AU2007237240A1 - Use of calmodulin kinase II inhibitors to treat myocardial dysfunction in structural heart disease - Google Patents

Description

AUSTRALIA

Patents Act 1990 COMPLETE SPECIFICATION Standard Patent Applicant: VANDERBILT UNIVERSITY Invention Title: USE OF CALMODULIN KINASE II INHIBITORS TO TREAT MYOCARDIAL DYSFUNCTION IN STRUCTURAL HEART DISEASE The following statement is a full description of this invention, including the best method for performing it known to me/us: N: \Melbourne\Cases\Patent\52000-52999\P52624 .AU. 1\Specis\P52624.AU.1 Speci.doc 28/11/07 SUSE OF CALMODULIN KINASE II INHIBITORS TO TREAT MYOCARDIAL DYSFUNCTION IN STRUCTURAL HEART DISEASE 0 Z This application claims priority to U.S. provisional applications Serial No.

00 60/326, 576 filed October 1,2001, and Serial No. 60/328, 010, filed October 8, 2001.

The 60/326, 576 and the 60/328,010 provisional patent applications are herein incorporated by this reference in their entirety.

BACKGROUND

Field of the Invention SThe invention relates to the inhibition of Calmodulin kinase II (CaMKII).

(C More specifically, the CaMKII inhibition can treat or prevent structural heart disease, for example contractile dysfunction following a myocardial infarction, or dilated cardiomyopathy.

Background Art All references, including any patents or patent applications, cited in this specification are hereby incorporated by reference. No admission is made that any reference constitutes prior art. The discussion of the references states what their authors assert, and the applicants reserve the right to challenge the accuracy and pertinency of the cited documents. It will be clearly understood that, although a number of prior art publications are referred to herein, this reference does not constitute an admission that any of these documents forms part of the common general knowledge in the art, in Australia or in any other country.

Myocardial infarction is a major cause of significant disability and death in the United States and in many other countries around the world, and accounts for approximately 2/3 of all heart failure.

7 Several disease-initiating events myocardial infarction, untreated hypertension, congenital mutations of contractile proteins) can result in a common heart disease phenotype that consists of dilation of the cardiac chambers, resulting in reduction in contractile function a decrease in the fraction of total blood ejected from each chamber during systole) that leads to the clinical syndrome of heart failure.

7 Dilated cardiomyopathy includes two distinct disease entities. Dilated cardiomyopathy, as used herein, includes ischemic cardiomyopathy which is a disease entity 0 hypertrophy of surviving, non-infarcted myocardium is insufficient.

7 "Dilated 0 cardiomyopathy" can also include increased myocardial mass and reduced contractile C 5 function due to a genetic abnormality of myocardial proteins in the absence of ¢C myocardial infarction. A subject with dilated cardiomyopathy is a subject who has decreased cardiac contractility due to dilation of the ventricles. Thus, a subject with Sdilated cardiomyopathy and contractile dysfunction has different and more severe dysfunction than a subject in whom hypertrophy of surviving non-infarcted myocardium has compensated for infarcted myocardium. Further, a subject with dilated cardiomyopathy and contractile dysfunction has disease that is distinct from other cardiac conditions including abnormal relaxation diastolic dysfunction and cardiac arrhythmia.

Available therapies for heart failure are insufficient, and new methods of treatment are needed. The heart responds to infarction by hypertrophy of surviving cardiac muscle in an attempt to maintain normal contraction. However, when the hypertrophy is insufficient to compensate, dilated cardiomyopathy and reduced contractile function result, leading to heart failure and death.

1 9 Despite important advances in medical therapies for preventing cardiac dysfunction and heart failure after myocardial infarction, 15 these problems remain a significant unsolved public health problem.

No pharmacological therapy for dilated cardiomyopathy is curative or satisfactory, and many patients die or, in selected cases, undergo heart transplantation.

Presently available pharmacological therapies for reducing cardiac dysfunction and reducing mortality in patients with heart failure fall into three main categories: angiotensin-converting enzyme (ACE) inhibitors, beta adrenergic receptor (3AR) antagonists, and aldosterone antagonists. Despite reducing mortality, patients treated with these medicines remain at significantly increased risk for death compared to agematched control patients without heart failure. ACE inhibitors,"PAR antagonists 4 and

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z (at least one type of) aldosterone receptor antagonistl2can significantly reduce the 00 incidence and extent of cardiac dysfunction and heart failure after myocardial infarction. Other available pharmacological therapies include nitroglycerin, diuretics, positive inotropic agents (cardiac stimulants), and brain natriuretic peptide (BNP).

C 5 These latter agents can provide symptomatic relief, but are not associated with reduced n mortality in heart failure patients.

ACE inhibitors are associated with cough in 10% of patients and can result in Srenal failure in the setting of bilateral renal artery stenosis or other severe kidney disease.

7 AR antagonists are associated with impotence and depression, and are contraindicated in patients with asthma; furthermore, patients may develop worsened heart failure, hypotension, bradycardia, heart block, and fatigue with initiation of PAR antagonists 7 Aldosterone receptor antagonism causes significant hyperkalemia and painful gynecomastia in 10% of male patients.

7 2 Agents without a demonstrated mortality benefit are also associated with problems; most notable is the consistent finding that many cardiac stimulants improve symptoms, but actually increase mortality, 7 likely by triggering lethal cardiac arrhythmias. In contrast, CaMKII inhibition is now known to reduce cardiac arrhythmias in animal models, 20 2 1 and so represents a novel approach to enhancing cardiac function without increasing arrhythmias. Presently available pharmacological therapies are ineffective and are limited by significant unwanted side effects, and so development of new therapies with improved efficacy and less severe side effects is an important public health goal.

Calmodulin kinase IT is an enzyme that is present in heart and is activated when Ca- increases inside the heart cells, and binds to the Ca 2 binding protein calmodulin.

3 CaMKIII activity can increase in patients with severe cardiomyopathy, but CaMICI has never been linked to dilated cardiomyopathy or deterioration of contraction in heart failure.

