April 8, 2005

Protein’s role in heart attack damage studied

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Mark Anderson, M.D., Ph.D., Roger Colbran, Ph.D., and Rong Zhang, M.D./Ph.D.
photo by Dana Johnson

Protein’s role in heart attack damage studied

Mice with glowing green hearts have yielded the latest clue in the search for molecules involved in structural heart disease. Vanderbilt investigators found that blocking the activity of a single protein, called CaM kinase, in the mouse heart protects against the damaging effects of a heart attack.

The findings, published in the April issue of Nature Medicine, suggest that medicines designed to block CaM kinase activity may be useful for treating patients with structural heart disease and myocardial dysfunction.

Heart disease remains the number one killer in the United States. Most of that disease is in individuals who have suffered a heart attack or who have had changes in the heart muscle, including hypertrophy and dilation, for other reasons, said Mark E. Anderson, M.D., Ph.D., Betty and Jack Bailey Professor of Cardiovascular Medicine and the senior investigator of the current study.

“People with structural heart disease die suddenly from electrical instability — arrhythmias — and also because the heart fails to function properly as a pump,” said Anderson, who is also associate professor of Medicine and Pharmacology.

Anderson and Roger J. Colbran, Ph.D., associate professor of Molecular Physiology & Biophysics, have collaborated for a number of years to study the role of the protein CaM kinase in signaling pathways that underlie the heart's electrical stability and maintenance of normal rhythm. Several years ago, they demonstrated in a mouse model of cardiac hypertrophy that blocking CaM kinase activity suppresses arrhythmias.

At the same time, evidence from other laboratories began to suggest that CaM kinase's role in structural heart disease went beyond the electrical signaling network. CaM kinase protein was consistently elevated in patients and animals with structural heart disease. And mouse lines genetically engineered to produce excess CaM kinase developed a convincing model of structural heart disease — the hearts thickened, then dilated, and the animals died suddenly, Anderson said.

“We were interested in closing the loop: if we targeted CaM kinase for inhibition, could we prevent or reduce structural heart disease phenotypes that were relevant in patients?” Anderson asked.

Because existing CaM kinase inhibitor drugs affect a number of different targets, the investigators opted to use a genetic approach to block CaM kinase activity. Rong Zhang, M.D., Ph.D., research assistant professor of Medicine, engineered mice to express a peptide inhibitor of the kinase protein, or a control peptide that did not block the kinase, only in heart cells, and only after birth. Zhang linked the peptide inhibitor and the control peptide to a green fluorescent protein to confirm expression in heart, giving the engineered mouse hearts a green glow.

The researchers surgically created large heart attacks and studied how the hearts responded. In non-engineered mice and mice with control peptide, the hearts underwent structural remodeling — the surviving heart muscle thickened and hypertrophied in an attempt to compensate, then it dilated and failed. Mice expressing CaM kinase inhibitor fared better.

“The mice with genetic CaM kinase inhibition didn't undergo such severe remodeling and their cardiac function remained substantially improved,” Anderson said.

Systemic administration of a CaM kinase inhibitor drug to non-engineered mice had a similar effect.

The investigators then isolated and dissociated surviving heart muscle cells and found that the cells from mice with inhibited CaM kinase — either genetic or pharmacologic — managed calcium in a way that looked more normal and had highly preserved contraction and relaxation responses compared to cardiac cells from mice without inhibited CaM kinase.

“Our data suggest that the activity of CaM kinase is enough to make several of the 'bad' phenotypes in common heart disease: the dilation, dysfunction, and lack of ability to manage intracellular calcium. And by inhibiting CaM kinase, you can preserve and shift many of those functions toward more normal levels,” Anderson said.

The cardiac cells with CaM kinase inhibition retained a complete ability to respond to the drug isoproterenol, which activates the beta adrenergic receptor, part of the physiological “fight or flight” response to adrenaline. This finding is important, Anderson said, as it suggests that the heart muscle retains normal physiological responses even when CaM kinase is inhibited for a long period of time.

“There's a huge unmet need for drugs to treat individuals with structural heart disease,” Anderson said. “The two-pronged worry in these patients is electrical instability leading to arrhythmias and mechanical dysfunction leading to heart failure. CaM kinase inhibition could address both concerns.”

Anderson has been working with a company to develop CaM kinase inhibitor drugs, and his laboratory is currently testing several new candidates.

Rong Zhang, M.D., Ph.D., Michelle S. C. Khoo, M.D., Yuejin Wu, Ph.D., and Yingbo Yang, M.D., Ph.D., are the lead authors of the Nature Medicine paper. The research was supported by the National Institutes of Health and the American Heart Association.