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首页> 外文期刊>Brain structure & function >Mesoaeciimbens dopamine signaling alteration underlies behavioral transition from tolerance to sensitization to morphine rewarding properties during morphine withdrawal
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Mesoaeciimbens dopamine signaling alteration underlies behavioral transition from tolerance to sensitization to morphine rewarding properties during morphine withdrawal

机译:Mesoaeciimbens多巴胺信号转导基础是吗啡戒断期间从耐受性向敏化到吗啡奖励特性的行为转变

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Although the firing activity of dopamine (DA) neurons in the ventral tegmental area (VTA) and the behavioral response to morphine rewarding properties alter as opiate^ withdrawal, little is known about the dynamic changes in DA signal pathway from the VTA to the nucleus accumbens (NAc) during prolonged withdrawal, and whether the changes are indicative of vulnerability to relapse of drug abuse. Here we report that morphine spontaneously withdrawn (SW) rats are incapable of responding to small dose of morphine-induced conditioned place preference (CPP) from 24h-SW to 30d-SW, but recover response at 45d-SW. Interestingly, mesoaccum-bens DA signaling, including the firing of DA neurons in the VTA, contents of DA and its metabolic ratio, and the membrane level of dopamine Di receptor in the NAc elicited by morphine challenge, display a similar pattern of time-dependent changes during morphine withdrawal. Moreover, blockade of Di receptor abolishes this behavioral transition. In addition, a strong correlation was found between % change in CPP score and membrane Dt receptor level induced by morphine challenge. These results indicate a time-dependent behavioral switch from tolerance to sensitization during the prolonged withdrawal, which could offer a window for therapeutic intervention via manipulations of Dj receptors.
机译:尽管腹侧被盖区(VTA)的多巴胺(DA)神经元的放电活性和对吗啡奖励特性的行为反应会随着鸦片撤药而改变,但对从VTA到伏隔核的DA信号途径的动态变化知之甚少(NAc)期间,以及这些变化是否表明易受滥用药物复发的影响。在这里,我们报告吗啡自发撤回(SW)大鼠无法从24h-SW到30d-SW对小剂量吗啡诱导的条件性位置偏爱(CPP)做出反应,但在45d-SW时可以恢复反应。有趣的是,中膜-苯DA信号,包括VTA中DA神经元的放电,DA的含量及其代谢率以及吗啡激发引起的NAc中多巴胺Di受体的膜水平,表现出类似的时变模式吗啡戒断期间发生变化。而且,对Di受体的阻断消除了这种行为转变。此外,发现吗啡激发引起的CPP分数变化百分比与膜Dt受体水平之间存在很强的相关性。这些结果表明在长期戒断期间从耐受性到致敏性的时间依赖性行为转变,这可能为通过操纵Dj受体进行治疗干预提供了一个窗口。

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