受体
γ-氨基丁酸受体
神经科学
功能多样性
药理学
计算生物学
功能(生物学)
生物
离子通道
细胞生物学
生物化学
生态学
作者
Han Chow Chua,Mary Chebib
标识
DOI:10.1016/bs.apha.2017.03.003
摘要
GABAA receptors (GABAARs) are a class of ligand-gated ion channels with high physiological and therapeutic significance. In the brain, these pentameric receptors occur with diverse subunit composition, which confers highly complex pharmacology to this receptor class. An impressive range of clinically used therapeutics are known to bind to distinct sites found on GABAARs to modulate receptor function. Numerous experimental approaches have been used over the years to elucidate the binding sites of these drugs, but unequivocal identification is challenging due to subtype- and ligand-dependent pharmacology. Here, we review the current structural and pharmacological understanding of GABAARs, besides highlighting recent evidence which has revealed greater complexity than previously anticipated.
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