The present invention provides methods of improving (increasing) contractile function of the myocardium to treat dilated cardiomyopathy and heart failure by inhibiting CaMKII. The present invention further provides mouse models of cardiactargeted CaMIKII inhibition by transgenic over expression of a selective CaMKII inhibitory peptide, AC3-I. Thus, the present AC3-I transgenic mouse is an important new tool to test for the effects of chronic CaMKII inhibition in cardiac disease.

SUMMARY OF THE INVENTION The present invention provides a method of treating or preventing myocardial dysfunction that follows myocardial infarction in a subject, comprising administering to the subject an effective amount of an inhibitor of Calmodulin Kinase II (CaMKII), whereby the administration of the inhibitor improves myocardial contraction after a myocardial infarction in the subject.

The present invention provides a method of treating or preventing myocardial dysfunction that occurs in dilated cardiomyopathy or other structural heart disease end-stage valve disease) in a subject diagnosed with dilated cardiomyopathy or other structural heart disease, comprising administering to the subject an effective amount of an inhibitor of CaMKII, whereby the administration of the inhibitor treats or prevents dilated cardiomyopathy or other structural heart disease in the subject.

The present invention provides a method of treating or preventing myocardial dysfunction that occurs in dilated cardiomyopathy in a subject diagnosed with dilated cardiomyopathy, comprising administering to the subject an effective amount of an inhibitor of CaMKII, whereby the administration of the inhibitor treats or prevents dilated cardiomyopathy or other structural heart disease in the subject.

The present invention provides a method of increasing myocardial contractility in a subject diagnosed with dilated cardiomyopathy, comprising administering to the subject an effective amount of an inhibitor of CaMlKII, whereby the administration of the inhibitor increases myocardial contractility in the subject.

Further provided by the present invention is a method of increasing myocardial contractility in a subject diagnosed with cardiac dysfunction and/or decreased 0 Z contractility following a myocardial infarction, comprising administering to the subject S00 an effective amount of an inhibitor of CaMKII, whereby the administration of the inhibitor increases myocardial contractility in the subject.

O Further provided by the present invention is a method of increasing myocardial C 5 contractility in a subject diagnosed with decreased myocardial contractility following a myocardial infarction, comprising administering to the subject an effective amount of an inhibitor of CaMKII, whereby the administration of the inhibitor increases Smyocardial contractility in the subject.

The present invention provides a method of identifying a compound that can treat structural heart disease, comprising: a) measuring cardiac contractility in an animal with structural heart disease; b) administering the compound to the animal of step c) measuring cardiac contractility in the animal of step and detecting an increase in cardiac contractility in the animal of step compared to cardiac contractility in the animal of step whereby the detection of an increase in cardiac contractility identifies a compound that can treat structural heart disease.

The present invention provides a method of treating structural heart disease in a subject, comprising administering to the subject an effective amount of a compound identified by the method of the present invention.

The present invention provides a transgenic animal,which expresses a nucleic acid encoding an inhibitor of CaMKII.

The present invention also provides a transgenic animal which expresses a nucleic acid encoding a peptide comprising the peptide of SEQ ID NO:8, which is referred to as AC3-C.

The present invention further provides a dual transgenic animal.which expresses a nucleic acid encoding an inhibitor of CaMKII and a nucleic acid expressing calcineurin.

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00 0, BRIEF DESCRIPTION OF THE DRAWINGS Figure. 1. A diagram of the domain structures of CaMK I, II, and IV, and the CaMKII inhibitory and control peptides expressed in the AC3-I and AC3-C transgenic r mice engineered for the present studies. CaMKII and IV both have a regulatory domain (black rectangle) that consists of CaM-binding and autoinhibitory (AI) regions. The C CaM binding region of CaMKII (296-309, numbered according to CaMII and marked by italics) is very similar in CaMKIV (identical amino acids are underlined), and inhibitory peptides directed against the CaM-binding sequence in CaMIGI similarly inhibit activation of CaMKIV 1 7 AC3-I is modeled on the AI region of CaMKII that is centered around Thr 286 (marked with an arrow), and is dissimilar in CaMKII and CaMKIV. Neither the CaM-binding or AI regions of CaMKI are homologous to CaMKII or IV, but, in contrast to the AI region, inhibitory peptides directed against the CaM-binding region of CaMKII or IV may nevertheless inhibit CaMKI because CaMbinding domains commonly share an a helical structure, but often lack primary sequence homology.

13 Figures 2 A-E. AC3-I mice have normal cardiac size and systolic function. A and B. Echocardiographic left ventricular dimensions are not significantly different between AC3-I mice and wild-type (WT) littermate controls in diastole or systole C and D. Interventricular septal thickness is not different between AC3-I mice and WT littermate controls in diastole or systole E. Left ventricular fractional shortening is not different between AC3-I and WT littermate control mice at baseline.

Open bars are WT and black bars are AC3-I transgenic (TG) in all panels. The number of mice studied in each line number (indicated in panel E) is the same in all panels.

Figures 3 A-B. AC3-I mice have significantly reduced cardiac CaMIII activity and significantly better left ventricular fractional shortening after myocardial infarction surgery than wild type (WT) littermate controls. CaMKII activity measurements are from whole heart homogenates.

Figure 4. Transgene expression in AC3-I and AC3-C mice by GFP Western 00 blots. Line numbers are indicated in parenthesis to indicate identity in Western blots and corresponding quantitative phosphorimaging (data normalized to AC3-I line 0The genetic identity of all transgenic mice was confirmed by Southern analysis, but N 5 AC3-I line 3 did not express the transgene.

l^- Ce Figures 5 A-C. AC3-C transgenic mice (from line 1) develop dilated cardiomyopathy. The left ventricular internal diameter (LVID) is significantly greater 0in AC3-C than AC3-I mice *P<0.01, from line 4) in diastole, indicating a dilated phenotype. The LVID shortens significantly less in AC3-C than in AC3-I mice during systole, indicating reduced ventricular function. In contrast to LVID, the interventricular septum (IVS) and the left ventricular posterior wall (LVPW) are not significantly different between AC3-I and AC3-C mice in diastole or systole. C. Left ventricular fractional shortening is significantly depressed in AC3-C compared to AC3-I mice (P<0.001). D. The heart rates are not different between AC3-I and AC3-C mice.

