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Abnormal Coronary Function in Mice Deficient in 1H T-type Ca2+ Channels
Chien-Chang Chen,1,2Kathryn G. Lamping,4,5,7Daniel W. Nuno,4,5,7Rita Barresi,1,2Sally J. Prouty,1,2Julie L. Lavoie,4Leanne L. Cribbs,8Sarah K. England,2Curt D. Sigmund,4Robert M. Weiss,4,7Roger A. Williamson,6Joseph A. Hill,9Kevin P. Campbell1,2,3*
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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