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纹状体和垂体中某些多巴胺受体复合物的定位与药理学:突触及非突触通讯

Localization and pharmacology of some dopamine receptor complexes in the striatum and the pituitary gland: synaptic and son-synaptic communication.

作者信息

Stoof J C

机构信息

Dept. of Neurology, Medical Faculty, Free University, Amsterdam, The Netherlands.

出版信息

Acta Morphol Neerl Scand. 1988;26(2-3):115-30.

PMID:2855385
Abstract

The striatum receives massive dopaminergic projections from neurons in the ventral tegmental area, the substantia nigra and the retro-rubral cell group. Dopaminergic neurons in the arcuate nucleus and periventricular hypothalamic nuclei project to the median eminence and the neuro-intermediate lobe of the pituitary gland. The anterior lobe of the pituitary gland is not innervated by dopaminergic neurons, but receives dopamine via a vascular route from the median eminence. Two categories of dopamine receptors (D-1 and D-2) can be identified on the basis of the ability of various drugs to discriminate between these two entities. Dopamine stimulates both D-1 and D-2 receptors. The affinity of dopamine for the D-2 receptor is approximately 1000 times higher than for the D-1 receptor. Dopamine is involved in synaptic as well as non-synaptic communication. Examples of non-synaptic communication via D-2 receptors are the dopamine induced inhibition of prolactin release from the anterior pituitary gland and most likely the D-2 receptor mediated inhibition of the release of acetylcholine in the striatum. Examples of synaptic communication have been found in the striatum where (with ultrastructural techniques) synaptic contacts between dopaminergic nerve terminals and elements from cells containing GABA, substance P or enkephalin have been demonstrated. It is tempting to speculate that synaptic and non-synaptic communication occurs via D-1 and D-2 receptors respectively.

摘要

纹状体接收来自腹侧被盖区、黑质和红核后细胞群神经元的大量多巴胺能投射。弓状核和室周下丘脑核中的多巴胺能神经元投射到正中隆起和垂体神经中间叶。垂体前叶不受多巴胺能神经元支配,但通过血管途径从正中隆起接收多巴胺。根据各种药物区分这两种实体的能力,可以识别出两类多巴胺受体(D-1和D-2)。多巴胺能刺激D-1和D-2受体。多巴胺对D-2受体的亲和力比对D-1受体高约1000倍。多巴胺参与突触和非突触通讯。通过D-2受体进行非突触通讯的例子有多巴胺诱导的垂体前叶催乳素释放抑制,以及很可能由D-2受体介导的纹状体乙酰胆碱释放抑制。在纹状体中发现了突触通讯的例子,其中(用超微结构技术)已证明多巴胺能神经末梢与含有γ-氨基丁酸、P物质或脑啡肽的细胞成分之间存在突触联系。很容易推测突触和非突触通讯分别通过D-1和D-2受体发生。

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