McGrath J C
Biochem Pharmacol. 1982 Feb 15;31(4):467-84. doi: 10.1016/0006-2952(82)90147-2.
The concept of two types of alpha-adrenoceptor, alpha 1 located on smooth muscle and mediating contraction and alpha 2 located on nerve terminals and mediating inhibition of transmitter release, has broken down. In vivo it has been shown that post-junctional receptors, with characteristics closely related to those of the alpha 2-adrenoceptors at nerve terminals, can mediate pressor responses and are, "post-junctional alpha 2-adrenoceptors". Several differences among agonists in vitro have superficial similarities to the in vivo alpha 1/alpha 2 system but do not correspond precisely and seem to point to a subdivision of post-junctional alpha 1-adrenoceptors. A preliminary hypothesis is: in vivo alpha 1 is rapid in onset, short-lived, utilises internal Ca2+, prefers alkalosis and responds to short-term stimuli such as short bursts of nerve impulses or bolus injections of catecholamines; alpha 2 is slower in onset, longer-lived, utilises external Ca2+, prefers acidosis and responds to more prolonged stimuli such as circulating catecholamines; in vitro these categories of response occur but antagonists fail to define an alpha 1/alpha 2 split, suggesting that some critical factor is missing in vitro. The implications of these trends in alpha-adrenoceptor classification are discussed in relation to current pharmacological and biochemical methods for receptor typing, to the possible physiological actions and roles of such receptors and to structure/activity relationships among agonists and antagonists.
两种α-肾上腺素能受体的概念已经瓦解,这两种受体分别是位于平滑肌上介导收缩作用的α1受体以及位于神经末梢上介导递质释放抑制作用的α2受体。在体内研究表明,具有与神经末梢α2-肾上腺素能受体密切相关特性的节后受体,能够介导升压反应,即“节后α2-肾上腺素能受体”。体外实验中几种激动剂之间的差异与体内α1/α2系统有表面上的相似性,但并不完全对应,似乎表明节后α1-肾上腺素能受体存在细分。一个初步假设是:在体内,α1受体起效迅速、作用短暂,利用细胞内Ca2+,偏好碱中毒,对短期刺激如短串神经冲动或儿茶酚胺推注有反应;α2受体起效较慢、作用持久,利用细胞外Ca2+,偏好酸中毒,对更持久的刺激如循环中的儿茶酚胺有反应;在体外,这些反应类型存在,但拮抗剂无法明确区分α1/α2,这表明体外缺少某些关键因素。本文结合当前用于受体分型的药理和生化方法、此类受体可能的生理作用和角色以及激动剂和拮抗剂之间的构效关系,讨论了这些α-肾上腺素能受体分类趋势的意义。