Department of Pediatrics, Medical College of Wisconsin, Milwaukee, WI 53226, USA.
Psychoneuroendocrinology. 2009 Dec;34 Suppl 1:S67-73. doi: 10.1016/j.psyneuen.2009.08.010.
alphabetadelta-Containing GABA(A) receptors are (1) localized to extra- and perisynaptic membranes, (2) exhibit a high sensitivity to GABA, (3) show little desensitization, and (4) are believed to be one of the primary mediators of tonic inhibition in the central nervous system. This type of signaling appears to play a key role in controlling cell excitability. This review article briefly summarizes recent knowledge on tonic GABA-mediated inhibition. We will also consider the mechanism of action of many clinically important drugs such as anxiolytics, anticonvulsants, and sedative/hypnotics and their effects on delta-containing GABA receptor activation. We will conclude that alphabetadelta-containing GABA(A) receptors exhibit a relatively low efficacy that can be potentiated by endogenous modulators and anxiolytic agents. This scenario enables these particular GABA receptor combinations, upon neurosteroid exposure for example, to impart a profound effect on excitability in the central nervous system.
含阿尔法德尔塔的 GABA(A) 受体 (1) 定位于突触外和突触周围膜,(2) 对 GABA 具有高灵敏度,(3) 几乎没有脱敏作用,(4) 被认为是中枢神经系统中紧张性抑制的主要介质之一。这种信号传递方式似乎在控制细胞兴奋性方面起着关键作用。本文简要总结了最近关于紧张性 GABA 介导抑制的知识。我们还将考虑许多临床重要药物的作用机制,如抗焦虑药、抗惊厥药和镇静/催眠药,以及它们对含德尔塔 GABA 受体激活的影响。我们得出的结论是,含阿尔法德尔塔的 GABA(A) 受体的效能相对较低,可被内源性调节剂和抗焦虑药增强。这种情况使这些特定的 GABA 受体组合,例如在神经甾体暴露的情况下,对中枢神经系统的兴奋性产生深远的影响。