Γ-氨基丁酸A型受体 GABAA receptor
![GABAA 受体结构:上图: GABAA受体嵌入细胞膜的侧视图,标记有巴比妥类药物,乙醇和吸入性麻醉剂的位点。下图:视角在细胞膜外的受体俯视图,标记有GABAA受体亚基的名字,以及GABA和苯二氮䓬类药物的位点[1]](/uploads/202501/14/GABAAreceptor3642.jpg)


GABAA受体(又称作γ-氨基丁酸A型受体)是一种离子型受体,而且是一类配体门控型离子信道。此信道的内源性配体是一种被称为GABA的神经递质。GABA是中枢神经系统里的一种主要的递质,虽然GABA在神经递质的释放过程中产生的是抑制性效应,但GABA本身并非一种抑制性而是一种刺激性递质,因为GABA激活GABA受体的开放。在GABAA受体被激活后,可以选择性的让Cl通过,引起神经元的超极化。这种超极化引起了神经信号传递抑制,因为降低了动作电位产生的成功率GABAA,在正常条件下产生的抑制性突触后电位的翻转电位是-75 mV,高于GABAB受体的-100 mV。
![Structure of the nicotinic acetylcholine receptor (nAchR: PDB: 2BG9) which is very similar to the GABAA receptor.[1][2][3] Top: side view of the nAchR imbedded in a cell membrane. Bottom: view of the receptor from the extracellular face of the membrane. The subunits are labeled according to the GABAA nomenclature and the approximate locations of the GABA and benzodiazepine (BZ) binding sites are noted (between the α- and β-subunits and between the α- and γ-subunits respectively).](/uploads/202501/14/NAchR_2BG93642.png)

![Schematic diagram of a GABAA receptor protein ((α1)2(β2)2(γ2)) which illustrates the five combined subunits that form the protein, the chloride (Cl−) ion channel pore, the two GABA active binding sites at the α1 and β2 interfaces, and the benzodiazepine (BDZ) allosteric binding site[1]](/uploads/202501/14/GABAA-receptor-protein-example3643.png)