首页> 美国卫生研究院文献>iScience >Ablation of Ventral Midbrain/Pons GABA Neurons Induces Mania-like Behaviors with Altered Sleep Homeostasis and Dopamine D2R-mediated Sleep Reduction
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Ablation of Ventral Midbrain/Pons GABA Neurons Induces Mania-like Behaviors with Altered Sleep Homeostasis and Dopamine D2R-mediated Sleep Reduction

机译:腹侧中脑/ PON GABA神经元的消融诱导睡眠稳态和多巴胺D2R介导的睡眠减少的炎躁狂的行为

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摘要

Individuals with the neuropsychiatric disorder mania exhibit hyperactivity, elevated mood, and a decreased need for sleep. The brain areas and neuronal populations involved in mania-like behaviors, however, have not been elucidated. In this study, we found that ablating the ventral medial midbrain/pons (VMP) GABAergic neurons induced mania-like behaviors in mice, including hyperactivity, anti-depressive behaviors, reduced anxiety, increased risk-taking behaviors, distractibility, and an extremely shortened sleep time. Strikingly, these mice also showed no rebound sleep after sleep deprivation, suggesting abnormal sleep homeostatic regulation. Dopamine D2 receptor deficiency largely abolished the sleep reduction induced by ablating the VMP GABAergic neurons without affecting the hyperactivity and anti-depressive behaviors. Our data demonstrate that VMP GABAergic neurons are involved in the expression of mania-like behaviors, which can be segregated to the short-sleep and other phenotypes on the basis of the dopamine D2 receptors.
机译:具有神经精神障碍的人胃癌表现出多动,心情升高,睡眠需要减少。然而,涉及躁狂症行为的大脑区域和神经元群体尚未阐明。在这项研究中,我们发现消融腹侧中脑/ PON(VMP)胃肠杆菌(VMP)诱导小鼠的躁狂症的行为,包括多动,抗抑郁行为,减少焦虑,增加风险行为,令人满意的行为,分心性和极其缩短睡觉时间。令人惊讶的是,这些小鼠在睡眠剥夺后也没有出现反弹睡眠,表明睡眠异常监管异常。多巴胺D2受体缺陷在很大程度上废除了通过烧蚀VMP胃肠杆菌的睡眠减少而不影响多动和抗抑郁行为。我们的数据表明,VMP Gabaeric神经元参与躁狂的行为的表达,其可以在多巴胺D2受体的基础上被隔离到短睡眠和其他表型。

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