Suppr超能文献

大鼠纹状体和海马中γ-羟基丁酸受体的定位研究。

Localization studies of gamma-hydroxybutyrate receptors in rat striatum and hippocampus.

作者信息

Hechler V, Gobaille S, Maitre M

机构信息

Centre de Neurochimie du CNRS, Strasbourg, France.

出版信息

Brain Res Bull. 1989 Jul-Aug;23(1-2):129-35. doi: 10.1016/0361-9230(89)90171-8.

Abstract

Quantitative autoradiography using [3H] gamma-hydroxybutyrate was used in combination with anatomic and neurotoxic lesions to localize the gamma-hydroxybutyrate (GHB) receptors in the striatum and hippocampus of rat brain. 6-Hydroxydopamine (6-OHDA) lesions of the nigro-striatal pathway failed to reduce [3H] gamma-hydroxybutyrate binding in the striatum. In contrast, kainic acid (KA) lesions of the caudate-putamen (CPu) resulted in about 45% loss of binding. For hippocampus, lesions of septo-hippocampal pathway did not modify receptor density but intrahippocampal kainic acid injection largely attenuated (50%) [3H] GHB binding. These results demonstrate that gamma-hydroxybutyrate receptors in the CPu and dorsal hippocampus are principally located on intrinsic neurons which may participate in the functional expression of the role gamma-hydroxybutyrate has in these structures.

摘要

利用[3H]γ-羟基丁酸进行定量放射自显影,并结合解剖学和神经毒性损伤,来定位大鼠脑纹状体和海马体中的γ-羟基丁酸(GHB)受体。黑质-纹状体通路的6-羟基多巴胺(6-OHDA)损伤未能降低纹状体中[3H]γ-羟基丁酸的结合。相反,尾状核-壳核(CPu)的 kainic 酸(KA)损伤导致约45%的结合丧失。对于海马体,隔海马通路的损伤并未改变受体密度,但海马体内注射 kainic 酸可大幅减弱(50%)[3H]GHB 的结合。这些结果表明,CPu 和背侧海马体中的γ-羟基丁酸受体主要位于内在神经元上,这些神经元可能参与γ-羟基丁酸在这些结构中所起作用的功能表达。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验