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中脑边缘奖励神经回路在预防和挽救大鼠活动限制型厌食症(ABA)表型中的作用。

The Role of Mesolimbic Reward Neurocircuitry in Prevention and Rescue of the Activity-Based Anorexia (ABA) Phenotype in Rats.

机构信息

Department of Physiology, Monash University, Clayton, VIC, Australia.

出版信息

Neuropsychopharmacology. 2017 Nov;42(12):2292-2300. doi: 10.1038/npp.2017.63. Epub 2017 Mar 21.

Abstract

Patients suffering from anorexia nervosa (AN) become anhedonic; unable or unwilling to derive normal pleasures and avoid rewarding outcomes, most profoundly in food intake. The activity-based anorexia (ABA) model recapitulates many of the characteristics of the human condition, including anhedonia, and allows investigation of the underlying neurobiology of AN. The potential for increased neuronal activity in reward/hedonic circuits to prevent and rescue weight loss is investigated in this model. The mesolimbic pathway extending from the ventral tegmental area (VTA) to the nucleus accumbens (NAc) was activated using a dual viral strategy, involving retrograde transport of Cre (CAV-2-Cre) to the VTA and coincident injection of DREADD receptors (AAV-hSyn-DIO-hM3D(Gq)-mCherry). Systemic clozapine-n-oxide (CNO; 0.3 mg/kg) successfully recruited a large proportion of the VTA-NAc dopaminergic projections, with activity evidenced by colocalization with elevated levels of Fos protein. The effects of reward circuit activation on energy balance and predicted survival was investigated in female Sprague-Dawley rats, where free access to running wheels was paired with time-limited (90 min) access to food, a paradigm (ABA) which will cause anorexia and death if unchecked. Excitation of the reward pathway substantially increased food intake and food anticipatory activity (FAA) to prevent ABA-associated weight loss, while overall locomotor activity was unchanged. Similar activation of reward circuitry, delayed until establishment of the ABA phenotype, rescued rats from their precipitous weight loss. Although these data are consistent with shifts primarily in food intake, the contribution of mechanisms including energy expenditure to survival remains to be determined. These results will inform the neurobiological underpinnings of AN, and provide insight into the mechanisms of reward circuitry relevant to feeding and weight loss.

摘要

患有神经性厌食症(AN)的患者会变得快感缺失;无法或不愿意从正常的愉悦中获得乐趣,并避免获得奖励的结果,在食物摄入方面最为明显。基于活动的厌食症(ABA)模型再现了许多人类状况的特征,包括快感缺失,并允许研究 AN 的潜在神经生物学。该模型研究了增加奖励/愉悦回路中的神经元活动以预防和挽救体重减轻的潜力。使用逆行病毒(CAV-2-Cre)向 VTA 的双重病毒策略激活了从腹侧被盖区(VTA)延伸到伏隔核(NAc)的中脑边缘通路,并同时注射了 DREADD 受体(AAV-hSyn-DIO-hM3D(Gq)-mCherry)。系统给予氯氮平-N-氧化物(CNO;0.3mg/kg)可成功招募 VTA-NAc 多巴胺能投射的很大一部分,其活性通过与升高的 Fos 蛋白水平共定位来证明。在雌性 Sprague-Dawley 大鼠中研究了奖励回路激活对能量平衡和预测生存的影响,其中自由进入跑步轮与限时(90 分钟)获得食物配对,这种范式(ABA)如果不加以控制,会导致厌食和死亡。奖励途径的兴奋显著增加了食物摄入和食物预期活动(FAA),以防止与 ABA 相关的体重减轻,而整体运动活动保持不变。在建立 ABA 表型后延迟激活奖励回路,可使大鼠免于急剧的体重减轻。尽管这些数据与主要在食物摄入方面的变化一致,但能量消耗等机制对生存的贡献仍有待确定。这些结果将为 AN 的神经生物学基础提供信息,并深入了解与进食和体重减轻相关的奖励回路的机制。

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