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社交挫败导致厌食行为和下丘脑丙二酰辅酶 A 水平升高的大鼠模型。

Anorexic behavior and elevation of hypothalamic malonyl-CoA in socially defeated rats.

机构信息

College of Agriculture, Ibaraki University, Ami, Ibaraki 300-0393, Japan.

出版信息

Biochem Biophys Res Commun. 2012 May 4;421(2):301-4. doi: 10.1016/j.bbrc.2012.04.004. Epub 2012 Apr 7.

Abstract

Suppression of body weight and eating disorders, such as anorexia, are one of the major symptoms of psychiatric disorders such as depression. However, the mechanisms of weight loss and reduced appetite in depressive patients and in animal models of depression are largely unknown. In this study, we characterized the mechanism of anorexia resulting from depression using socially defeated rats as an animal model of depression. Socially defeated rats showed suppressed body weight gain, enlarged adrenal glands, decreased home cage activity, decreased food intake, and increased immobility in the forced swim test. These results are representative of some of the core symptoms of depression. Simultaneously, we observed decreased levels of phosphorylated AMP-activated protein kinase (AMPK) and acetyl-coenzyme A (CoA) carboxylase (ACC) and increased levels of malonyl-CoA in the hypothalamus of socially defeated rats. Hypothalamic malonyl-CoA controlled feeding behavior and elevation of malonyl-CoA in the hypothalamus induced inhibition of food intake. Our findings suggest that the suppression of body weight gain caused by social defeat stress is caused by anorexic feeding behavior via an increased concentration of malonyl-CoA in the hypothalamus.

摘要

体重减轻和饮食失调,如厌食症,是抑郁症等精神疾病的主要症状之一。然而,抑郁患者和抑郁动物模型中体重减轻和食欲下降的机制在很大程度上尚不清楚。在这项研究中,我们使用社交挫败大鼠作为抑郁的动物模型,研究了抑郁引起的厌食症的机制。社交挫败大鼠表现出体重增加减少、肾上腺增大、笼内活动减少、食物摄入量减少以及在强迫游泳试验中不动性增加。这些结果代表了一些抑郁症的核心症状。同时,我们观察到社交挫败大鼠下丘脑中磷酸化 AMP 激活的蛋白激酶(AMPK)和乙酰辅酶 A(CoA)羧化酶(ACC)的水平降低,丙二酰 CoA 的水平升高。下丘脑中的丙二酰 CoA 控制摄食行为,而丙二酰 CoA 在下丘脑中的升高会抑制食物摄入。我们的研究结果表明,社交挫败应激引起的体重减轻是由于下丘脑丙二酰 CoA 浓度升高引起的厌食性摄食行为所致。

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