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α2肾上腺素能受体在血管平滑肌中的突触后定位:清醒兔的体内研究

A postsynaptic location of alpha 2 adrenoceptors in vascular smooth muscle: in vivo studies in the conscious rabbit.

作者信息

Hamilton C A, Reid J L

出版信息

Cardiovasc Res. 1982 Jan;16(1):11-5. doi: 10.1093/cvr/16.1.11.

Abstract

The rise in blood pressure after intravenous administration of a range of alpha-adrenoceptor agonists and the effect of alpha adrenoceptor antagonists was studied in groups of conscious rabbits. Phentolamine was equally effective at blocking the pressor response to the alpha 1 adrenoceptor agonist phenylephrine and the mixed alpha 1/alpha 2 adrenoceptor agonist noradrenaline. Phenoxybenzamine which acts preferentially on alpha 1 adrenoceptors and the more specific alpha 1 adrenoceptor antagonist prazosin were more effective against phenylephrine induced rises in pressure, while yohimbine and alpha yohimbine which preferentially act on alpha 2 adrenoceptors were more effective against noradrenaline. The immediate pressor response to intravenous injections of the alpha 2 adrenoceptor agonists clonidine and guanabenz was blocked more effectively by phentolamine than prazosin when doses which gave a postsynaptic location of both alpha 1 and alpha 2 adrenoceptors both of which mediate vasoconstrictor responses in vascular smooth muscle.

摘要

在清醒兔组中研究了静脉注射一系列α-肾上腺素能受体激动剂后血压的升高以及α-肾上腺素能受体拮抗剂的作用。酚妥拉明在阻断对α1肾上腺素能受体激动剂去氧肾上腺素和α1/α2混合肾上腺素能受体激动剂去甲肾上腺素的升压反应方面同样有效。优先作用于α1肾上腺素能受体的酚苄明和更具特异性的α1肾上腺素能受体拮抗剂哌唑嗪在对抗去氧肾上腺素引起的血压升高方面更有效,而优先作用于α2肾上腺素能受体的育亨宾和α-育亨宾在对抗去甲肾上腺素方面更有效。当给予能使α1和α2肾上腺素能受体都位于突触后位置(两者均介导血管平滑肌中的血管收缩反应)的剂量时,酚妥拉明比哌唑嗪更有效地阻断了静脉注射α2肾上腺素能受体激动剂可乐定和胍那苄后的即时升压反应。

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