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Glyoxalase (GLO1) inhibition or genetic overexpression does not alter ethanol’s locomotor effects: implications for GLO1 as a therapeutic target in alcohol use disorders

机译:乙二醛酶(GLO1)的抑制或基因过表达不会改变乙醇的运动效果:对GLO1作为酒精使用障碍的治疗靶标的意义

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摘要

BackgroundGlyoxalase 1 (>GLO1) is an enzyme that metabolizes methylglyoxal (>MG), which is a competitive partial agonist at GABAA receptors. Inhibition of GLO1 increases concentrations of MG in the brain and decreases binge-like ethanol drinking. The present study assessed whether inhibition of GLO1, or genetic over expression of Glo1, would also alter the locomotor effects of ethanol, which might explain reduced ethanol consumption following GLO1 inhibition. We used the prototypical GABAA receptor agonist muscimol as a positive control.
机译:背景乙二醛酶1(> GLO1 )是一种代谢甲基乙二醛(> MG )的酶,甲基乙二醛是GABAA受体的竞争性部分激动剂。抑制GLO1可增加大脑中MG的浓度,并减少狂饮般的乙醇饮酒。本研究评估了抑制GLO1或基因过量表达Glo1是否也会改变乙醇的运动效果,这可能解释了抑制GLO1后乙醇消耗减少的原因。我们使用原型GABAA受体激动剂麝香酚作为阳性对照。

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