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褪黑素结合位点在山羊脑中的体外放射自显影定位

In vitro autoradiographical localization of melatonin binding sites in the caprine brain.

作者信息

Deveson S, Howarth J A, Arendt J, Forsyth I A

机构信息

School of Biological Sciences, University of Surrey, Guildford, U.K.

出版信息

J Pineal Res. 1992 Aug;13(1):6-12. doi: 10.1111/j.1600-079x.1992.tb00048.x.

Abstract

The recent development of a specific 2-[125I]-iodo-melatonin ligand has led to the identification of 125I-melatonin binding sites in the brains of numerous mammalian species. The present study reports the localization of 125I-melatonin binding sites in the brain of the dairy goat. Six previously untreated female goats, aged 5-7 years, were culled under natural light between 0900 and 1100. Brains and pituitaries were immediately dissected out and frozen on dry ice. Both transverse and sagittal sections of frozen brain were cut 20 microns thick and thaw-mounted onto gelatin-coated slides. Three consecutive sections were cut at intervals throughout the brain, mounted onto three slides, labeled A, B, and C, and thusly treated: (A) incubated for 2 hr at room temperature in a 50 pM solution of 125I-melatonin; (B) incubated for 2 hr at room temperature in a 50 pM solution of 125I-melatonin plus 1 microM cold melatonin; (C) fixed in Clarke's fluid and stained with toluidine blue. After incubation, A (specific) and B (nonspecific) slides were washed three times in ice-cold Tris-HCl buffer (pH 7.7), air-dried, exposed to an X-ray film for 2 weeks at -20 degrees C, and then fixed and stained. Specific 125I-melatonin binding sites were found in the pars tuberalis (PT), the area of the suprachiasmatic nucleus (SCN), preoptic area (POA), fornix/mediolateral septal areas, hippocampus, and the cerebral cortex. 125I-melatonin did not bind in the hindbrain, midbrain, neurohypophysis, pars intermedia or pars distalis of the adenohypophysis, or the pineal.

摘要

一种特异性的2-[¹²⁵I]-碘褪黑素配体的最新研制成果,使得在众多哺乳动物的大脑中发现了¹²⁵I-褪黑素结合位点。本研究报告了¹²⁵I-褪黑素结合位点在奶山羊大脑中的定位情况。选取6只此前未接受过处理的5至7岁雌性山羊,于上午9点至11点在自然光下扑杀。立即取出大脑和垂体,在干冰上冷冻。将冷冻大脑切成20微米厚的横切片和矢状切片,解冻后贴附在涂有明胶的载玻片上。在整个大脑中每隔一定间隔切取连续的3个切片,贴附在3张载玻片上,分别标记为A、B和C,并进行如下处理:(A)在室温下于50 pM的¹²⁵I-褪黑素溶液中孵育2小时;(B)在室温下于50 pM的¹²⁵I-褪黑素溶液加1 μM冷褪黑素中孵育2小时;(C)用克拉克液固定并用甲苯胺蓝染色。孵育后,将A(特异性)和B(非特异性)载玻片在冰冷的Tris-HCl缓冲液(pH 7.7)中洗涤3次,空气干燥,在-20℃下与X射线胶片接触2周,然后固定并染色。在结节部(PT)、视交叉上核(SCN)区域、视前区(POA)、穹窿/内侧外侧隔区、海马体和大脑皮层中发现了特异性的¹²⁵I-褪黑素结合位点。¹²⁵I-褪黑素在后脑、中脑、神经垂体、腺垂体的中间部或远侧部以及松果体中未结合。

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