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Am J Physiol Heart Circ Physiol 292: H1906-H1916, 2007. First published December 8, 2006; doi:10.1152/ajpheart.00793.2006
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Chronic verapamil treatment remodels ICa,L in mouse ventricle

Elizabeth Schroder,1 Janos Magyar,1 Don Burgess,2 Douglas Andres,3 and Jonathan Satin1

1Department of Physiology, University of Kentucky, Lexington; 2Department of Physics, Asbury College, Wilmore; and 3Department of Molecular and Cellular Biochemistry, University of Kentucky, Lexington, Kentucky

Submitted 24 July 2006 ; accepted in final form 5 December 2006

In this study we tested the hypothesis that ventricular homeostasis of L-type Ca2+ current (ICa,L) minimally involves regulation of the main pore-forming {alpha}-subunit (CaV1.2) and auxiliary proteins that serve as positive or negative regulators of ICa,L. We treated animals for 24 h with verapamil (Ver, 3.6 mg·kg–1·day–1), isoproterenol (Iso, 30 mg·kg–1·day–1), or Iso + Ver via osmotic minipumps. To test for alterations of Ca2+ channel complex components we performed real-time PCR and Western blot analysis on ventricle. In addition, cardiac myocytes (CMs) were dispersed and current was recorded in the whole cell configuration to evaluate ICa,L. Surprisingly, 24- to 48-h Ver increased CaV1.2 mRNA and protein and ICa,L current (Ver 11 ± 1pA/pF vs. control 7 ± 0.5pA/pF; P < 0.01). ICa,L from CMs in Ver mice showed no change in whole cell capacitance. To examine the in vivo effects of a physiologically relevant Ca2+ channel agonist, we treated mice with Iso. Twenty-four-hour Iso infusion increased heart rate; CaV1.2- and CaVbeta2 mRNA levels were constant, but the Ca2+ channel subunit mRNA Rem was increased twofold. Cells isolated from 24-h Iso hearts showed no change in basal ICa,L density and diminished responsiveness to acute 1 µM Iso. To further examine the homeostatic regulation of the Ca2+ channel, we treated animals for 24 h with Iso + Ver. The influence of Iso + Ver was similar that of to Iso alone on Ca2+ channel mRNAs and ICa,L, with the exception that it prevented the increase in Rem seen with Iso treatment. Long-term Ca2+ channel blockade induces an increase of CaV1.2 mRNA and protein and significantly increases ICa,L.

calcium channel blockade; ventricle; electrocardiogram; electrophysiology



Address for reprint requests and other correspondence: E. Schroder, Univ. of Kentucky, Dept. of Physiology, 800 Rose St., MS508, Lexington, KY 40536-0298 (e-mail: eschr0{at}uky.edu)




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E. Schroder, M. Byse, and J. Satin
L-Type Calcium Channel C Terminus Autoregulates Transcription
Circ. Res., June 19, 2009; 104(12): 1373 - 1381.
[Abstract] [Full Text] [PDF]




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