Neurosteroids represent a class of endogenous steroids that are synthesized in the brain, the adrenals and the gonads and have potent and selective effects on the gamma-aminobutyric acid type A (GABAA receptor). 3α-Hydroxy A-ring-reduced metabolites of progesterone, deoxycorticosterone and testosterone enhance the the Cl- flux through GABAA receptor conductance at nanomolar concentrations in a non-genomic (rapid and direct) manner. Studies on the GABAA receptors have shown that allopregnanolone (3α-OH-5α-pregnan-20-one), 5α-androstane- 3α,17α- diol (Adiol) and (3 5 3, 21-dihydroxypregnan-20-one (3α5αTHDOC) enhance the GABA mediated Cl- currents acting on a site (or sites) distinct from the GABA, benzodiazepine, barbiturate and picrotoxin binding sites. This modulation site (or sites) has a well-defined structure-activity relationship with a 3α-hydroxy and a 20-ketone configuration in the pregnane molecule required for agonist action. However, the neurosteroid pregnenolone sulfate (PS) is a non-competitive GABAA receptor antagonist and inhibits GABA-activated Cl- currents in an activationdependent manner. 3β-hydroxy A-ring reduced pregnane steroids are pregnenolone sulfate-like GABAA receptors antagonists and inhibit the GABAA receptor's function and its potentiation induced by their 3α-diasteromers in a non-competitive manner. The specificity of neurosteroid action on the GABAA receptor results from a variety of molecular mechanisms, including receptor subunit composition, receptor activation-deactivation, and steroid concentration. Here, we will review the GABAmodulatory actions of the neurosteroids. The molecular mechanisms underpinning the non-genomic effect of agonist and antagonist neurosteroids will be discussed with particular emphasis being given to the role of GABA A receptor isoforms. © 2008 Springer Netherlands.
CITATION STYLE
Wang, M. D., Rahman, M., Strömberg, J., Lundgren, P., Haage, D., Johansson, I. M., & Bückström, T. (2008). Neurosteroid: Molecular mechanisms of action on the GABAA receptor. In Neuroactive Steroids in Brain Function, Behavior and Neuropsychiatric Disorders: Novel Strategies for Research and Treatment (pp. 3–42). Springer Netherlands. https://doi.org/10.1007/978-1-4020-6854-6_1
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