Figures 6 A-B. Total CaMKII activity is significantly reduced in ventricular homogenates from AC3-I compared to AC3-C mice and wild-type (WT) littermates.

A. Total CaMKII activity. B. Ca 2 '-independent fraction of CaMKII activity.

Figures 7 A-D. CaMKII inhibition improves contractile function after myocardial infarction surgery. Echocardiographic measurements in unanesthetized mice 3 weeks after myocardial infarction surgery reveal significantly preserved left ventricular function in mice with CaVMII inhibition. A. Left ventricular (LV) fractional shortening is significantly greater in mice treated daily with the CaMKII inhibitory agent KN-93 (at 1 and 10 gmol/Kg body weight) and in AC3-I mice with transgenically targeted CaMKII inhibition than in wild type littermate controls (WT) or in WT mice treated daily with the inactive KN-93 congener KN-92 (30 Ltmol/Kg body weight). P<0.001 by ANOVA and asterisks indicate a significant difference compared to WT using a Bonferroni -corrected t test. B. LV internal diameter (LVID) during diastole is a marker of LV chamber dilation. No significant differences in LVID during 0 Z diastole were present between groups. C. LV posterior wall (LVPW) wall thickness in 00 diastole is a measure of LV hypertrophy of the non-infarcted wall. No significant differences in LVPW in diastole were present between groups. D. Heart rate was significantly slower in AC3-I mice with transgenically targeted CaMKII inhibition compared to all other groups.

SFigure 8. CaMKII inhibition reduces left ventricular dilation and improves left r'ventricular contractile function in dilated cardiomyopathy. Dual transgenic (AC3- I+/CAN+) have reduced left ventricular (LV) dilation and improved LV fractional shortening compared to CAN+ transgenic mice.

10 Echocardiographic measurements in unanesthetized calcineurin (CAN+) transgenic and interbred dual transgenic AC3- I+/CAN+ mice show LV internal diameter (LVID) is significantly reduced in diastole and the interventricular septum (IVS) and the LV posterior wall (LVPW) are increased in diastole in AC3-I+/CAN compared to CAN+ mice, indicating partial rescue of the dilated cardiomyopathy phenotype by transgenically targeted CaMKII inhibition.

Measurement parameters are the same for the top 4 panels: left ventricular internal diameter (LVID), interventricular septum (IVS), and left ventricular posterior wall (LVPW). Left ventricular systolic function is significantly increased in the dual transgenic AC3-I+/CAN+ mice compared to the CAN+ mice, indicating improved contractile function by transgenically targeted cardiac CaMKII inhibition. In contrast, there are no significant differences between heart rates in the AC3-I+/CAN+ and CAN+ transgenic animals. All mice were between 4-8 weeks of age.

Figures 9 A-B. Strategy for interbreeding AC3-I or AC3-C and Calcineurin (CAN) transgenic mice. A. Boxes indicate breeding pairs. The primary comparison will be between CAN positive mice, but alternative comparisons (that provide data shown in Figure 8) are also shown. B. PCR results reveal that interbreeding between AC3-I and CAN mice is successful and that dual transgenic mice can be identified with standard PCR methods.

N: \Melboure\Cases\Patent\52000-52999\P52624.AU.1\Specis\P52624.AU.1 Speci.doc 28/11/07 DETAILED DESCRIPTION OF THE INVENTION 0 It must be noted that, as used in the specification and the appended claims, the Ssingular forms and "the" include plural referents unless the context clearly 00 dictates otherwise. Thus, for example, reference to "an inhibitor" includes multiple copies of the inhibitor and can also include more than one particular species of inhibitor.

SIn the claims which follow and in the description of the invention, except Swhere the context requires otherwise due to express language or necessary implication, C 10 the word "comprise" or variations such as "comprises" or "comprising" is used in an 0inclusive sense, i.e. to specify the presence of the stated features but not to preclude the NC presence or addition of further features in various embodiments of the invention.

The present invention provides a method of treating or preventing myocardial contractile dysfunction after a myocardial infarction in a subject diagnosed with myocardial contractile dysfunction after a myocardial infarction, comprising administering to the subject an effective amount of an inhibitor of Calmodulin Kinase II (CaMKII), whereby the administration of the inhibitor treats or prevents myocardial contractile dysfunction after myocardial infarction in the subject. In general, an "effective amount" of an inhibitor is that amount needed to achieve the desired result or results. By "myocardial infarction" is meant an ischemic injury to the heart in which part of the myocardium (heart muscle) has undergone necrosis or apoptosis, i.e., programmed cell death. An "ischemic injury" means the damage or potential damage to an organ or tissue that results from the interruption of blood flow to the organ or tissue, an ischemic event. As used throughout, by a "subject" is meant an individual. Thus, the "subject" can include domesticated animals, such as cats, dogs, etc., livestock cattle, horses, pigs, sheep, goats, etc.), laboratory animals mouse, rabbit, rat, guinea pig, etc.) and birds. Preferably, the subject is a mammal such as a primate, and more preferably, a human.

The subject can be a patient diagnosed as having a myocardial infarction. The subject can be a patient diagnosed as having post-infarction cardiac dysfunction. The subject can be a patient who has been diagnosed as having had a myocardial infarction who is, thus, at increased risk of developing post-infarction cardiac dysfunction.

Further, the subject can be a patient diagnosed as having dilated cardiomyopathy or symptoms of heart failure from any cause associated with a phenotype of cardiac 0 Z chamber dilation and reduced myocardial contractile function. The subject can be a 00 patient diagnosed as having reduced myocardial contractility. Methods of diagnosing myocardial infarction, post-infarction cardiac dysfunction, reduced myocardial Scontractility and dilated cardiomyopathy are well known in the art. Methods of distinguishing subjects having post-infarction contractile dysfunction or dilated cardiomyopathy from subjects having myocardial infarction or having myocardial hypertrophy are well known in the art. It is recognized that a subject diagnosed with myocardial infarction, or a subject diagnosed with cardiac arrhythmia, or a subject diagnosed with myocardial hypertrophy does not necessarily have dilated cardiomyopathy or reduced myocardial contractility.

