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来自(低情绪)罗马高回避型和(高情绪)低回避型大鼠脑区的γ-氨基丁酸A(GABA(A))受体复合物的药理学特性

Pharmacological properties of the GABA(A) receptor complex from brain regions of (hypoemotional) Roman high- and (hyperemotional) low-avoidance rats.

作者信息

Bentareha R, Araujo F, Ruano D, Driscoll P, Escorihuela R M, Tobeña A, Fernández-Teruel A, Vitorica J

机构信息

Departamento Bioquimica, Bromatologia y Toxicologia, Facultad de Farmacia, Universidad de Sevilla, Spain.

出版信息

Eur J Pharmacol. 1998 Jul 31;354(1):91-7. doi: 10.1016/s0014-2999(98)00428-2.

Abstract

The pharmacological properties of benzodiazepine binding sites of the gamma-aminobutyric acid (GABA)A receptor complex from cortical, hippocampal and cerebellar membranes of Roman high-avoidance (RHA/Verh) and Roman low-avoidance (RLH/Verh) rats were investigated. No major differences between the two lines were found in the binding parameters of [3H]flunitrazepam (a non-selective agonist). [3 H]zolpidem (a Type I selective agonist) or [3 H]ethyl 8-azido-6-dihydro-5-methyl-6-oxo-4H-imidazol[1,5-a]-[1,4]benzodiazepine- 3-carboxylate (Ro15-4513) (a partial inverse agonist). Neither the Kd values nor the Bmax for these ligands differed between RHA/Verh and RLA/Verh rats in any of the brain regions studied. As a result, the proportion of Type I binding sites in cortical and hippocampal membranes of RHA/Verh and RLA/Verh rats or the 'diazepam-sensitive' and the 'diazepam-insensitive' binding sites in cerebellar membranes, calculated from the [3H]flunitrazepam and [3H]zolpidem maximal binding sites or from [3H]Ro15-4513 binding (in the absence or in presence of diazepam), respectively, was also similar. Furthermore, there were no differences between the two rat lines in the allosteric interactions between GABA and the benzodiazepine binding sites (labeled with [3H]flunitrazepam) in all three areas tested or the Type I binding sites (labeled with [3H]zolpidem) in the hippocampus. In contrast, RLA/Verh rats showed a significant reduction in the allosteric interactions between GABA and [3H]zolpidem binding sites in the cortex. As a whole, these results indicate the absence of generalized between-line differences in the GABA(A) receptor complex showing, at the same time, the existence of some specific differences in allosterism within the GABA(A) complex. These differences may contribute to the divergent emotional responses which characterize the RHA/Verh and RLA/Verh rat lines.

摘要

研究了来自罗马高回避型(RHA/Verh)和罗马低回避型(RLH/Verh)大鼠皮质、海马和小脑膜的γ-氨基丁酸(GABA)A受体复合物苯二氮䓬结合位点的药理学特性。在[3H]氟硝西泮(一种非选择性激动剂)、[3H]唑吡坦(一种I型选择性激动剂)或[3H]乙基8-叠氮基-6-二氢-5-甲基-6-氧代-4H-咪唑并[1,5-a][1,4]苯二氮䓬-3-羧酸酯(Ro15-4513)(一种部分反向激动剂)的结合参数方面,未发现两品系之间存在主要差异。在所研究的任何脑区中,这些配体的Kd值和Bmax在RHA/Verh和RLA/Verh大鼠之间均无差异。因此,根据[3H]氟硝西泮和[3H]唑吡坦的最大结合位点或分别根据[3H]Ro15-4513结合(在有无地西泮的情况下)计算得出的RHA/Verh和RLA/Verh大鼠皮质和海马膜中I型结合位点的比例,或小脑膜中“地西泮敏感”和“地西泮不敏感”结合位点的比例也相似。此外,在所有三个测试区域中,GABA与苯二氮䓬结合位点(用[3H]氟硝西泮标记)之间的变构相互作用,或海马中I型结合位点(用[3H]唑吡坦标记)之间的变构相互作用,在两个大鼠品系之间没有差异。相比之下,RLA/Verh大鼠在皮质中GABA与[3H]唑吡坦结合位点之间的变构相互作用显著降低。总体而言,这些结果表明GABA(A)受体复合物中不存在品系间的普遍差异,同时也表明GABA(A)复合物内部变构存在一些特定差异。这些差异可能导致RHA/Verh和RLA/Verh大鼠品系具有不同的情绪反应特征。

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