首页> 外文期刊>Frontiers in Systems Neuroscience >Behavioral Sensitization to the Disinhibition Effect of Ethanol Requires the Dopamine/Ecdysone Receptor in Drosophila
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Behavioral Sensitization to the Disinhibition Effect of Ethanol Requires the Dopamine/Ecdysone Receptor in Drosophila

机译:对乙醇的抑制作用的行为敏化需要果蝇中的多巴胺/蜕皮激素受体

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Male flies under the influence of ethanol display disinhibited courtship, which is augmented with repeated ethanol exposures. We have previously shown that dopamine is important for this type of ethanol-induced behavioral sensitization but the underlying mechanism is unknown. Here we report that DopEcR, an insect G-protein coupled receptor that binds to dopamine and steroid hormone ecdysone, is a major receptor mediating courtship sensitization. Upon daily ethanol administration, dumb and damb mutant males defective in D1 (dDA1/DopR1) and D5 (DAMB/DopR2) dopamine receptors, respectively, showed normal courtship sensitization; however, the DopEcR-deficient der males exhibited greatly diminished sensitization. der mutant males nevertheless developed normal tolerance to the sedative effect of ethanol, indicating a selective function of DopEcR in chronic ethanol-associated behavioral plasticity. DopEcR plays a physiological role in behavioral sensitization since courtship sensitization in der males was reinstated when DopEcR expression was induced during adulthood but not during development. When examined for the DopEcR’s functional site, the der mutant’s sensitization phenotype was fully rescued by restored DopEcR expression in the mushroom body (MB) αβ and γ neurons. Consistently, we observed DopEcR immunoreactivity in the MB calyx and lobes in the wild-type Canton-S brain, which was barely detectable in the der brain. Behavioral sensitization to the locomotor-stimulant effect has been serving as a model for ethanol abuse and addiction. This is the first report elucidating the mechanism underlying behavioral sensitization to another stimulant effect of ethanol.
机译:雄性苍蝇在乙醇的影响下表现出不拘一格的求爱欲,而这种行为会因反复暴露于乙醇而增加。先前我们已经表明,多巴胺对于这种类型的乙醇诱导的行为致敏作用很重要,但是其潜在机制尚不清楚。在这里,我们报道DopEcR,一种昆虫G蛋白偶联受体,与多巴胺和类固醇激素蜕皮激素结合,是介导求爱致敏作用的主要受体。每天服用乙醇后,分别在D1(dDA1 / DopR1)和D5(DAMB / DopR2)多巴胺受体中有缺陷的哑哑突变男性表现出正常的求爱敏锐性。然而,缺乏DopEcR的男性表现出大大降低的敏化作用。尽管如此,der突变男性对乙醇的镇静作用仍具有正常的耐受性,表明DopEcR在慢性乙醇相关的行为可塑性中具有选择性功能。 DopEcR在行为敏化中起着生理作用,因为在成年期间而不是发育过程中诱导DopEcR表达时,der男性的求爱敏化得以恢复。当检查DopEcR的功能位点时,通过突变的蘑菇体(MB)αβ和γ神经元中的DopEcR表达恢复,der突变体的致敏表型得以完全挽救。一致地,我们在野生型Canton-S脑的MB花萼和叶中观察到DopEcR免疫反应性,而在der脑中几乎检测不到。对运动刺激作用的行为敏化已成为乙醇滥用和成瘾的模型。这是第一份阐明行为敏化对乙醇另一种刺激作用的潜在机制的报道。

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