Akk Gustav, Shu Hong-Jin, Wang Cunde, Steinbach Joe Henry, Zorumski Charles F, Covey Douglas F, Mennerick Steven
Department of Anesthesiology, Washington University, St. Louis, Missouri 63110, USA.
J Neurosci. 2005 Dec 14;25(50):11605-13. doi: 10.1523/JNEUROSCI.4173-05.2005.
GABAA receptors are a pivotal inhibitory influence in the nervous system, and modulators of the GABAA receptor are important anesthetics, sedatives, anticonvulsants, and anxiolytics. Current views of receptor modulation suggest that many exogenous drugs access and bind to an extracellular receptor domain. Using novel synthetic steroid analogs, we examined the access route for neuroactive steroids, potent GABAA receptor modulators also produced endogenously. Tight-seal recordings, in which direct aqueous drug access to receptor was prevented, demonstrated that steroids can reach the receptor either through plasma membrane lateral diffusion or through intracellular routes. A fluorescent neuroactive steroid accumulated intracellularly, but recordings from excised patches indicated that the intracellular reservoir is not necessary for receptor modulation, although it can apparently equilibrate with the plasma membrane within seconds. A membrane impermeant neuroactive steroid modulated receptor activity only when applied to the inner membrane leaflet, demonstrating that the steroid does not access an extracellular modulatory site. Thus, neuroactive steroids do not require direct aqueous access to the receptor, and membrane accumulation is required for receptor modulation.
GABAA受体是神经系统中关键的抑制性影响因素,GABAA受体调节剂是重要的麻醉剂、镇静剂、抗惊厥药和抗焦虑药。目前关于受体调节的观点认为,许多外源性药物进入并结合到细胞外受体结构域。我们使用新型合成类固醇类似物,研究了神经活性类固醇的进入途径,神经活性类固醇也是内源性产生的强效GABAA受体调节剂。在紧密密封记录中,直接阻止药物通过水相进入受体,结果表明类固醇可以通过质膜侧向扩散或通过细胞内途径到达受体。一种荧光神经活性类固醇在细胞内积累,但从切除的膜片上记录表明,细胞内储存库对于受体调节并非必需,尽管它显然可以在几秒钟内与质膜达到平衡。一种膜不透性神经活性类固醇只有在应用于内膜小叶时才调节受体活性,这表明该类固醇无法进入细胞外调节位点。因此,神经活性类固醇不需要通过水相直接进入受体,受体调节需要膜积累。