An inhibitor of CaMKII can be any compound, composition or agent that inhibits the activity or expression the amount or the disease-causing effect) of CaMKII. The compound can be a peptide or non-peptide agent, including, for example, a nucleic acid that encodes a peptide inhibitor. Moreover, the agent can be an antisense nucleic acid that inhibits expression of CaMKII in the heart (see GenBank accession numbers L13407 for isoform 53 and 82 from Hoch et al., Circ Res 1999 in Figure 9 of this application) 5 By "inhibit" is meant to restrict, hold back or reduce.

Thus, an inhibitor is an agent that can, for example, reduce an activity of an enzyme or the amount of expression of an enzyme, or both. The inhibition can be reversible or irreversible. CaMKII activity in a subject or the amount of CaMKII in a subject can be readily determined based on detection or measurement of a functional response, for example as determined by echocardiography or by other clinical parameters. Specific methods of measuring CaMKII activity in a non-human animal model are provided herein. Thus, it is routine to identify compounds that inhibit CaMKII.

An example of an inhibitor of CaMKI is a peptide comprising the peptide of SEQ ID NO:2, which is also referred to herein as AC3-I.. The inhibitor of the invention can consist of the peptide of SEQ .D NO:2.

Another example of an inhibitor of CaMKII is a peptide comprising the peptide of SEQ ED NO:4, which is CaM-KIHN. The inhibitor can be the full-length CaM-KIIN 0

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Z (SEQ ID NO:4) and/or a fragment of the full-length peptide; the fragment is called 00 CaM-KIINtide (SEQ ID NO:6). CaMKIN and CaM-KIINtide are described in Chang et al. PNAS (USA) 1998 95:10890-10895, which is herein incorporated by reference in 0its entirety.

CN 5 Because each of these is shown to inhibit CaMKII, it is expected that other peptides and polypeptides that contain it but include non-essential amino acids will have similar activity. A non-essential amino acid is an amino acid that will not affect the function of the peptide or the way the peptide accomplishes that function its secondary structure or the ultimate result of the activity of the peptide). Examples of non-essential amino acids in the present invention include, but are not limited to, the amino acids comprising GFP, a peptide label that tags and identifies proteins or peptides for purification There are numerous other inhibitors of CaMKII that are contemplated by the present invention, one of which is KN-93. KN-93, a non-peptide inhibitor of CaMKII, is described in WO 98/33491, which is herein incorporated by reference in its entirety for its teaching with regard to KN-93 and inhibitors of CaMKII.

The present invention further provides a method of treating or preventing cardiac dysfunction following myocardial infarction in a subject, comprising administering to the subject an effective amount of an inhibitor of CaMKII, whereby the administration of the inhibitor treats or prevents the cardiac dysfunction in the subject. By "cardiac dysfunction" is meant reduced contractile function of the blood pumping chambers that results in the clinical condition of heart failure. Methods of diagnosing cardiac dysfunction following a myocardial infarction in a subject are well known in the art.

In the method of treating or preventing cardiac dysfunction following a myocardial infarction in a subject, the inhibitor of CaMKII can be a peptide, for example, a peptide comprising the peptide of SEQ ID NO:2, or a peptide consisting of the peptide of SEQ ID NO:2. The inhibitor of CaMKII can be a peptide comprising the peptide of SEQ ID NO:4 or a peptide consisting of the peptide of SEQ ID NO:4.

0 Z Further, the inhibitor can be a peptide comprising the peptide SEQ ID NO:6 or a 00 0, peptide consisting of the peptide of SEQ ID NO:6. The inhibitor can be a non-peptide inhibitor, for example, an inhibitor comprising the active region of KN-93 or it can be O KN-93.

The present invention also provides a method of treating or preventing dilated cardiomyopathy or any heart disease with the phenotypes of cardiac chamber dilation from any cause in a subject, comprising administering to the subject an effective amount of an inhibitor of CaMKII, whereby the administration of the inhibitor treats dilated cardiomyopathy or reduces cardiac chamber dilation in the subject. Methods of diagnosing dilated cardiomyopathy in a subject are well known in the art.

In the method of treating or preventing dilated cardiomyopathy, the inhibitor of CaMKII can be a peptide, for example, a peptide comprising the peptide of SEQ ID NO:2, or a peptide consisting of the peptide of SEQ ID NO:2. The inhibitor of CaMKII can be a peptide comprising the peptide of SEQ ID NO:4 or a peptide consisting of the peptide of SEQ ID NO:4. Further, the inhibitor can be a peptide comprising the peptide SEQ ID NO:6 or a peptide consisting of the peptide of SEQ ID NO:6. The inhibitor can be a non-peptide inhibitor, for example, an inhibitor comprising the active region of KN-93 or it can be KN-93.

The present invention provides a method of increasing myocardial contractility in a subject diagnosed with dilated cardiomyopathy or any heart disease with the phenotypes of cardiac chamber dilation or reduced contractile function from any cause, comprising administering to the subject an effective amount of an inhibitor of CaMKII, whereby the administration of the inhibitor improves myocardial contractility in the subject. Techniques for measuring cardiac contractility, for example echocardiography, radionucleotide angiography, and magnetic resonance imaging are well known in the art. As used herein, "myocardial contractility" is a measure of the contraction of the heart muscle, more specifically, of the left ventricle. As shown in Figure 7, AC3-I and KN-93 increase myocardial contractility (a positive inotropic effect) without affecting cardiac hypertrophy.

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Z Further, the present invention provides a method of increasing myocardial 00 contractility in a subject diagnosed with myocardial infarction, comprising administering to the subject an effective amount of an inhibitor of CaMKII, whereby O the administration of the inhibitor improves myocardial contractility in the subject.

N 5 The present invention also provides a method of increasing myocardial e contractility in a subject diagnosed with cardiac dysfunction following a myocardial infarction, comprising administering to the subject an effective amount of an inhibitor O of CaMKII, whereby the administration of the inhibitor improves myocardial contractility in the subject.

