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GABAA Receptors and the Diversity in their Structure and Pharmacology.
Chua, Han Chow; Chebib, Mary.
Afiliação
  • Chua HC; Faculty of Pharmacy, The University of Sydney, Sydney, NSW, Australia.
  • Chebib M; Faculty of Pharmacy, The University of Sydney, Sydney, NSW, Australia. Electronic address: mary.collins@sydney.edu.au.
Adv Pharmacol ; 79: 1-34, 2017.
Article em En | MEDLINE | ID: mdl-28528665
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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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Receptores de GABA-A Limite: Animals / Humans Idioma: En Revista: Adv Pharmacol Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Austrália

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Receptores de GABA-A Limite: Animals / Humans Idioma: En Revista: Adv Pharmacol Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Austrália