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The L-type calcium channel inhibitor diltiazem prevents cardiomyopathy in a mouse model
Christopher Semsarian, Imran Ahmad, Michael Giewat, Dimitrios Georgakopoulos, Joachim P. Schmitt, Bradley K. McConnell, Steven Reiken, Ulrike Mende, Andrew R. Marks, David A. Kass, Christine E. Seidman, J.G. Seidman
Christopher Semsarian, Imran Ahmad, Michael Giewat, Dimitrios Georgakopoulos, Joachim P. Schmitt, Bradley K. McConnell, Steven Reiken, Ulrike Mende, Andrew R. Marks, David A. Kass, Christine E. Seidman, J.G. Seidman
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Article Genetics

The L-type calcium channel inhibitor diltiazem prevents cardiomyopathy in a mouse model

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Abstract

Dominant mutations in sarcomere protein genes cause hypertrophic cardiomyopathy, an inherited human disorder with increased ventricular wall thickness, myocyte hypertrophy, and disarray. To understand the early consequences of mutant sarcomere proteins, we have studied mice (designated αMHC403/+) bearing an Arg403Gln missense mutation in the α cardiac myosin heavy chain. We demonstrate that Ca2+ is reduced in the sarcoplasmic reticulum of αMHC403/+ mice, and levels of the sarcoplasmic reticulum Ca2+-binding protein calsequestrin are diminished in advance of changes in cardiac histology or morphology. Further evidence for dysregulation of sarcoplasmic reticulum Ca2+ in these animals is seen in their decreased expression of the ryanodine receptor Ca2+-release channel and its associated membrane proteins and in an increase in ryanodine receptor phosphorylation. Early administration of the L-type Ca2+ channel inhibitor diltiazem restores normal levels of these sarcoplasmic reticular proteins and prevents the development of pathology in αMHC403/+ mice. We conclude that disruption of sarcoplasmic reticulum Ca2+ homeostasis is an important early event in the pathogenesis of this disorder and suggest that the use of Ca2+ channel blockers in advance of established clinical disease could prevent hypertrophic cardiomyopathy caused by sarcomere protein gene mutations.

Authors

Christopher Semsarian, Imran Ahmad, Michael Giewat, Dimitrios Georgakopoulos, Joachim P. Schmitt, Bradley K. McConnell, Steven Reiken, Ulrike Mende, Andrew R. Marks, David A. Kass, Christine E. Seidman, J.G. Seidman

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Figure 5

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Model of Ca2+ cycling in cardiac myocytes and the effects of a hypertrop...
Model of Ca2+ cycling in cardiac myocytes and the effects of a hypertrophic cardiomyopathy–causing mutation. (a) Wild-type myocytes showing normal Ca2+ regulation. Ca2+ enters the myocyte through L-type Ca2+ channels. Small entry of Ca2+ stimulates Ca release (calcium-induced Ca2+ release; CICR) from the SR via cardiac ryanodine receptors (RyR2) to the sarcomere. Ca2+ returns to the SR via the sarcoplasmic/endoplasmic Ca2+ ATPase (SERCA) pump, which is regulated by phospholamban (PLB). Ca2+ cycling is “balanced” between the sarcomere and SR. (b) Mutant (αMHC403/+) myocytes have a mutation in the sarcomere (represented by an asterisk). The defective sarcomere acts as an ion trap, resulting in accumulation of Ca2+. Less Ca2+ returns to the SR, resulting in decreased SR Ca2+ stores, decreased SR calsequestrin (CSQ), and reduced expression of RyR2. The net effect is a Ca2+ shift within the cell, with a relative Ca2+ excess in the sarcomere, and Ca2+ depletion in the SR.

Copyright © 2026 American Society for Clinical Investigation
ISSN: 0021-9738 (print), 1558-8238 (online)

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