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大鼠脑中的多巴胺D2受体:使用高亲和力选择性激动剂配体的放射自显影可视化

Dopamine D2 receptors in the rat brain: autoradiographic visualization using a high-affinity selective agonist ligand.

作者信息

Charuchinda C, Supavilai P, Karobath M, Palacios J M

出版信息

J Neurosci. 1987 May;7(5):1352-60. doi: 10.1523/JNEUROSCI.07-05-01352.1987.

DOI:10.1523/JNEUROSCI.07-05-01352.1987
PMID:2437261
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6568828/
Abstract

The non-catechol, selective dopamine D2-agonist compound 3H-205-502 was used to localize dopamine D2 receptors by autoradiography after in vitro labeling of brain sections. The characteristics of the binding of this ligand to tissue sections were those expected from the labeling of dopamine D2 receptors. The binding of 3H-205-502 was inhibited selectively and stereospecifically by dopamine D2 agents but not by dopamine D1 compounds. The autoradiographic localization of 3H-205-502 binding sites showed high densities of dopamine D2 receptors in areas such as the glomerular layer of the olfactory bulb, the nucleus accumbens, caudate-putamen, olfactory tubercle, the lateral septum, and the islands of Calleja. Besides these dopamine-innervated areas the substantia nigra and the ventral tegmental area also showed important receptor densities. Other areas where dopamine D2 receptor binding was found were the stratum lacunosum-moleculare of the hippocampus, bands of labeling in the molecular layer of the 9th and 10th lobules of the cerebellum, and several components of the visual system. This distribution presents similarities and differences with previously reported distributions of dopamine D2 receptors visualized autoradiographically using 3H-labeled agonists and antagonists. In view of the high affinity, guanine nucleotide insensitivity, and dopamine D2 selectivity of this agonist ligand, it is suggested that dopamine D2 receptors exist in different states in different areas. 3H-205-502 appears to be a new and useful tool for the study of dopamine D2 receptors.

摘要

非儿茶酚类选择性多巴胺D2激动剂化合物3H-205-502,在体外标记脑切片后,通过放射自显影法用于定位多巴胺D2受体。该配体与组织切片结合的特性,是多巴胺D2受体标记所预期的。3H-205-502的结合被多巴胺D2药物选择性地和立体特异性地抑制,但不被多巴胺D1化合物抑制。3H-205-502结合位点的放射自显影定位显示,在嗅球的肾小球层、伏隔核、尾状核-壳核、嗅结节、外侧隔和Calleja岛等区域,多巴胺D2受体密度很高。除了这些多巴胺神经支配区域外,黑质和腹侧被盖区也显示出重要的受体密度。发现多巴胺D2受体结合的其他区域包括海马的腔隙分子层、小脑第9和第10小叶分子层的标记带,以及视觉系统的几个组成部分。这种分布与先前报道的使用3H标记的激动剂和拮抗剂通过放射自显影观察到的多巴胺D2受体分布既有相似之处,也有不同之处。鉴于这种激动剂配体具有高亲和力、对鸟嘌呤核苷酸不敏感以及对多巴胺D2的选择性,提示多巴胺D2受体在不同区域以不同状态存在。3H-205-502似乎是研究多巴胺D2受体的一种新的有用工具。

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