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首页> 外文期刊>International journal of developmental neuroscience: the official journal of the International Society for Developmental Neuroscience >Adult rat morphine exposure changes morphine preference, anxiety, and the brain expression of dopamine receptors in male offspring
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Adult rat morphine exposure changes morphine preference, anxiety, and the brain expression of dopamine receptors in male offspring

机译:成年大鼠吗啡暴露会改变吗啡偏好,焦虑和男性后代多巴胺受体的脑表达

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Addiction to drugs, including opioids is the result of an interplay between environmental and genetic factors. It has been shown that the progeny of addict people is at higher risk for drug addiction. However, the mechanisms of such trans-generational effects of drugs are not so clear. Here we have evaluated the effects of parental morphine consumption on anxiety, morphine preference, and mRNA expression of dopamine receptors in F1 and F2 male offspring. Morphine was chronically administered to adult male and female Wistar rats followed by 14-day abstinence before mating. Morphine preference and anxiety-like behavior in the offspring were measured by two-bottle-choice paradigm and elevated-plus maze, respectively. Real-time PCR was used to measure the mRNA expression level of dopamine receptors in the striatum, nucleus accumbens, prefrontal cortex, and hippocampus of F1 animals. The results indicated that F1 but not the F2 male progeny of morphine-exposed parents had a greater preference for morphine, and more anxiety-like behavior compared to the offspring of saline-treated parents. In F1 male progeny of morphine-treated parents, D1 and D5 dopamine receptors were significantly increased in the prefrontal cortex and nucleus accumbens. D5 and D2 receptors were decreased in the hippocampus. D4 dopamine receptor was augmented in striatum and hippocampus and decreased in the prefrontal cortex. Adulthood exposure to chronic morphine in male and female rats before conception leads to higher morphine preference and increased anxiety in F1 but not F2 male progeny. Alterations of dopamine receptor expression in the reward system may be one mechanism responsible for observed changes in F1 offspring.
机译:对药物的成瘾,包括阿片类药是环境和遗传因素之间相互作用的结果。已经表明,瘾君子的后代是吸毒成瘾的风险较高。然而,这种药物的这种跨代性效应的机制并不明确。在这里,我们评估了F1和F2男性后代多巴胺受体对焦虑,吗啡偏好和mRNA表达的焦虑,吗啡偏好和mRNA表达的影响。慢性施用于成年雄性和女性Wistar大鼠的吗啡,然后在交配前进行14天的禁欲。后代的吗啡偏好和焦虑的行为分别通过两瓶选择范式和升高的迷宫测量。实时PCR用于测量纹状体,核心腺,前额外皮层和F1动物海马的多巴胺受体的mRNA表达水平。结果表明,与吗啡暴露的父母的F2雄性后代对吗啡的偏好,与盐水处理的父母的后代相比,对吗啡的偏好和更焦虑的行为。在F1雄性治疗父母的男性后代,预偏移皮质和核心腺中的D1和D5多巴胺受体显着增加。在海马中降低D5和D2受体。 D4多巴胺受体在纹状体和海马中增强,并在前额叶皮质中减少。在孕概念前对雄性和雌性大鼠的慢性吗啡暴露于慢性吗啡导致对吗啡偏好和F1中的焦虑增加而不是F2雄性后代。奖励系统中多巴胺受体表达的改变可以是负责观察到F1后代变化的一种机制。

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