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A prior history of binge-drinking increases sensitivity to the motivational valence of methamphetamine in female C57BL/6J mice

机译:暴饮的既往史增加了雌性C57BL / 6J小鼠对甲基苯丙胺动机价的敏感性

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摘要

Methamphetamine (MA) and alcohol use disorders exhibit a high degree of co-morbidity and sequential alcohol-MA mixing increases risk for co-abuse. Recently, we reported greater MA-conditioned reward in male C57BL/6J mice with a prior history of binge alcohol-drinking (14 days of 2-hour access to 5, 10, 20 and 40% alcohol). As female mice tend to binge-drink more alcohol than males and females tend to be more sensitive than males to the psychomotor-activating properties of MA, we first characterized the effects of binge-drinking upon MA-induced place-conditioning (four pairings of 0.25, 0.5, 1, 2, or 4 mg/kg IP) in females and then incorporated our prior data to analyze for sex differences in MA-conditioned reward. Prior binge-drinking history did not significantly affect locomotor hyperactivity or its sensitization in female mice. However, the dose-response function for place-conditioning was shifted to the left of water-drinking controls, indicating an increase in sensitivity to MA-conditioned reward. The examination of sex differences revealed no sex differences in alcohol intake, although females exhibited greater MA-induced locomotor stimulation than males, irrespective of their prior drinking history. No statistically significant sex difference was apparent for the potentiation of MA-conditioned reward produced by prior binge-drinking history. If relevant to humans, these data argue that both males and females with a prior binge-drinking history are similarly vulnerable to MA abuse and it remains to be determined whether or not the neural substrates underpinning this increased vulnerability reflect common or sex-specific adaptations in reward-related brain regions.
机译:甲基苯丙胺(MA)和酒精使用障碍表现出高度的合并症,并且连续的酒精-MA混合使用会增加共同滥用的风险。最近,我们报道了在有暴饮酒史的雄性C57BL / 6J小鼠中获得更高的MA条件奖励(14小时的2小时可获得5、10、20和40%的酒精)。由于雌性老鼠对男性的狂饮酒比雄性酒多,而雌性老鼠对MA的精神运动激活特性比雄性酒更敏感,因此,我们首先表征了暴饮酒对MA诱导的位置调节的影响(四对成对雌性,分别为0.25、0.5、1、2或4μmg/ kg IP),然后纳入我们的先前数据,以分析以MA为条件的奖励中的性别差异。先前的暴饮暴食史并未显着影响雌性小鼠运动过度活跃或其敏化作用。但是,用于场所调节的剂量反应功能被移至饮水控件的左侧,表明对通过MA调节的奖励的敏感性增加。性别差异的检查显示酒精摄入量无性别差异,尽管女性表现出比男性更大的MA诱导的运动刺激,无论其先前的饮酒史如何。由先前的暴饮暴食史产生的MA条件奖励的增强没有统计学上的显着性别差异。如果与人类相关,则这些数据认为,有暴饮史的男性和女性同样容易受到MA滥用的影响,尚需确定支撑这种增加的脆弱性的神经基质是否反映了人类的普遍适应或性别适应。奖励相关的大脑区域。

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