9 dihydro 10 methyl 7 [(5 methyl 4 imidazolyl)methyl]pyrido [1,2 a] indole 6(7H) one hydrochloride], FK1052; 2 (cis 3,5 dimethylpiperidino)ethyl 4 amino 5 chloro 2 methoxybenzoate, ML10375; [3 (piperidine 1 yl)propyl 4 amino 5 chloro 2 methoxybenzoate hydrochloride], RS 23597 190; (1-[2-[(methylsulphonyl)amino]-ethyl]-4-piperidinyl-methyl-5-fluoro-2-methoxy-1H-indole-3-carboxylate), GR125487; R50595 (FR76530); RS100302; 1-(1-methylethyl)-N-[2-[4-[tricyclo[3.3.1.1 (3,7)]dec-1-ylcarbonyl)amino]-1-piperidinyl]ethyl-1H-indazole-3-carboxamide, LY353433; A-85380; SB205800; SB 207058; SB 207226; SC-53606 and SC 56184.