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C57BL/6小鼠体内的神经肽Y消融会导致轻度肥胖,并使禁食后的再喂养反应受损。

NPY ablation in C57BL/6 mice leads to mild obesity and to an impaired refeeding response to fasting.

作者信息

Segal-Lieberman Gabriella, Trombly Daniel J, Juthani Viral, Wang Xiaomei, Maratos-Flier Eleftheria

机构信息

Department of Medicine, Harvard Medical School, Boston, Massachusetts 02215, USA.

出版信息

Am J Physiol Endocrinol Metab. 2003 Jun;284(6):E1131-9. doi: 10.1152/ajpendo.00491.2002. Epub 2003 Feb 11.

Abstract

Neuropeptide Y (NPY) is an orexigenic (appetite-stimulating) peptide that plays an important role in regulating energy balance. When administered directly into the central nervous system, animals exhibit an immediate increase in feeding behavior, and repetitive injections or chronic infusions lead to obesity. Surprisingly, initial studies of Npy(-/-) mice on a mixed genetic background did not reveal deficits in energy balance, with the exception of an attenuation in obesity seen in ob/ob mice in which the NPY gene was also deleted. Here, we show that, on a C57BL/6 background, NPY ablation is associated with an increase in body weight and adiposity and a significant defect in refeeding after a fast. This impaired refeeding response in Npy(-/-) mice resulted in a deficit in weight gain in these animals after 24 h of refeeding. These data indicate that genetic background must be taken into account when the biological role of NPY is evaluated. When examined on a C57BL/6 background, NPY is important for the normal refeeding response after starvation, and its absence promotes mild obesity.

摘要

神经肽Y(NPY)是一种促食欲(刺激食欲)的肽,在调节能量平衡中起重要作用。当直接注入中枢神经系统时,动物的进食行为会立即增加,重复注射或长期输注会导致肥胖。令人惊讶的是,对具有混合遗传背景的Npy(-/-)小鼠的初步研究并未发现能量平衡存在缺陷,但NPY基因也被敲除的ob/ob小鼠的肥胖程度有所减轻。在这里,我们表明,在C57BL/6背景下,NPY缺失与体重增加和肥胖相关,并且在禁食后的再喂养中存在明显缺陷。Npy(-/-)小鼠这种受损的再喂养反应导致这些动物在再喂养24小时后体重增加不足。这些数据表明,在评估NPY的生物学作用时必须考虑遗传背景。在C57BL/6背景下进行检查时,NPY对饥饿后的正常再喂养反应很重要,其缺失会导致轻度肥胖。

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