Characterization of α2-adrenoceptors in smooth muscles of the spontaneously hypertensive rat aorta

被引:3
作者
Fauaz, G [1 ]
Feres, T [1 ]
Farias, NC [1 ]
Paiva, ACM [1 ]
Paiva, TB [1 ]
机构
[1] Univ Fed Sao Paulo, Escola Paulista Med, Dept Biophys, BR-04023032 Sao Paulo, SP, Brazil
基金
巴西圣保罗研究基金会;
关键词
SHR; rat aorta; membrane potential; alpha(2)-adrenoceptor; Ca2+-dependent K+ channel; UK 14,304;
D O I
10.1016/S1537-1891(03)00002-8
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Previous works have shown that the alpha(2)-adrenoceptor agonist UK 14,304 induced the relaxation and hyperpolarization of the rat aorta, mediated by alpha(2)-adrenoceptors present in the smooth muscles, through small-conductance, ATP-sensitive K+ channels. We now report that in spontaneously hypertensive rat (SHR) aortic rings, UK 14,304 induced concentration-dependent hyperpolarizing responses, which were inhibited by yohimbine, an alpha2-adrenoceptor inhibitor, and by glibenclamide, a specific inhibitor of small-conductance, ATP-sensitive K+ channels. The responses were also partially inhibited by iberiotoxin and by apamin. Treatment with N-omega-nitro-L-arginine (L-NNA) did not affect the response to UK 14,304. These results indicate that alpha(2)-adrenoceptors are present in SHR aortic smooth muscle cell membranes, but differ from those of normotensive animals regarding the K+ channels involved in their responses. Moreover, the resting membrane potential (RMP) was significantly more negative in SHR than in normotensive rats. This relative hyperpolarized state is probably due to Cat(2+)-dependent K+ channels being constitutively open in SHR, since the addition of iberiotoxin caused a significant depolarization of the aortic smooth muscle membranes in this strain. (C) 2003 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:127 / 131
页数:5
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