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α肾上腺素能受体在勃起功能中的作用。

Role of alpha adrenergic receptors in erectile function.

作者信息

Traish A, Kim N N, Moreland R B, Goldstein I

机构信息

Department of Urology, Boston University School of Medicine, MA 02118, USA.

出版信息

Int J Impot Res. 2000 Mar;12 Suppl 1:S48-63.

Abstract

Penile erection is a complex physiological process in which the regulation of penile hemodynamics depends on signal input from central and peripheral nervous systems, and on the balance and interplay between several local physiological mediators (neurotransmitters, vasoactive agents and endocrine factors). A role for the sympathetic nervous system in attaining or maintaining penile flaccidity and detumescence is well recognized. However, the exact mechanisms of alpha-adrenergic receptor mediated erectile function remain poorly defined. The objective of this review is to summarize data presented in the literature and from our laboratory on alpha-adrenergic receptors, and to discuss the conceptual framework by which the alpha-adrenergic receptor pathway modulates penile corpus cavernosum smooth muscle contractility. We will integrate the current state of knowledge of penile erection into one framework encompassing the biochemical and physiological pathways responsible for trabecular smooth muscle relaxation (erection) and contraction (detumescence). We will focus our discussion on local control mechanisms of alpha-adrenergic receptors and explore the following topics: (1) functional activity of alpha-1 and alpha-2 adrenergic receptors in the physiology of human penile erection; (2) identification, classification and characterization of alpha-1 and alpha-2 adrenergic receptor subtypes in human penile erectile tissue; (3) molecular mechanism of action of alpha-1 and alpha-2 adrenergic receptors in human penile erectile tissue; (4) blockade of alpha-1 and alpha-2 adrenergic receptor action by selective and non-selective alpha-1 and alpha-2 adrenergic receptor antagonists (blockers); (5) physiologic (functional) antagonism of alpha-1 and alpha-2 adrenergic receptor activity by vasodilators mediating smooth muscle relaxation; and (6) key areas of consensus, as well as critical gaps in the existing scientific knowledge concerning the rationale and the potential use of alpha-blockers in erectile function.

摘要

阴茎勃起是一个复杂的生理过程,其中阴茎血流动力学的调节取决于来自中枢和外周神经系统的信号输入,以及几种局部生理介质(神经递质、血管活性物质和内分泌因子)之间的平衡与相互作用。交感神经系统在实现或维持阴茎疲软和消肿方面的作用已得到充分认可。然而,α-肾上腺素能受体介导勃起功能的确切机制仍不清楚。本综述的目的是总结文献和我们实验室提供的关于α-肾上腺素能受体的数据,并讨论α-肾上腺素能受体途径调节阴茎海绵体平滑肌收缩性的概念框架。我们将把阴茎勃起的当前知识状态整合到一个框架中,该框架涵盖负责小梁平滑肌松弛(勃起)和收缩(消肿)的生化和生理途径。我们将把讨论重点放在α-肾上腺素能受体的局部控制机制上,并探讨以下主题:(1)α-1和α-2肾上腺素能受体在人类阴茎勃起生理学中的功能活性;(2)人类阴茎勃起组织中α-1和α-2肾上腺素能受体亚型的鉴定、分类和特征;(3)α-1和α-2肾上腺素能受体在人类阴茎勃起组织中的分子作用机制;(4)选择性和非选择性α-1和α-2肾上腺素能受体拮抗剂(阻滞剂)对α-1和α-2肾上腺素能受体作用的阻断;(5)介导平滑肌松弛的血管扩张剂对α-1和α-2肾上腺素能受体活性的生理(功能)拮抗作用;以及(6)关于α-阻滞剂在勃起功能中的原理和潜在用途的现有科学知识中的共识关键领域以及关键差距。

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