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- W1993926377 abstract "The gamma-aminobutyric acid-A (GABAA) receptors is the target for the most widely prescribed sleep medicines. It is a ligand-gated ion channel, activated by the amino acid neurotransmitter GABA, which normally results in hyperpolarization of neurons leading to reduced action potential firing, and thereby a reduction in neuronal activity. It has a rich pharmacology with a number of separate modulator binding sites. The best studied of these is the benzodiazepine site. Modulation of GABAA receptor activity by benzodiazepines produces sedative, hypnotic, anxiolytic and anticonvulsant activities. Short half-life benzodiazepines such as triazolam have been particularly useful in treating insomnia, but concerns have been raised regarding tolerance potential and dependence liability of classical benzodiazepines, which has led to reduced prescribing of these agents. In recent years, the treatment of sleep disorders has moved towards the use of non-benzodiazepine sedative hypnotics. These agents act at the same site on the GABAA receptor, but feature less of the problems associated with classical benzodiazepines. Recent progress in our understanding of the diversity and pharmacology of GABAA receptor subtypes has provided a rational explanation for the efficacy of these compounds. Findings from preclinical studies reveal promising avenues for the design of better therapeutics in the near future." @default.
- W1993926377 created "2016-06-24" @default.
- W1993926377 creator A5055924518 @default.
- W1993926377 date "2004-01-01" @default.
- W1993926377 modified "2023-10-11" @default.
- W1993926377 title "The benzodiazepine site of the GABA receptor: an old target with new potential?" @default.
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- W1993926377 doi "https://doi.org/10.1016/s1389-9457(04)90002-0" @default.
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