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3H-丙咪嗪和3H-去甲丙咪嗪在脑内的体内分布的放射自显影分析:与体外结合模式的比较。

Autoradiographic analysis of the in vivo distribution of 3H-imipramine and 3H-desipramine in brain: comparison to in vitro binding patterns.

作者信息

Duncan G E, Paul I A, Fassberg J B, Powell K R, Stumpf W E, Breese G R

机构信息

Department of Cell Biology and Anatomy, School of Medicine, University of North Carolina, Chapel Hill 27599.

出版信息

Pharmacol Biochem Behav. 1991 Mar;38(3):621-31. doi: 10.1016/0091-3057(91)90024-v.

Abstract

Using high resolution autoradiographic techniques, the distribution of radioactivity in forebrain and brainstem was assessed after IV injection of 3H-impramine or 3H-desipramine. Results were compared with regional binding of the drugs to brain sections in vitro. Similar topographic binding of 3H-imipramine and 3H-desipramine was observed in vitro among brain regions, except in the paraventricular nucleus of the hypothalamus and locus coeruleus, where binding was greater for 3H-desipramine. For both 3H-desipramine and 3H-imipramine, some brain regions that exhibited high binding in vitro also showed high accumulation after in vivo injection. However, certain regions that contained high densities of binding sites for the antidepressant drugs as measured by in vitro binding showed very low accumulation of radioactivity after in vivo treatment. Such regions included the dentate gyrus of the hippocampus, layer 1 of piriform cortex, caudate-putamen, pontine and midbrain central gray, and cerebellar granular layer. Compared to in vitro binding of the drugs, the distribution of imipramine and desipramine in vivo appears more anatomically selective. For imipramine, primary sites of action in vivo, as indicated by the topographic distribution in brain, appear to be the locus coeruleus, hippocampus, lateral septal nucleus, and amygdala. For desipramine, the greatest accumulation in vivo was found in the locus coeruleus, paraventricular nucleus of the hypothalamus, and anterior thalamic nuclei.

摘要

运用高分辨率放射自显影技术,在静脉注射3H-丙咪嗪或3H-去甲丙咪嗪后,评估前脑和脑干中的放射性分布。将结果与药物在体外与脑切片的区域结合情况进行比较。在体外,除了下丘脑室旁核和蓝斑中3H-去甲丙咪嗪的结合更强外,3H-丙咪嗪和3H-去甲丙咪嗪在脑区中的拓扑结合情况相似。对于3H-去甲丙咪嗪和3H-丙咪嗪而言,一些在体外表现出高结合的脑区在体内注射后也显示出高蓄积。然而,通过体外结合测定的含有抗抑郁药高密度结合位点的某些区域在体内处理后显示出非常低的放射性蓄积。这些区域包括海马齿状回、梨状皮质第1层、尾状核-壳核、脑桥和中脑中央灰质以及小脑颗粒层。与药物的体外结合相比,丙咪嗪和去甲丙咪嗪在体内的分布在解剖学上似乎更具选择性。对于丙咪嗪,如脑中的拓扑分布所示,体内的主要作用部位似乎是蓝斑、海马、外侧隔核和杏仁核。对于去甲丙咪嗪,体内最大蓄积量出现在蓝斑、下丘脑室旁核和丘脑前核。

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