Department of Anesthesiology (S.R.P., A.L.G., J.H.S., G.A.) and the Taylor Family Institute for Innovative Psychiatric Research (J.H.S., G.A.), Washington University School of Medicine, St. Louis, Missouri.
Department of Anesthesiology (S.R.P., A.L.G., J.H.S., G.A.) and the Taylor Family Institute for Innovative Psychiatric Research (J.H.S., G.A.), Washington University School of Medicine, St. Louis, Missouri
Mol Pharmacol. 2022 Feb;101(2):68-77. doi: 10.1124/molpharm.121.000385. Epub 2021 Dec 1.
The GABA receptor is inhibited by the endogenous sulfated steroids pregnenolone sulfate (PS) and dehydroepiandrosterone sulfate (DHEAS). It has been proposed in previous work that these steroids act by enhancing desensitization of the receptor. Here, we have investigated the modulatory effects of the steroids on the human 132L GABA receptor. Using electrophysiology and quantitative model-based data analysis, we show that exposure to the steroid promotes occupancy of a nonconducting state that retains high affinity to the transmitter but whose properties differ from those of the classic, transmitter-induced desensitized state. From the analysis of the inhibitory actions of two combined steroids, we infer that PS and DHEAS act through shared or overlapping binding sites. SIGNIFICANCE STATEMENT: Previous work has proposed that sulfated neurosteroids inhibit the GABA receptor by enhancing the rate of entry into the desensitized state. This study shows that the inhibitory steroids pregnenolone sulfate and dehydroepiandrosterone sulfate act through a common interaction site by stabilizing a distinct nonconducting state.
γ-氨基丁酸(GABA)受体受到内源性硫酸甾体(如孕烯醇酮硫酸盐和脱氢表雄酮硫酸盐)的抑制。先前的研究提出,这些甾体通过增强受体脱敏来发挥作用。在这里,我们研究了甾体对人 132L GABA 受体的调节作用。通过电生理学和定量基于模型的数据分析,我们表明,暴露于甾体会促进非传导状态的占据,这种状态保持对递质的高亲和力,但性质与经典的、递质诱导的脱敏状态不同。从对两种组合甾体的抑制作用的分析中,我们推断孕烯醇酮硫酸盐和脱氢表雄酮硫酸盐通过共享或重叠的结合位点起作用。
先前的工作提出,硫酸神经甾体通过增强进入脱敏状态的速率来抑制 GABA 受体。这项研究表明,抑制性甾体孕烯醇酮硫酸盐和脱氢表雄酮硫酸盐通过稳定一个独特的非传导状态,通过共同的相互作用位点起作用。