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吗茚酮、甲氧氯普胺和多潘立酮对大鼠纹状体中[3H]螺哌啶结合位点类别的差异亲和力:药理学上不同受体类别的证据。

Differential affinities of molindone, metoclopramide and domperidone for classes of [3H]spiroperidol binding sites in rat striatum: evidence for pharmacologically distinct classes of receptors.

作者信息

Rosenfeld M R, Dvorkin B, Klein P N, Makman M H

出版信息

Brain Res. 1982 Mar 4;235(1):205-11. doi: 10.1016/0006-8993(82)90214-1.

Abstract

Rat striatum contains two populations of dopaminergic [3H]spiroperidol binding sites. The two populations are similar in their affinities for chlorpromazine and dopamine. Only one population, that with a somewhat higher affinity for spiroperidol itself, exhibits high affinity for the selective D2 antagonists molindone, metoclopramide and domperidone. Hence, this population may represent D2 receptor sites. The other larger population may represent either a separate class of receptor sites or a different form of D2 receptor sites.

摘要

大鼠纹状体含有两类多巴胺能[3H]螺哌啶结合位点。这两类位点对氯丙嗪和多巴胺的亲和力相似。只有一类位点,即对螺哌啶本身亲和力稍高的那类,对选择性D2拮抗剂吗茚酮、甲氧氯普胺和多潘立酮表现出高亲和力。因此,这类位点可能代表D2受体位点。另一类数量较多的位点可能代表另一类受体位点,或者是D2受体位点的不同形式。

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