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作为新型假定抗焦虑药TVX Q 7821靶点的高亲和力5-羟色胺受体亚型的放射自显影鉴定及拓扑分析

Autoradiographic identification and topographical analyses of high affinity serotonin receptor subtypes as a target for the novel putative anxiolytic TVX Q 7821.

作者信息

Glaser T, Rath M, Traber J, Zilles K, Schleicher A

出版信息

Brain Res. 1985 Dec 9;358(1-2):129-36. doi: 10.1016/0006-8993(85)90956-4.

DOI:10.1016/0006-8993(85)90956-4
PMID:2866816
Abstract

TVX Q 7821 is a putative non-benzodiazepine anxiolytic which has a high affinity to 5-HT1 receptors. In this study some of the binding characteristics of the radiolabeled drug using rat brain cryostat sections and the autoradiographic localization of binding sites using the LKB-Ultrofilm technique have been investigated. Parallel experiments have been performed using [3H]serotonin ( [3H]5-HT). Both [3H]TVX Q 7821 and [3H]5-HT bound specifically and in a saturable manner to tissue sections, the Kd values being 6.8 and 3.7 nmol/l, respectively. Quantitative autoradiography using computer-assisted image analysis revealed a mean inhibition by TVX Q 7821 of [3H]5-HT binding of 56% in many brain areas. The inhibition ranged from 80% in the hippocampus and entorhinal area to practically none in the substantia nigra and the dorsal subiculum. Color coded autoradiograms obtained either with [3H]5-HT or [3H]TVX Q 7821 showed a nearly identical pattern of labeling with high receptor densities in the hippocampus, the entorhinal area, the septum, the interpeduncular nucleus and the dorsal raphe. However, in some brain areas striking differences in the intensity of labeling were found. [3H]5-HT but not [3H]TVX Q 7821 bound strongly in the substantia nigra, the dorsal subiculum and the globus pallidus. It is proposed that TVX Q 7821 binds to a subtype of 5-HT1 receptor (the so-called 5-HT1A sites as recently proposed). Thus, the putative anxiolytic TVX Q 7821 may provide a means for the study of the functional role of 5-HT1 receptors.

摘要

TVX Q 7821是一种假定的非苯二氮䓬类抗焦虑药,对5-羟色胺(5-HT)1受体具有高亲和力。在本研究中,使用大鼠脑恒冷箱切片对放射性标记药物的一些结合特性进行了研究,并使用LKB-Ultrofilm技术对结合位点进行了放射自显影定位。同时进行了使用[3H]5-羟色胺([3H]5-HT)的平行实验。[3H]TVX Q 7821和[3H]5-HT均以特异性和可饱和的方式与组织切片结合,解离常数(Kd)值分别为6.8和3.7nmol/L。使用计算机辅助图像分析的定量放射自显影显示,在许多脑区TVX Q 7821对[3H]5-HT结合的平均抑制率为56%。抑制率范围从海马和内嗅区的80%到黑质和背侧下托几乎为零。用[3H]5-HT或[3H]TVX Q 7821获得的彩色编码放射自显影片显示,在海马、内嗅区、隔区、脚间核和中缝背核中标记模式几乎相同,受体密度较高。然而,在一些脑区发现标记强度存在显著差异。[3H]5-HT而非[3H]TVX Q 7821在黑质、背侧下托和苍白球中强烈结合。有人提出TVX Q 7821与5-HT1受体的一个亚型结合(最近提出的所谓5-HT1A位点)。因此,假定的抗焦虑药TVX Q 7821可能为研究5-HT1受体的功能作用提供一种手段。

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