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Characterization of alpha(2)-adrenoceptors in smooth muscles of the spontaneously hypertensive rat aorta.

机译:自发性高血压大鼠主动脉平滑肌中α(2)-肾上腺素受体的表征。

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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 alpha(2)-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 Ca(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.
机译:先前的研究表明,α(2)-肾上腺素受体激动剂UK 14,304通过小传导性,ATP敏感性K(+)诱导了平滑肌中存在的α(2)-肾上腺素受体介导的大鼠主动脉的松弛和超极化。 )频道。我们现在报告,在自发性高血压大鼠(SHR)主动脉环中,UK 14,304诱导了浓度依赖性超极化反应,该反应被约欣宾(一种α(2)-肾上腺素受体抑制剂)和格列本脲(一种小传导性特异性抑制剂)抑制, ATP敏感的K(+)通道。响应也被埃博毒素和阿帕明部分抑制。用N(ω)-硝基-L-精氨酸(L-NNA)治疗不会影响对UK 14,304的反应。这些结果表明,SHR主动脉平滑肌细胞膜中存在alpha(2)-肾上腺素能受体,但就其反应涉及的K(+)通道而言,与正常血压动物的受体不同。此外,SHR中的静息膜电位(RMP)显着高于血压正常大鼠。这种相对的超极化状态可能是由于SHR中的Ca(2+)依赖性K(+)通道组成性开放的,因为添加的毒素毒素导致该菌株中主动脉平滑肌膜明显去极化。

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