In the method of increasing myocardial contractility, the inhibitor of CaMKII can be a peptide, for example, a peptide comprising the peptide of SEQ ID NO:2, or a peptide consisting of the peptide of SEQ ID NO:2. The inhibitor of CaMKII'can be a peptide comprising the peptide of SEQ ID NO:4 or a peptide consisting of the peptide of SEQ ID NO:4. Further, the inhibitor can be a peptide comprising the peptide SEQ ID NO:6 or a peptide consisting of the peptide of SEQ ID NO:6. The inhibitor can be a non-peptide inhibitor, for example, an inhibitor comprising the active region of KN-93 or it can be KN-93.

An inhibitor of CaMKII can be used to increase contractility of the myocardium without affecting myocardial hypertrophy, thereby treating a subject diagnosed with myocardial infarction, cardiac dysfunction following a myocardial infarction and/or dilated cardiomyopathy.

The present invention provides a method of identifying a compound that can treat structural heart disease, comprising: a) measuring cardiac contractility in an animal with structural heart disease; b) administering the compound to the animal of step c) measuring cardiac contractility in the animal of step and d) detecting an increase in cardiac contractility in the animal of step compared to cardiac contractility in the animal of step whereby the detection of an increase in cardiac contractility identifies a compound that can treat structural heart disease. In the method of this invention, the animal with structural heart disease can be a transgenic animal Z that expresses AC3-C. Methods of measuring cardiac contractility are well known in 00 0'1 the art and include, but are not limited to, echocardiography. Such methods include radionucleotide angiography, magnetic resonance imaging, and left ventricular angiography.

N. 5 The present invention provides a method of identifying a compound that can treat structural heart disease, comprising: a) measuring brain natriuretic peptide in an animal with structural heart disease; b) administering the compound to the animal of CN step c) measuring brain natriuretic peptide in the animal of step and d) detecting an increase in brain natriuretic peptide in the animal of step compared to brain natriuretic peptide in the animal of step whereby the detection of an increase in brain natriuretic peptide identifies a compound that can treat structural heart disease.

In the method of this invention, the animal with structural heart disease can be a transgenic animal that expresses AC3-C.

Heart failure is a clinical syndrome that includes reduced exercise tolerance due to reduction in cardiac contraction and tissue oxygenation, 7 so exercise testing by treadmill or bicycle ergonometry, reduced tissue oxygen uptake, or increased plasma brain natriuretic peptide levels are all markers of heart failure severity. Values denoting extreme and moderate impairment of myocardial contraction, exercise capacity, maximum oxygen consumption, and circulating brain natriuretic peptide levels are well described and known to one skilled in the art of treating heart failure. Examples of structural heart disease include, but are not limited to, myocardial infarction, cardiac dysfunction following myocardial infarction, reduced myocardial contractility and dilated cardiomyopathy.

The present invention provides a method of treating myocardial infarction, cardiac dysfunction following myocardial infarction and/or dilated cardiomyopathy in a subject, comprising administering to the subject an effective amount of the compound identified by the above-described method, whereby the administration of the compound to the subject treats cardiac dysfunction following myocardial infarction and/or dilated 0 0 Z cardiomyopathy or patients with heart failure and dilated cardiac chambers and reduced 00 left ventricular contractility.

The present invention provides a transgenic animal that expresses a nucleic acid 0 encoding an inhibitor of CaMKII. By "transgenic animal" is meant an animal in which C 5 all the cells of its body comprise an exogenous nucleic acid. In one example of a eC transgenic animal of the invention, the transgene is specifically expressed in heart muscle cells, driven by a heart cell specific promoter. This mouse was engineered with 0 a cardiac-specific a myosin heavy chain promoter (GenBank accession U71441).

Methods of making transgenic animals are well known in the art, and specifically exemplified herein.

In the transgenic animal of the present invention, the inhibitor of CaMKII that is expressed can be a peptide comprising the peptide of SEQ ID NO:2. Moreover, the transgenic animal of the invention can express the peptide consisting of the peptide of SEQ ID NO:2. Recent reports have found at least 4 varieties of the CaMKII 8 isoform in heart, 5 and AC3-I (SEQ ID NO:2) inhibits all CaMKII isoforms, due to conservation of the targeted regulatory domain.

3 The AC3-I targeted domain in CaMKII is dissimilar to analogous functional domains in other CaMK types CaMKI and CaMKIV, Figure and is virtually devoid of activity against protein kinases A and C.

3 In the transgenic animal of the invention, the inhibitor of CaMKII that is expressed can be a peptide comprising the peptide of SEQ ID NO:4. Moreover, the transgenic animal of the invention can express the peptide consisting of the peptide of SEQ ID NO:4.

The invention further provides a transgenic animal which expresses in heart muscle cells a nucleic acid encoding a peptide comprising the peptide of SEQ ID NO:8, which is also referred to as AC3-C. As shown in figures 4 and 5, AC3-I and AC3-C mice have similar expression of transgene, but AC3-C mice exhibit cardiomyopathy, whereas AC3-I mice with CaMKII inhibition are normal. As shown in figure 6, the AC3-C mice have high total CaMKII activity as is seen in human patients with cardiomyopathy. Thus, this transgenic animal can be used in the present method of identifying a compound that can treat structural heart disease. Because AC3-C is 00 believed to be inactive, these results may be explained by an effect of the green

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fluorescent protein (GFP) moiety of the AC3-C-GFP transgene.

6 This mouse is made following the basic protocol for making the AC3-I transgenic mouse.

The present invention also provides a dual transgenic animal (AC3-I+/CAN+) which expresses in heart muscle cells a nucleic acid encoding AC3-I and a nucleic acid encoding calcineurin. The calcineurin (CAN+) transgenic mouse is a well accepted S model of severe dilated cardiomyopathy.' 0 CAN antagonists are known to 'rescue' the cardiomyopathy phenotype in a variety of mouse models, 1 6 but CaMKI inhibition has never been contemplated to improve cardiac function or structure in these or any other models of cardiomyopathy. As exemplified in Figure 8, the dual transgenic animal, which expresses an inhibitor of CaMKII in addition to CAN, improves left ventricular function and shows reduced left ventricular dilation and hypertrophy when compared to CAN+ animals. Thus, inhibition of CaMKII in this animal treats dilated cardiomyopathy.

