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首页> 外文期刊>The international journal of neuropsychopharmacology >Adolescent Intermittent Ethanol Exposure Is Associated with Increased Risky Choice and Decreased Dopaminergic and Cholinergic Neuron Markers in Adult Rats
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Adolescent Intermittent Ethanol Exposure Is Associated with Increased Risky Choice and Decreased Dopaminergic and Cholinergic Neuron Markers in Adult Rats

机译:青少年间歇性乙醇暴露与成年大鼠的风险选择增加和多巴胺能和胆碱能神经元标志物减少有关。

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Background: Binge drinking is prevalent during adolescence and may have effects on the adult brain and behavior. The present study investigated whether adolescent intermittent ethanol exposure alters adult risky choice and prefrontal dopaminergic and forebrain cholinergic neuronal marker levels in male Wistar rats. Methods: Adolescent (postnatal day 28–53) rats were administered 5g/kg of 25% (vol/vol) ethanol 3 times/d in a 2-days–on/2-days–off exposure pattern. In adulthood, risky choice was assessed in the probability discounting task with descending and ascending series of large reward probabilities and after acute ethanol challenge. Immunohistochemical analyses assessed tyrosine hydroxylase, a marker of dopamine and norepinephrine in the prelimbic and infralimbic cortices, and choline acetyltransferase, a marker of cholinergic neurons, in the basal forebrain. Results: All of the rats preferred the large reward when it was delivered with high probability. When the large reward became unlikely, control rats preferred the smaller, safe reward, whereas adolescent intermittent ethanol-exposed rats continued to prefer the risky alternative. Acute ethanol had no effect on risky choice in either group of rats. Tyrosine hydroxylase (prelimbic cortex only) and choline acetyltransferase immunoreactivity levels were decreased in adolescent intermittent ethanol-exposed rats compared with controls. Risky choice was negatively correlated with choline acetyltransferase, implicating decreased forebrain cholinergic activity in risky choice. Conclusions: The decreases in tyrosine hydroxylase and choline acetyltransferase immunoreactivity suggest that adolescent intermittent ethanol exposure has enduring neural effects that may lead to altered adult behaviors, such as increased risky decision making. In humans, increased risky decision making could lead to maladaptive, potentially harmful consequences.
机译:背景:暴饮暴食在青春期很普遍,可能对成年大脑和行为产生影响。本研究调查了青春期间歇性乙醇暴露是否会改变雄性Wistar大鼠的成年危险选择以及前额叶多巴胺能和前脑胆碱能神经元标志物水平。方法:青春期(出生后第28-53天)大鼠以2天– 2天–非接触方式每天3次/ d服用5g / kg的25%(体积/体积)乙醇。在成年期,在概率折现任务中对风险选择进行了评估,其中大的奖赏概率由大到小依次下降和上升以及在急性乙醇攻击后。免疫组织化学分析评估了前脑和下肢皮质中多巴胺和去甲肾上腺素的标志物酪氨酸羟化酶,以及基底前脑中胆碱能神经元的标志物胆碱乙酰基转移酶。结果:所有大鼠均以较高的概率获得较大奖励。当获得大笔奖励变得不太可能时,对照组的老鼠会选择较小的安全奖励,而青春期间歇性暴露于乙醇的老鼠继续偏向有风险的选择。急性乙醇对两组大鼠的风险选择均无影响。与对照组相比,青春期间歇性乙醇暴露大鼠的酪氨酸羟化酶(仅前肢皮质)和胆碱乙酰转移酶免疫反应性水平降低。危险选择与胆碱乙酰基转移酶呈负相关,暗示在危险选择中前脑胆碱能活性降低。结论:酪氨酸羟化酶和胆碱乙酰基转移酶免疫反应性的降低表明,青少年间歇性乙醇暴露具有持久的神经作用,可能导致成人行为改变,例如增加危险的决策。在人类中,风险决策的增加可能导致适应不良,潜在有害的后果。

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