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Neuroactive steroids reduce neuronal excitability by selectively enhancing tonic inhibition mediated by δ subunit-containing GABAA receptors

机译:具有神经活性的类固醇通过选择性增强含δ亚基的GABAA受体介导的强直抑制作用来降低神经元兴奋性

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摘要

Neuroactive steroids are potent modulators of γ-aminobutyric acid type A receptors (GABAARs), and their behavioral effects are generally viewed in terms of altered inhibitory synaptic transmission. Here we report that, at concentrations known to occur in vivo, neuroactive steroids specifically enhance a tonic inhibitory conductance in central neurons that is mediated by extrasynaptic δ subunit-containing GABAARs. The neurosteroid-induced augmentation of this tonic conductance decreases neuronal excitability. Fluctuations in the circulating concentrations of endogenous neuroactive steroids have been implicated in the genesis of premenstrual syndrome, postpartum depression, and other anxiety disorders. Recognition that δ subunit-containing GABAARs responsible for a tonic conductance are a preferential target for neuroactive steroids may lead to novel pharmacological approaches for the treatment of these common conditions.
机译:具有神经活性的类固醇是γ-氨基丁酸A型受体(GABAAR)的有效调节剂,通常从抑制突触传递的角度来观察其行为作用。在这里,我们报告说,在体内已知的浓度下,神经活性类固醇可特异性增强中枢神经元的强直性抑制传导,该传导性是由突触外δ亚基的GABAAR介导的。神经类固醇诱导的这种强直性传导的增加降低了神经元的兴奋性。内源性神经活性类固醇循环浓度的波动与经前综合症,产后抑郁症和其他焦虑症的发生有关。认识到负责补药传导的含δ亚基的GABAAR是神经活性类固醇的优先靶标,可能会导致治疗这些常见病症的新药理学方法。

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