In the methods of the invention, an inhibitor of CaMKII can be administered by known means. In a specific example, the peptide inhibitors are made cell membrane permeant. By cell "membrane permeant" is meant able to pass through the openings or interstices in a membrane 1 6 This method uses a peptide sequence that is added to the inhibitory peptide, but myristoylation is another approach for making a peptide cell membrane permeant.

The compositions of the present invention can also be administered in vivo in a pharmaceutically acceptable carrier. By "pharmaceutically acceptable" is meant a material that is not biologically or otherwise undesirable, the material may be administered to a subject, along with the composition, without causing any undesirable biological effects or interacting in a deleterious manner with any of the other components of the pharmaceutical composition in which it is contained. The carrier would naturally be selected to minimize any degradation of the active ingredient and to minimize any adverse side effects in the subject, as would be well known to one of skill in the art.

The compositions may be administered orally, parenterally intravenously, intramuscularly, intrathecally, intraarterially and by intraperitoneal injection), transdermally, extracorporeally, topically or the like, although topical intranasal administration or administration by inhalant is typically preferred. As used herein, "topical intranasal administration" means delivery of the compositions into the nose and nasal passages through one or both of the nares and can comprise delivery by a spraying mechanism or droplet mechanism, or through aerosolization of the therapeutic agent. Delivery can also be directly to any part of the lower respiratory tract trachea, bronchi and lungs) via intubation. The exact amount of the compositions required will vary from subject to subject, depending on the species, age, weight and general condition of the subject, the severity of the condition being treated, the particular composition used, its mode of administration and the like. Thus, it is not possible to specify an exact amount for every composition. However, an appropriate amount can be determined by one of ordinary skill in the art using only routine experimentation given the teachings herein.

Parenteral administration of the composition, if used, is generally characterized by injection. Injectables can be prepared in conventional forms, either as liquid solutions or suspensions, solid forms suitable for solution of suspension in liquid prior to injection, or as emulsions. A more recently revised approach for parenteral administration involves use of a slow release or sustained release system such that a constant dosage is maintained. See, U.S. Patent No. 3.610,795, which is incorporated by reference herein.

The materials may be in solution, suspension (for example, incorporated into microparticles, liposomes, or cells). These may be targeted to a particular cell type via antibodies, receptors, or receptor ligands. The following references are examples of the use of this technology to target specific proteins to tumor tissue (Senter, et al., Bioconjugate Chem., 2:447-451, (1991); Bagshawe, Br. J. Cancer, 60:275-281, 0 Z (1989); Bagshawe, et al., Br. J. Cancer, 58:700-703, (1988); Senter, et al., Bioconiugate oO 00 Chem., 4:3-9, (1993); Battelli, et al., Cancer Immunol. Immunother., 35:421-425, (1992); Pietersz and McKenzie, Immunolog. Reviews, 129:57-80, (1992); and Roffler, et al., Biochem. Pharmacol, 42:2062-2065, (1991)). Vehicles such as "stealth" and N 5 other antibody conjugated liposomes (including lipid mediated drug targeting to colonic carcinoma), receptor mediated targeting of DNA through cell specific ligands, lymphocyte directed tumor targeting, and highly specific therapeutic retroviral targeting (S of murine glioma cells in vivo. The following references are examples of the use of this technology to target specific proteins to tumor tissue (Hughes et al., Cancer Research, 49:6214-6220, (1989); and Litzinger and Huang, Biochimica et Biophysica Acta, 1104:179-187, (1992)). In general, receptors are involved in pathways of endocytosis, either constitutive or ligand induced. These receptors cluster in clathrin-coated pits, enter the cell via clathrin-coated vesicles, pass through an acidified endosome in which the receptors are sorted, and then either recycle to the cell surface, become stored intracellularly, or are degraded in lysosomes. The internalization pathways serve a variety of functions, such as nutrient uptake, removal of activated proteins, clearance of macromolecules, opportunistic entry of viruses and toxins, dissociation and degradation of ligand, and receptor-level regulation. Many receptors follow more than one intracellular pathway, depending on the cell type, receptor concentration, type of ligand, ligand valency, and ligand concentration. The molecular and cellular mechanisms of receptor-mediated endocytosis have been reviewed (Brown and Greene, DNA and Cell Biology 10:6, 399-409 (1991)).

The compositions of the present invention can include a nucleic acid encoding an inhibitor or can include a CaMKII antisense nucleic acid. The disclosed compositions can be delivered to the target cells in a variety of ways. For example, the compositions can be delivered through electroporation, or through lipofection, or through calcium phosphate precipitation. The delivery mechanism chosen will depend in part on the type of cell targeted and whether the delivery is occurring for example in vivo or in vitro.

0 Z Thus, the compositions can comprise, in addition to the disclosed compositions 00 or vectors for example, lipids such as liposomes, such as cationic liposomes DOTMA, DOPE, DC-cholesterol) or anionic liposomes. Liposomes can further Scomprise proteins to facilitate targeting a particular cell, if desired. Administration of a N 5 composition comprising a compound and a cationic liposome can be administered to c the blood afferent to a target organ or inhaled into the respiratory tract to target cells of Sthe respiratory tract. Regarding liposomes, see, Brigham et al. Am. J. Resp. Cell.

Mol. Biol. 1:95-100 (1989); Feigner et al. Proc. Natl. Acad. Sci USA 84:7413-7417 (1987); U.S. Pat. No.4,897,355. Furthermore, the compound can be administered as a component of a microcapsule that can be targeted to specific cell types, such as macrophages, or where the diffusion of the compound or delivery of the compound from the microcapsule is designed for a specific rate or dosage.

