Iversen Leslie
Department of Pharmacology, University of Oxford, Mansfield Road, Oxford OX13QT, UK.
Biochem Pharmacol. 2004 Oct 15;68(8):1537-40. doi: 10.1016/j.bcp.2004.06.039.
Following the recognition of GABA as an inhibitory neurotransmitter, the discovery of high affinity GABA uptake, and the characterisation of GABA receptors great progress has been made in developing GABA pharmacology. Tiagabide, the first marketed GABA uptake inhibitor may be followed by new and more selective uptake inhibitors. Knowledge of the molecular pharmacology of GABA-A receptors, both synaptic and non-synaptic, may lead to improved anti-anxiety/anticonvulsant agents devoid of the sedative and dependence liabilities of earlier compounds and new hypnotics. Gaboxadol (THIP) is an example of a novel hypnotic that acts on GABA-A receptors by a non-benzodiazepine mechanism. Exploiting neurosteroid interactions with GABAergic mechanisms also holds much future promise.
在认识到γ-氨基丁酸(GABA)是一种抑制性神经递质、发现高亲和力GABA摄取以及对GABA受体进行表征之后,GABA药理学的发展取得了巨大进展。首个上市的GABA摄取抑制剂替加宾之后可能会出现新的、更具选择性的摄取抑制剂。对突触和非突触GABA-A受体分子药理学的了解,可能会带来改良的抗焦虑/抗惊厥药物,这些药物没有早期化合物的镇静和依赖性问题,还会带来新型催眠药。加波沙朵(THIP)是一种新型催眠药的例子,它通过非苯二氮䓬机制作用于GABA-A受体。利用神经甾体与GABA能机制的相互作用也具有很大的前景。