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通过突触前终末再摄取机制实现α-1和α-2去甲肾上腺素受体功能分离的证据。

Evidence for functional separation of alpha-1 and alpha-2 noradrenaline receptors by pre-synaptic terminal re-uptake mechanisms.

作者信息

Clark A J, Butcher S P, Winn P

机构信息

Psychological Laboratory, University of St. Andrews, Fife, UK.

出版信息

Psychopharmacology (Berl). 1991;103(3):366-74. doi: 10.1007/BF02244291.

Abstract

Information transfer within the central nervous system is predominantly chemical in nature, and occurs both through synaptic specialisations and non-specific diffuse release. The localisation and description of receptors for these two types of neurotransmission is currently a contentious issue. In the present study, the noradrenaline reuptake inhibitor cocaine has been shown to overcome the inhibitory effects of idazoxan, a selective alpha-2 receptor antagonist, but not phentolamine, a non-selective alpha receptor antagonist, on eating following injection of noradrenaline into the rat hypothalamic paraventricular nucleus. Similarly, lesion by 6-hydroxydopamine of noradrenaline terminals in the paraventricular nucleus also reduced the efficacy of idazoxan in blocking eating induced by noradrenaline. These data confirm that postsynaptic alpha-2 receptors are involved in the feeding response to exogenous noradrenaline, but in addition, when taken in conjunction with previously published data, are used to suggest a differential distribution of NA receptors within the hypothalamic paraventricular nucleus. It is proposed that the alpha-2 subtype may be extrasynaptic, the alpha-1 subtype intrasynaptic.

摘要

中枢神经系统内的信息传递本质上主要是化学性的,通过突触特化和非特异性扩散释放两种方式发生。这两种神经传递类型的受体定位和描述目前是一个有争议的问题。在本研究中,已表明去甲肾上腺素再摄取抑制剂可卡因能够克服选择性α-2受体拮抗剂咪唑克生,但不能克服非选择性α受体拮抗剂酚妥拉明对向大鼠下丘脑室旁核注射去甲肾上腺素后进食的抑制作用。同样,用6-羟基多巴胺损毁室旁核中的去甲肾上腺素终末也降低了咪唑克生阻断去甲肾上腺素诱导进食的效力。这些数据证实,突触后α-2受体参与对外源性去甲肾上腺素的进食反应,但此外,结合先前发表的数据,这些数据被用来提示去甲肾上腺素受体在下丘脑室旁核内的分布存在差异。有人提出,α-2亚型可能位于突触外,α-1亚型位于突触内。

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