In the methods described above which include the administration and uptake of exogenous DNA into the cells of a subject gene transduction or transfection), delivery of the compositions to cells can be via a variety of mechanisms. As one example, delivery can be via a liposome, using commercially available liposome preparations such as LPOFECTIOFECT LOFECTAMINE (GIBCO-BRL, Inc., Gaithersburg, MD), SUPERFECT (Qiagen, Inc. Hilden, Germany) and TRANSFECTAM (Promega Biotec, Inc., Madison, WI), as well as other liposomes developed according to procedures standard in the art. In addition, the nucleic acid or vector of this invention can be delivered in vivo by electroporation, the technology for which is available from Genetronics, Inc. (San Diego, CA) as well as by means of a SONOPORATION machine (ImaRx Pharmaceutical Corp., Tucson, AZ).

Nucleic acids that are delivered to cells which are to be integrated into the host cell genome, typically contain integration sequences. These sequences are often viral related sequences, particularly when viral based systems are used. These viral integration systems can also be incorporated into nucleic acids which are to be delivered using a non-nucleic acid based system of delivery, such as a liposome, so that the nucleic acid contained in the delivery system can be come integrated into the host 0 Z genome. As used herein, "nucleic acid" includes single- or double-stranded molecules Swhich may be DNA, comprised of the nucleotide bases A, T, C, G or RNA, comprised of the bases A, U (substitutes for C and G. The nucleic acid may represent a coding strand or its complement. Nucleic acids may be identical in sequence to the portion of the sequence which is naturally occurring or may include alternative codons which encode the same amino acid as that which is found in the naturally occurring sequence.

Furthermore, nucleic acids can include codons which represent conservative C substitutions of amino acids as are well known in the art.

Other general techniques for integration into the host genome include, for example, systems designed to promote homologous recombination with the host genome. These systems typically rely on sequence flanking the nucleic acid to be expressed that has enough homology with a target sequence within the host cell genome that recombination between the vector nucleic acid and the target nucleic acid takes place, causing the delivered nucleic acid to be integrated into the host genome.

Those of skill in the art know these systems and the methods necessary to promote homologous recombination.

As described above, the compositions can be administered in a pharmaceutically acceptable carrier and can be delivered to the cells of the subject in vivo and/or ex vivo by a variety of mechanisms well known in the art uptake of naked DNA, liposome fusion, intramuscular injection of DNA via a gene gun, endocytosis and the like). If ex vivo methods are employed, cells or tissues can be removed and maintained outside the body according to standard protocols well known in the art. The compositions can be introduced into the cells via any gene transfer mechanism, such as, for example, calcium phosphate mediated gene delivery, electroporation, microinjection or proteoliposomes. The transduced cells can then be infused in a pharmaceutically acceptable carrier) or homotopically transplanted back into the subject per standard methods for the cell or tissue type. Standard methods are known for transplantation or infusion of various cells into a subject.

1 0 Z The inhibitor can be administered in any dose that is effective to inhibit 0 0 CaMKII activity or amount. As noted above, detection of a reduction in CaMKII activity or amount is well within the skill of the practitioner. More specifically, the O inhibitor can be administered in a dose of from about 0.05 mg to about 5.0 mg per kilogram of body weight. The inhibitor can, alternatively, be administered in a dose of from about 0.3 mg to about 3.0 mg per kilogram of body weight.

The following examples are put forth so as to provide those of ordinary skill in Sthe art with a complete disclosure and description of how the compositions and/or methods claimed herein are made and evaluated, and are intended to be purely exemplary of the invention and are not intended to limit the scope of what the inventors regard as their invention. Efforts have been made to ensure accuracy with respect to numbers amounts, temperature, etc.), but some errors and deviations should be accounted for. The present invention is more particularly described in the following examples which are intended as illustrative only since numerous modifications and variations therein will be apparent to those skilled in the art.

EXAMPLES

AC3-I transgenic mice: The AC3-I mice were generated by synthesis of a minigene based on the peptide sequence for AC3-I (Figure A 'minigene' encoding AC3-I (KKALHRQEAVDCL), 2 a CaMKII inhibitory peptide was constructed with these complementary oligonucleotides: (SEQ ID NO:1)

GATCAAAAAAGCCCTTCACCGCCAGGAGGCAGTTGACTGCCTTGCTTT'TC

GGGAAGTGGCGGTCCTCCGTCAACTGACGGAACGCTAG,

and a minigene was similarly constructed for a related, inactive control peptide, AC3-C (KKALHAQERVDCL) using the following complementary oligonucleotides: (SEQ ID NO:7) 00 00

GATCAAAAAAGCCCTTCACGCACAGGAGCGCGTTGACTGCCTTGC

TTTTTCGGGAAGTGCGTGTCCTCGCGCAACTGACGGAACGCTA

G

0 The minigene was inserted in frame with the EGFP into the BspEI site of pEGFP-C1 (Clontech), which places the EGFP at the N-terminus of the peptide. The AC3-I minigene includes a Kozak consensus translational start site. It was then sequenced and expressed in HEK293 cells to show green fluorescence. Previous studies indicated that an AC3-I-GST-MTS fusion peptide retained full CaMKII inhibitory potency against a synthetic CaMKII substrate (AC3-I-GST-MTS IC 50 0.4 gM; AC3-I IC 5 o 0.5 suggesting that the AC3-I-GFP protein would also retain CaMKII inhibitory activity. The 800 bp AC3-I-GFP sequence was then amplified using PCR, purified and subcloned into the SalIl site of a pBluescript vector containing the a- MHC promoter vector (GenBank accession U71441) and the human growth hormone (HGH) poly A tail (developed by Dr. J. Robbins). The construct was verified by sequencing and expressed in a murine atrial tumor cell line (HL1), which also showed reen fluorescence. Murine embryonic stem cells were injected with the linearized DNA (2 ng/ml) in the Vanderbilt Transgenic Mouse core facility and implanted in B6D2 pseudo-pregnant females.

The AC3-I is linked to green fluorescent protein (GFP) to reveal homogenous expression throughout the heart when histologic sections are examined under a microscope. These AC3-I mice are viable and have normal basal cardiac size and function (Figure However, hearts from these mice have significantly reduced total cardiac CaiKII activity (Figure and these mice have significantly less impairment of cardiac function after experimental myocardial infarction compared to wild type littermate controls (Figure These findings indicate that CaMKII activity is a novel signal for cardiac dysfunction after myocardial infarction and are the basis for our claim to treat patients with myocardial infarction by a method of CaMKII inhibition.

