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Abnormal Coronary Function in Mice Deficient in 1H T-type Ca2+ Channels
Chien-Chang Chen,1,2
Kathryn G. Lamping,4,5,7
Daniel W. Nuno,4,5,7
Rita Barresi,1,2
Sally J. Prouty,1,2
Julie L. Lavoie,4
Leanne L. Cribbs,8
Sarah K. England,2
Curt D. Sigmund,4
Robert M. Weiss,4,7
Roger A. Williamson,6
Joseph A. Hill,9
Kevin P. Campbell1,2,3*
Abstract:
Calcium ion (Ca2+) influx through voltage-gated Ca2+ channelsis important for the regulation of vascular tone. Activationof L-type Ca2+ channels initiates muscle contraction; however,the role of T-type Ca2+ channels (T-channels) is not clear.We show that mice deficient in the 1H T-type Ca2+ channel (13.2-null)have constitutively constricted coronary arterioles and focalmyocardial fibrosis. Coronary arteries isolated from 13.2-nullarteries showed normal contractile responses, but reduced relaxationin response to acetylcholine and nitroprusside. Furthermore,acute blockade of T-channels with Ni2+ prevented relaxationof wild-type coronary arteries. Thus, Ca2+ influx through 1HT-type Ca2+ channels is essential for normal relaxation of coronaryarteries.
1 Howard Hughes Medical Institute, University of Iowa, Iowa City, IA 52242, USA. 2 Department of Physiology and Biophysics, University of Iowa, Iowa City, IA 52242, USA. 3 Department of Neurology, University of Iowa, Iowa City, IA 52242, USA. 4 Department of Internal Medicine, University of Iowa, Iowa City, IA 52242, USA. 5 Department of Pharmacology, University of Iowa, Iowa City, IA 52242, USA. 6 Department of Obstetrics and Gynecology, University of Iowa, Iowa City, IA 52242, USA. 7 Veterans Administration Medical Center, Iowa City, IA 52242, USA. 8 Cardiovascular Institute, Loyola University Medical Center, 2160 South First Avenue, Maywood, IL 60153, USA. 9 Division of Cardiology, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.
* To whom correspondence should be addressed. E-mail: kevin-campbell{at}uiowa.edu
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