Mortensen Martin, Bright Damian P, Fagotti Juliane, Dorovykh Valentina, Cerna Barbora, Smart Trevor G
University College London, Dept Neuroscience, Physiology & Pharmacology, Gower Street, London WC1E 6BT, United Kingdom.
University College London, Dept Neuroscience, Physiology & Pharmacology, Gower Street, London WC1E 6BT, United Kingdom.
Neuroscience. 2025 Jul 10;578:6-24. doi: 10.1016/j.neuroscience.2024.06.002. Epub 2024 Jun 7.
Brain inhibition is a vital process for controlling and sculpting the excitability of the central nervous system in healthy individuals. This level of control is provided over several timescales and involves the neurotransmitter GABA acting at inhibitory synapses to: rapidly inhibit neurons by activating the GABA receptor; over a slower timescale, to tonically activate extrasynaptic GABA receptors to provide a low level of background inhibition; and finally, to activate G-protein coupled GABA receptors to control transmitter release by inhibiting presynaptic Ca channels whilst providing postsynaptic inhibition via K channel activation. From this plethora of roles for GABA and its receptors, the GABA receptor isoform is of major interest due to its dynamic functional plasticity, which in part, is due to being targeted by modulatory brain neurosteroids derived from sex and stress hormones. This family of neurosteroids can, depending on their structure, potentiate, activate and also inhibit the activity of GABA receptors to affect brain inhibition. This review tracks the methods that have been deployed in probing GABA receptors, and charts the sterling efforts made by several groups to locate the key neurosteroid binding sites that affect these important receptors. Increasing our knowledge of these binding sites will greatly facilitate our understanding of the physiological roles of neurosteroids and will help to advance their use as novel therapeutics to combat debilitating brain diseases.
在健康个体中,大脑抑制是控制和塑造中枢神经系统兴奋性的重要过程。这种控制水平在多个时间尺度上发挥作用,涉及神经递质γ-氨基丁酸(GABA)作用于抑制性突触,以:通过激活GABA受体快速抑制神经元;在较慢的时间尺度上,持续激活突触外GABA受体以提供低水平的背景抑制;最后,激活G蛋白偶联GABA受体,通过抑制突触前钙通道来控制神经递质释放,同时通过激活钾通道提供突触后抑制。鉴于GABA及其受体具有如此众多的功能,GABA受体亚型因其动态功能可塑性而备受关注,部分原因是它受到源自性和应激激素的调节性脑甾体的作用。根据其结构,这类神经甾体可以增强、激活并抑制GABA受体的活性,从而影响大脑抑制。这篇综述追踪了用于探究GABA受体的方法,并梳理了多个研究团队为定位影响这些重要受体的关键神经甾体结合位点所做出的卓越努力。增加我们对这些结合位点的了解将极大地促进我们对神经甾体生理作用的理解,并有助于推动其作为新型治疗药物用于对抗使人衰弱的脑部疾病。