0 O O 00 AC3-I+/CAN+ transgeneic mice: Dual transgenic mice were interbred using the strategy schematized in Figure 9. For genotyping of the first generation, tail biopsies Swere taken at 3 weeks of age and were incubated overnight at 55 0 C in N 5 protease K, 50mM Tris (pH 100mM EDTA, and 0.5%SDS. Genomic DNA was Cc precipitated with an equal volume of isopropanol after performing phenol/chloroform/isoamyl alcohol (25:24:1) extraction twice. DNA was dissolved overnight in 50tll of 1/10 TE (pH 8.0) with 2.5ltg RNAase A. 15 ltg of genomic DNA was completely digested with EcoRI and digested DNA was separated on a 0.8% agarose gel in Ix TAE. After electrophoresis, the gel was incubated in 0.25N HCL for neutralized in 0.5M NaOH-1.5M NaCI for 15min twice and equilibrated in Tris-1.5M NaCI for 15min twice. The gel was blotted overnight on MSI nylon transfer membrane (Micron separations Inc. Westborought, MA) and the filter was UVcrosslinked. GFP-AC3I or GFP-AC3C DNA fragments were labeled with 32 P by random oligonucleotide priming (Stratagene, La Jolla, CA) as a probe. Hybridization was carried out overnight at 42 0 C in the presence of 50% Formamide, 5xSSPE, Denhardt's solution, 0.1% SDS, and 100 tg/ml denatured, fragmented salmon sperm DNA. The filter was washed in 0.5xSSC-0.1% SDS for 30min at 65 0 C, followed by a wash in 0.1xSSC-0.1% SDS for 20min twice at 65 0 C. The filter was exposed to Kodak autoradiography film and developed afterwards.

Routine screening of transgenic mice, after the first generation, was done by PCR (see Figure Two primers served to amplify a 442-bp region of the human growth hormone (hGH) gene at 3' end. The sequences of the primers are 5'-Hgh (SEQ ID NO:9) GTCTATTCGGGAACCAAGCT-3') and 3'-Hgh (5'-(SEQ ID ACAGGCATCTACTGAGTGGACC-3'). 100 ng purified genomic DNA was mixed with 200pM of each primer and amplified according to the following protocol: 95 0 C for min, followed by 30 cycles consisting of 95 0 C for 45 seconds, 50 0 C for 45 seconds, 72 0 C for Imin and a final 7min elongation at 72 0 C. All samples were run on a agarose gel in the presence of 0.5ptg/ml ethidium bromide and stained DNA bands were visualized under UV light. New primer sets were developed for the interbred dual 00lO transgenic mice (Fig 9) and these allow differentiation of dual and single transgenic animals.

Ecliocardiography: Echocardiography is performed using a Hewlett Packard Sonos 5500 (fully dedicated to murine studies) and a specially developed 12 MHz probe.

Cardiac dimensions are obtained from 2-D-guided M mode images and are read off line by blinded, independent readers using short axis and a parasternal long-axis views with the leading edge method. Animals can be lightly sedated with pentobarbital mg/Kg, however, measurements without anesthesia, where the mice undergo a brief 'training' period to acclimate to the procedure, can be made. Approximately of mice can be trained to undergo echocardiographic studies without the cardiodepressant effects of anesthesia. Measurements are averaged over 3 consecutive beats from the LV posterior wall (LVPW), the interventricular septum (IVS), and the LV internal diameter (LVID). Fractional shortening (FS) is used to estimate systolic function and is computed according to the formula FS=(LVIDdiastole- LVIDsystole)/LVlDdiastole x 100.

Myocardial infarction surgery: Surgery is routinely performed at the Vanderbilt mouse physiology core laboratory and is essentially identical to other published reports S In brief, mice are anesthetized (pentobarbital 33 Ag/g and ketamine 33 pg/g, i.p.) and placed on a rodent respirator (tidal vol. 0.5ml, rate 120 breaths/min), the chest opened with a left parastemal thoracotomy, and the region of the mid-left anterior descending artery ligated with 8-0 suture. The chest is closed (running 5-0 suture), and the animal weaned from the respirator. Wild-type mice typically develop heart failure, as assessed by increased lung wet:dry weights. Sham operations omit the ligation step.

Approximately 75% of animals survive surgery with a successfully infarcted anterior wall.

O

z CaMKII activity assays: CaMKII activity was assayed in AC3-I mice and littermate S00 controls from whole heart (ventricular) homogenate with syntide 2-a synthetic substrate with -50 fold selectivity for CaMKII over CaMKIV, 9 using our previously published methods.' C1 SDilated cardiomyopathy: Compelling data are presented on prevention of dilated cardiomyopathy by CaMKII inhibition. A control transgenic mouse that expresses GFP linked to AC3-C (an inactive congener of AC3-I) was made. This mouse develops rather severe dilated cardiomyopathy that is absent in the AC3-I-GFP mouse, and has very high levels of CaMKII activity (Figure Throughout this application, various publications are referenced. The disclosures of these publications in their entireties are hereby incorporated by reference into this application in order to more fully describe the state of the art to which this invention pertains.

It will be apparent to those skilled in the art that various modifications and variations can be made in the present invention without departing from the scope or spirit of the invention. Other embodiments of the invention will be apparent to those skilled in the art from consideration of the specification and practice of the invention disclosed herein. It is intended that the specification and examples be considered as exemplary only, with a true scope and spirit of the invention being indicated by the following claims.

The entire disclosure in the complete specification of our Australian Patent Application No. 2002341938 is by this cross-reference incorporated into the present specification.

O

0 0

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Claims (2)

1. 2. A transgenic animal according to claim 1, wherein the transgenic animal 0expresses a nucleic acid encoding the peptide of SEQ ID NO:8.
2. 3. A transgenic animal according to claim 1, substantially as herein described C 10 with reference to the examples and/or figures.