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毛细血管前血管:交感神经系统和儿茶酚胺的作用。

Precapillary vessels: effects of the sympathetic nervous system and of catecholamines.

作者信息

Alabaster V, Davey M

出版信息

J Cardiovasc Pharmacol. 1984;6 Suppl 2:S365-76.

PMID:6206345
Abstract

The study of receptor-operated control mechanisms involved in adrenergic transmission in the blood vessel wall has substantially advanced the understanding of the factors involved in the maintenance of arteriolar tone. As a result of this work, alpha-adrenoreceptors have been divided into two major subtypes termed alpha 1- and alpha 2-adrenoreceptors. Initially, the term alpha 1 was proposed as a synonym for the postjunctional alpha-adrenoreceptor. There is now a large body of evidence for the existence of postjunctional alpha-adrenoreceptors mediating the contraction of vascular smooth muscles that are resistant to blockade by the alpha 1-adrenoreceptor antagonist prazosin, but are blocked by alpha 2-antagonists and can be activated by selective alpha 2-agonists but not by selective alpha 1-agonists. The physiological significance of postjunctional alpha 2-adrenoreceptors is discussed in respect to factors such as their role in blood pressure control and of whether they are innervated or not, and the differences in contractile responses and in the postreceptor mechanisms involved in stimulation-contraction coupling following activation of each receptor subtype are reviewed. Although the situation is complex, on balance the data are compatible with the view that alpha 2-adrenoreceptor-mediated responses in vascular smooth muscle are more dependent on the physiological environment than are responses mediated by alpha 1-adrenoceptors. Thus, although postjunctional alpha 2-adrenoreceptors can be involved in sympathetic nerve transmission, they appear largely to fulfill a humoral role in vascular smooth muscle closely allied to the prevailing conditions, whereas alpha 1-adrenoreceptors are primarily involved in sympathetic neurotransmission, independent of local environmental conditions.

摘要

对血管壁肾上腺素能传递中受体介导的控制机制的研究,极大地推动了我们对参与维持小动脉张力的因素的理解。这项研究工作的结果是,α-肾上腺素受体已被分为两个主要亚型,即α1-和α2-肾上腺素受体。最初,α1这个术语被提议作为节后α-肾上腺素受体的同义词。现在有大量证据表明,存在节后α-肾上腺素受体,它介导血管平滑肌的收缩,这种收缩对α1-肾上腺素受体拮抗剂哌唑嗪的阻断具有抗性,但可被α2-拮抗剂阻断,并且可被选择性α2-激动剂激活,而不能被选择性α1-激动剂激活。本文讨论了节后α2-肾上腺素受体在血压控制等因素方面的生理意义,以及它们是否受神经支配,并且综述了每种受体亚型激活后在刺激-收缩偶联中涉及的收缩反应和受体后机制的差异。尽管情况复杂,但总体而言,数据与以下观点相符:血管平滑肌中α2-肾上腺素受体介导的反应比α1-肾上腺素受体介导的反应更依赖于生理环境。因此,尽管节后α2-肾上腺素受体可能参与交感神经传递,但它们在血管平滑肌中似乎主要发挥与当前条件密切相关的体液作用,而α1-肾上腺素受体主要参与交感神经传递,独立于局部环境条件。

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