确认瘦素是一种新型抗肥胖脂肪因子

Jiarui Liu, Bingwei Wang, Zhijie Su, Xiaoxu Han, Miao He, Yun Zhao, Yujia Hou, Daotong Li, Weiguang Zhang, Lihua Qin, Ke Wang, Yanchun Li, Yi Yan, Siwang Yu, Xiaoshuai Huang, Tairan Yuwen, Ruimao Zheng
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引用次数: 0

摘要

脂肪因子是调节能量平衡的关键因素。我们发现了一种新型脂肪因子,并将其命名为瘦素。在人体中,白色脂肪组织中的瘦素水平与运动呈正相关,与体重指数呈负相关。瘦素水平与脂肪分解促进基因表达呈正相关。运动员血浆中的瘦素水平升高,而肥胖者血浆中的瘦素水平降低。Leptolin基因敲除小鼠的脂肪含量和体重增加,能量消耗减少。用瘦素治疗可促进脂肪动员和能量消耗,减轻体重,但不影响食物摄入和运动活动。总之,瘦素是一种新型脂肪因子,具有改善代谢状态的能力,可作为肥胖症和代谢紊乱的一种新的治疗药物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Identification of leptolin as a novel anti-obesity adipokine
Adipokines are key factors in regulating energy homeostasis. We identified a novel adipokine; we named it Leptolin. In humans, leptolin levels in white adipose tissue were positively corrected with exercise, and negatively associated with body mass index. Leptolin levels were positively correlated with lipolysis-promoting gene expression. Elevated leptolin in plasma of athletes, whereas lowered leptolin in plasma of obese individuals were observed. Leptolin gene-knockout mice exhibited increased adiposity and body weight, and decreased energy expenditure. Leptolin gene-overexpression mice showed obesity-resistant phenotypes.Treatment with leptolin promoted fat mobilization and energy expenditure, and reduced body weight, without affecting food-intake and motor activity. Together, leptolin, a novel adipokine with a capacity to improve metabolic status, may serve as a new therapeutic agent for obesity and metabolic disorders.
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