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3β-Methyl-Neurosteroid Analogs Are Preferential Positive Allosteric Modulators and Direct Activators of Extrasynaptic δ-Subunit γ-Aminobutyric Acid Type A Receptors in the Hippocampus Dentate Gyrus Subfield

Neurosteroids are powerful modulators of γ-aminobutyric acid (GABA)-A receptors. Ganaxolone (3α-hydroxy-3β-methyl-5α-pregnan-20-one, GX) and synthetic analogs of the neurosteroid allopregnanolone (AP) are designed to treat epilepsy and related conditions. However, their precise mechanism of action i...

詳細記述

保存先:
書誌詳細
出版年:J Pharmacol Exp Ther
主要な著者: Chuang, Shu-Hui, Reddy, Doodipala Samba
フォーマット: Artigo
言語:Inglês
出版事項: The American Society for Pharmacology and Experimental Therapeutics 2018
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC5941194/
https://ncbi.nlm.nih.gov/pubmed/29602830
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1124/jpet.117.246660
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