Suppr超能文献

大鼠脑中血管紧张素II受体结合的特异性

The specificity of angiotensin II receptor binding in rat brain.

作者信息

Cole F E, Blakesley H L, Graci K A, Frohlich E D, MacPhee A A

出版信息

Peptides. 1981 Winter;2(4):441-4. doi: 10.1016/s0196-9781(81)80102-7.

Abstract

125I-angiotensin II (125I-AII) binding was examined in the hypothalamic-thalamic-septal-midbrain (HTSM) region of HLA-Wistar rats in the presence of CNS-active agents. Angiotensin I, II, and III and saralasin competed for 125 I-AII binding, whereas structurally unrelated peptides such as arginine and lysine vasopressin, oxytocin, LHRH, TRH, bradykinin, and substance P did not. In contrast, ACTH and neurotensin exhibited a weak, dose-dependent competition for 125 I-AII binding. The relative potencies of AII, AI, neurotensin and ACTH were 100:1:0.1:0.05, respectively. Neurotensin and ACTH competition was not additive with AII suggesting interaction at shared binding sites. Most importantly, a wide variety of other CNS active agents such as methyldopa, naloxone, catecholamines, clondidine, and reserpine, failed to inhibit 125 I-AII binding, thus further defining the specificity of the CNS AII receptor.

摘要

在中枢神经系统活性药物存在的情况下,检测了HLA-威斯塔大鼠下丘脑-丘脑-隔区-中脑(HTSM)区域的125I-血管紧张素II(125I-AII)结合情况。血管紧张素I、II和III以及沙拉新竞争125I-AII结合,而结构不相关的肽如精氨酸和赖氨酸加压素、催产素、促黄体生成素释放激素、促甲状腺激素释放激素、缓激肽和P物质则不竞争。相反,促肾上腺皮质激素和神经降压素对125I-AII结合表现出微弱的剂量依赖性竞争。AII、AI、神经降压素和促肾上腺皮质激素的相对效力分别为100:1:0.1:0.05。神经降压素和促肾上腺皮质激素的竞争与AII不具有加和性,提示在共同结合位点存在相互作用。最重要的是,多种其他中枢神经系统活性药物如甲基多巴、纳洛酮、儿茶酚胺、可乐定和利血平未能抑制125I-AII结合,从而进一步明确了中枢神经系统AII受体的特异性。

相似文献

5
Distribution of angiotensin II receptor subtypes in rat brain nuclei.
Neurosci Lett. 1991 Oct 28;132(1):11-5. doi: 10.1016/0304-3940(91)90420-x.

引用本文的文献

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验