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去大脑大鼠交感缩血管反应中α-肾上腺素能受体介导成分及其他成分的分析。

Analysis of the alpha-adrenoceptor-mediated, and other, components in the sympathetic vasopressor responses of the pithed rat.

作者信息

Flavahan N A, Grant T L, Greig J, McGrath J C

出版信息

Br J Pharmacol. 1985 Sep;86(1):265-74. doi: 10.1111/j.1476-5381.1985.tb09458.x.

Abstract

The vascular receptors activated following sympatho-adrenal stimulation were determined by analysing the effects of 'selective' antagonists on the vasopressor response to spinal sympathetic nerve activation in the pithed rat. The net vascular response to adrenal stimulation was a balance between alpha-adrenoceptor-mediated vasoconstriction and beta-adrenoceptor-mediated vasodepression. Part of the alpha-adrenoceptor-mediated response was 'prazosin-sensitive' (alpha 1) and the remainder was abolished by rauwolscine (alpha 2). As with adrenal stimulation, direct sympathetic nerve stimulation of the vasculature evoked pressor responses which were partly resistant to prazosin. Rauwolscine only partly blocked the prazosin-sensitive component. Reserpine pretreatment led to smaller responses than prazosin plus rauwolscine. Thus, the response resistant to alpha-adrenoceptor antagonists could be mediated, in part, by adrenoceptors distinct from alpha-adrenoceptors, as currently defined. alpha, beta-Methylene ATP reduced the nerve-mediated pressor response after alpha-adrenoceptor blockade or reserpine pretreatment but not in drug-free controls. The results suggest that stimulation of the adrenal medulla can produce a vasopressor response which consists of summating alpha 1- and alpha 2-adrenoceptor-mediated components, and is identical to the effect of injected adrenaline. In contrast, the response to vasopressor nerve stimulation appears to be essentially mediated by alpha 1-adrenoceptors, with a facilitatory influence from alpha 2-adrenoceptors. A further response obtained after alpha-adrenoceptor blockade may contain a purinergic component and another which is adrenergic but not mediated by stimulation of alpha-adrenoceptors.

摘要

通过分析“选择性”拮抗剂对脊髓交感神经激活引起的升压反应的影响,确定了交感肾上腺刺激后激活的血管受体。对肾上腺刺激的净血管反应是α-肾上腺素能受体介导的血管收缩和β-肾上腺素能受体介导的血管舒张之间的平衡。α-肾上腺素能受体介导的反应部分是“哌唑嗪敏感的”(α1),其余部分被萝芙木碱(α2)消除。与肾上腺刺激一样,对血管系统的直接交感神经刺激引起的升压反应部分对哌唑嗪有抗性。萝芙木碱仅部分阻断了哌唑嗪敏感成分。利血平预处理导致的反应比哌唑嗪加萝芙木碱小。因此,对α-肾上腺素能受体拮抗剂有抗性的反应可能部分由不同于目前定义的α-肾上腺素能受体的肾上腺素能受体介导。α,β-亚甲基ATP在α-肾上腺素能受体阻断或利血平预处理后降低了神经介导的升压反应,但在无药物对照中没有降低。结果表明,肾上腺髓质的刺激可产生一种升压反应,该反应由α1-和α2-肾上腺素能受体介导的成分相加组成,与注射肾上腺素的效果相同。相比之下,对升压神经刺激的反应似乎基本上由α1-肾上腺素能受体介导,α2-肾上腺素能受体有促进作用。α-肾上腺素能受体阻断后获得的进一步反应可能包含嘌呤能成分和另一种肾上腺素能成分,但不是由α-肾上腺素能受体的刺激介导的。

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