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果蝇中的乙醇中毒:cAMP信号通路调控的遗传和药理学证据。

Ethanol intoxication in Drosophila: Genetic and pharmacological evidence for regulation by the cAMP signaling pathway.

作者信息

Moore M S, DeZazzo J, Luk A Y, Tully T, Singh C M, Heberlein U

机构信息

Gallo Center and Department of Neurology, University of California, San Francisco, 94110, USA.

出版信息

Cell. 1998 Jun 12;93(6):997-1007. doi: 10.1016/s0092-8674(00)81205-2.

Abstract

Upon exposure to ethanol, Drosophila display behaviors that are similar to ethanol intoxication in rodents and humans. Using an inebriometer to measure ethanol-induced loss of postural control, we identified cheapdate, a mutant with enhanced sensitivity to ethanol. Genetic and molecular analyses revealed that cheapdate is an allele of the memory mutant amnesiac. amnesiac has been postulated to encode a neuropeptide that activates the cAMP pathway. Consistent with this, we find that enhanced ethanol sensitivity of cheapdate can be reversed by treatment with agents that increase cAMP levels or PKA activity. Conversely, genetic or pharmacological reduction in PKA activity results in increased sensitivity to ethanol. Taken together, our results provide functional evidence for the involvement of the cAMP signal transduction pathway in the behavioral response to intoxicating levels of ethanol.

摘要

暴露于乙醇时,果蝇会表现出与啮齿动物和人类乙醇中毒相似的行为。我们使用酒精测量仪来测量乙醇诱导的姿势控制丧失,鉴定出了cheapdate,这是一种对乙醇敏感性增强的突变体。遗传和分子分析表明,cheapdate是记忆突变体失忆症(amnesiac)的一个等位基因。据推测,失忆症编码一种激活cAMP途径的神经肽。与此一致的是,我们发现用增加cAMP水平或PKA活性的试剂处理可以逆转cheapdate对乙醇的增强敏感性。相反,PKA活性的遗传或药理学降低会导致对乙醇的敏感性增加。综上所述,我们的结果为cAMP信号转导途径参与对中毒水平乙醇的行为反应提供了功能证据。

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