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有证据表明,有一种非瘦素系统可以防止过度喂养引起的体重增加。

Evidence for a Non-leptin System that Defends against Weight Gain in Overfeeding.

机构信息

Department of Medicine, Naomi Berrie Diabetes Center, Columbia University, 1150 St. Nicholas Avenue, New York, NY 10032, USA.

Department of Pediatrics, Naomi Berrie Diabetes Center, Columbia University, 1150 St. Nicholas Avenue, New York, NY 10032, USA.

出版信息

Cell Metab. 2018 Aug 7;28(2):289-299.e5. doi: 10.1016/j.cmet.2018.05.029. Epub 2018 Jun 21.

Abstract

Weight is defended so that increases or decreases in body mass elicit responses that favor restoration of one's previous weight. While much is known about the signals that respond to weight loss and the central role that leptin plays, the lack of experimental systems studying the overfed state has meant little is known about pathways defending against weight gain. We developed a system to study this physiology and found that overfed mice defend against increased weight gain with graded anorexia but, unlike weight loss, this response is independent of circulating leptin concentration. In overfed mice that are unresponsive to orexigenic stimuli, adipose tissue is transcriptionally and immunologically distinct from fat of ad libitum-fed obese animals. These findings provide evidence that overfeeding-induced obesity alters adipose tissue and central responses in ways that are distinct from ad libitum obesity and activates a non-leptin system to defend against weight gain.

摘要

体重是有保护机制的,因此体重增加或减少会引发有利于恢复之前体重的反应。虽然人们已经了解了响应体重减轻的信号以及瘦素在其中的核心作用,但由于缺乏研究过度进食状态的实验系统,人们对抵御体重增加的途径知之甚少。我们开发了一种研究这种生理学的系统,发现过度进食的小鼠会通过逐渐出现厌食来抵御体重增加,但与体重减轻不同,这种反应不依赖于循环瘦素浓度。在对食欲刺激无反应的过度进食小鼠中,脂肪组织在转录和免疫上与自由进食肥胖动物的脂肪不同。这些发现提供了证据,表明过度喂养引起的肥胖以不同于自由进食肥胖的方式改变脂肪组织和中枢反应,并激活非瘦素系统来抵御体重增加。

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