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Am J Physiol Cell Physiol 291: C348-C356, 2006. First published March 29, 2006; doi:10.1152/ajpcell.00086.2006
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MEMBRANE TRANSPORTERS, ION CHANNELS, AND PUMPS

Kv2 channels oppose myogenic constriction of rat cerebral arteries

Gregory C. Amberg and Luis F. Santana

Department of Physiology and Biophysics, University of Washington, Seattle, Washington

Submitted 21 February 2006 ; accepted in final form 22 March 2006

By hyperpolarizing arterial smooth muscle, voltage-gated, Ca2+-independent K+ (Kv) channels decrease calcium influx and thus oppose constriction. However, the molecular nature of the Kv channels function in arterial smooth muscle remains controversial. Recent investigations have emphasized a predominant role of Kv1 channels in regulating arterial tone. In this study, we tested the hypothesis Kv2 channels may also significantly regulate tone of rat cerebral arteries. We found that Kv2.1 transcript and protein are present in cerebral arterial smooth muscle. In addition, our analysis indicates that a substantial component ({approx}50%) of the voltage dependencies and kinetics of Kv currents in voltage-clamped cerebral arterial myocytes is consistent with Kv2 channels. Accordingly, we found that stromatoxin, a specific inhibitor of Kv2 channels, significantly decreased Kv currents in these cells. Furthermore, stromatoxin enhanced myogenic constriction of pressurized arterial segments. We also found that during angiotensin II-induced hypertension, Kv2 channel function was reduced in isolated myocytes and in intact arteries. This suggests that impaired Kv2 channel activity may contribute to arterial dysfunction during hypertension. On the basis of these novel observations, we propose a new model of Kv channel function in arterial smooth muscle in which Kv2 channels (in combination with Kv1 channels) contribute to membrane hyperpolarization and thus oppose constriction.

smooth muscle; potassium channels; hypertension



Address for reprint requests and other correspondence: L. F. Santana, Dept. of Physics and Biophysics, Univ. of Washington, PO Box 357290, Seattle, WA 98195 (e-mail: santana{at}u.washington.edu)




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