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膳食脂肪类型对体脂、瘦素以及弓状核瘦素受体、神经肽Y和刺鼠相关蛋白mRNA表达的影响。

Effects of dietary fat types on body fatness, leptin, and ARC leptin receptor, NPY, and AgRP mRNA expression.

作者信息

Wang Hongqin, Storlien Len H, Huang Xu-Feng

机构信息

Metabolic Research Center, Department of Biomedical Science, University of Wollongong, Wollongong, New South Wales 2522, Australia.

出版信息

Am J Physiol Endocrinol Metab. 2002 Jun;282(6):E1352-9. doi: 10.1152/ajpendo.00230.2001.

Abstract

Some, but not all, fats are obesogenic. The aim of the present studies was to investigate the effects of changing type and amount of dietary fats on energy balance, fat deposition, leptin, and leptin-related neural peptides: leptin receptor, neuropeptide Y (NPY), agouti-related peptide (AgRP), and proopiomelanocortin (POMC), in C57Bl/6J mice. One week of feeding with a highly saturated fat diet resulted in ~50 and 20% reduction in hypothalamic arcuate NPY and AgRP mRNA levels, respectively, compared with a low-fat or an n-3 or n-6 polyunsaturated high-fat (PUFA) diet without change in energy intake, fat mass, plasma leptin levels, and leptin receptor or POMC mRNA. Similar neuropeptide results were seen at 7 wk, but by then epididymal fat mass and plasma leptin levels were significantly elevated in the saturated fat group compared with low-fat controls. In contrast, fat and leptin levels were reduced in the n-3 PUFA group compared with all other groups. At 7 wk, changing the saturated fat group to n-3 PUFA for 4 wk completely reversed the hyperleptinemia and increased adiposity and neuropeptide changes induced by saturated fat. Changing to a low-fat diet was much less effective. In summary, a highly saturated fat diet induces obesity without hyperphagia. A regulatory reduction in NPY and AgRP mRNA levels is unable to effectively counteract this obesogenic drive. Equally high fat diets emphasizing PUFAs may even protect against obesity.

摘要

部分(而非全部)脂肪具有致肥胖性。本研究的目的是调查改变膳食脂肪的类型和数量对C57Bl/6J小鼠能量平衡、脂肪沉积、瘦素及瘦素相关神经肽(瘦素受体、神经肽Y (NPY)、刺鼠相关肽(AgRP)和阿黑皮素原(POMC))的影响。与低脂、n-3或n-6多不饱和高脂肪(PUFA)饮食相比,一周的高饱和脂肪饮食导致下丘脑弓状核NPY和AgRP mRNA水平分别降低约50%和20%,而能量摄入、脂肪量、血浆瘦素水平以及瘦素受体或POMC mRNA没有变化。在7周时观察到了类似的神经肽结果,但此时与低脂对照组相比,饱和脂肪组的附睾脂肪量和血浆瘦素水平显著升高。相比之下,n-3 PUFA组的脂肪和瘦素水平低于所有其他组。在7周时,将饱和脂肪组改为n-3 PUFA 4周可完全逆转饱和脂肪诱导的高瘦素血症、肥胖增加和神经肽变化。改为低脂饮食的效果则要差得多。总之,高饱和脂肪饮食可导致肥胖而无食欲亢进。NPY和AgRP mRNA水平的调节性降低无法有效对抗这种致肥胖驱动力。同样,强调PUFA的高脂肪饮食甚至可能预防肥胖。

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