Department of Neurosciences, School of Medical Sciences, Universiti Sains Malaysia, Kampus Kesihatan, 16150, Kubang Kerian, Kelantan, Malaysia.
J Mol Neurosci. 2019 Feb;67(2):343-351. doi: 10.1007/s12031-018-1246-4. Epub 2019 Jan 3.
GABA receptors are the major inhibitory neurotransmitter receptor in the human brain. The receptors are assembled from combination of protein subunits in pentameric complex which may consist of α1-6, β1-3, γ1-3, ρ1-3, δ, ε, θ, or π subunits. There are a theoretical > 150,000 possible assemblies and arrangements of GABA subunits, although only a few combinations have been found in human with the most dominant consists of 2α1, 2β2, and 1γ2 in a counterclockwise arrangement as seen from the synaptic cleft. The receptors also possess binding sites for various unrelated substances including benzodiazepines, barbiturates, and anesthetics. The α5-containing GABARs only make up ≤ 5% of the entire receptor population, but up to 25% of the receptor subtype is located in the crucial learning and memory-associated area of the brain-the hippocampus, which has ignited myriads of hypotheses and theories in regard to its role. As well as exhibiting synaptic phasic inhibition, the α5-containing receptors are also extrasynaptic and mediate tonic inhibition with continuously occurring smaller amplitude. Studies on negative-allosteric modulators for reducing this tonic inhibition have been shown to enhance learning and memory in neurological disorders such as schizophrenia, Down syndrome, and autism with a possible alternative benzodiazepine binding site. Therefore, a few α5 subunit-specific compounds have been developed to address these pharmacological needs. With its small population, the α5-containing receptors could be the key and also the answer for many untreated cognitive dysfunctions and disorders.
GABA 受体是人类大脑中主要的抑制性神经递质受体。这些受体由五聚体复合物中的蛋白质亚基组合而成,五聚体复合物可能由 α1-6、β1-3、γ1-3、ρ1-3、δ、ε、θ 或 π 亚基组成。理论上 GABA 亚基的组合和排列方式有>150000 种,尽管在人类中只发现了少数几种组合,其中最主要的组合由 2α1、2β2 和 1γ2 组成,从突触裂隙看呈逆时针排列。这些受体还具有结合各种不相关物质的结合位点,包括苯二氮䓬类、巴比妥类和麻醉剂。含 α5 的 GABAR 仅占整个受体群体的≤5%,但多达 25%的受体亚型位于大脑中与学习和记忆相关的关键区域——海马体,这引发了无数关于其作用的假说和理论。除了表现出突触相抑制外,含 α5 的受体还具有突触外抑制作用,并通过持续发生的较小幅度来介导紧张性抑制。研究表明,减少这种紧张性抑制的负变构调节剂可增强神经精神障碍(如精神分裂症、唐氏综合征和自闭症)中的学习和记忆,可能存在替代的苯二氮䓬结合位点。因此,已经开发了几种针对特定 α5 亚基的化合物来满足这些药理学需求。由于其数量较少,含 α5 的受体可能是许多未经治疗的认知功能障碍和疾病的关键,也是答案。