每日 GDF15 处理对小鼠体重和食物摄入量的影响具有性别特异性,并且不会增强小鼠自愿体力活动的效果。

IF 4.7 2区 医学 Q1 NEUROSCIENCES
Stewart Jeromson, Michael Akcan, Bradley Baranowski, Meagan Arbeau, Annalaura Bellucci, David C. Wright
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引用次数: 0

摘要

生长分化因子 15(GDF15)是一种由压力诱导的细胞因子,可抑制食物摄入量并减轻体重。GDF15 还会减少自愿体力活动,因此,目前还不清楚将 GDF15 与运动相结合是否有益,也不清楚食物摄入量的减少是否会被体力活动的减少所抵消。我们研究了 GDF15 治疗与自愿轮跑(VWR)相结合会如何影响小鼠的体重增加、食物摄入量、脂肪含量和代谢健康指数。高脂喂养的雄性和雌性小鼠每天都要接受 GDF15 治疗,并在 11 天内可以接触或不接触自主跑步轮。在雌雄小鼠中,VWR都能防止体重增加。在雄性小鼠中,GDF15可减少食物摄入量,减轻体重增加和脂肪组织堆积,而VWR则没有额外的效果。对于雌性小鼠,GDF15 不会影响体重增加或身体组成。GDF15 会急性减少雌性小鼠的食物摄入量,但随后会出现一段时间的反弹性多食,因此 GDF15 不会减少雌性小鼠的总食物摄入量。GDF15处理会减少雌雄小鼠的轮跑距离。VWR对改善雌性小鼠的葡萄糖耐量有主要作用,但对雄性小鼠没有作用。这些研究结果表明,GDF15对食物摄入量有性别特异性影响,因此也会影响体重增加和肥胖。将GDF15和自愿体育锻炼结合在一起对减肥没有额外的益处。GDF15诱导的急性热量限制的适应性反应可能会限制其作为雌性减肥工具的有效性。要点:GDF15 是一种应激诱导信号因子,可减少食物摄入量和自主体育锻炼。目前尚不清楚将 GDF15 治疗与自愿轮跑相结合是否会在减轻体重增加和脂肪组织堆积方面产生有益的综合效应。在本研究中,我们证明了 GDF15 能减少雄性小鼠的食物摄入量并防止体重增加,但不能防止雌性小鼠摄入高脂肪饮食。在雌性小鼠中,GDF15会急性降低食物摄入量,但随后会出现一段时间的反弹性多食,导致总食物摄入量没有差异。在雌雄小鼠中,VWR 在防止体重增加方面的作用与 GDF15 相当,甚至优于 GDF15。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Daily GDF15 treatment has sex-specific effects on body weight and food intake and does not enhance the effects of voluntary physical activity in mice

Daily GDF15 treatment has sex-specific effects on body weight and food intake and does not enhance the effects of voluntary physical activity in mice
Growth differentiation factor 15 (GDF15) is a stress-induced cytokine that suppresses food intake and causes weight loss. GDF15 also reduces voluntary physical activity and, thus, it is not clear whether combining GDF15 with exercise will be beneficial or if reductions in food intake would be offset by decreases in physical activity. We investigated how GDF15 treatment combined with voluntary wheel running (VWR) would impact weight gain, food intake, adiposity and indices of metabolic health in mice. High-fat fed male and female mice underwent daily GDF15 treatments and were given access to voluntary running wheels, or not, for 11 days. In both sexes, VWR prevented weight gain. In males, GDF15 reduced food intake, as well as attenuated weight gain and the accumulation of adipose tissue, with no additional effect of VWR. In female mice, GDF15 did not impact body weight gain or body composition. GDF15 acutely reduced food intake in female mice but this was followed by a period of rebound hyperphagia and consequently GDF15 did not reduce total food intake in female mice. GDF15 treatment reduced wheel running distance in both sexes. There were main effects of VWR to improve glucose tolerance in female but not male mice. These findings show that GDF15 has sex-specific effects on food intake and consequently weight gain and adiposity. There is no added benefit of combining GDF15 and voluntary physical activity for weight loss. Adaptive responses to acute caloric restriction induced by GDF15 might limit its effectiveness as a weight loss tool in females.

Key points

  • GDF15 is a stress-induced signalling factor that reduces food intake and voluntary physical activity.
  • It is not known whether combining GDF15 treatment with voluntary wheel running would impart beneficial combined effects in attenuating weight gain and the accumulation of adipose tissue.
  • In the present study, we demonstrate that GDF15 reduces food intake and prevents weight gain in male but not female mice consuming a high-fat diet and also that combining GDF15 with voluntary wheel running (VWR) does not lead to a greater dampening of weight gain.
  • In female mice, GDF15 acutely reduced food intake, but this was followed by a period of rebound hyperphagia resulting in no differences in total food intake.
  • In both sexes, VWR was equivalent, or superior to GDF15 in preventing weight gain.
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来源期刊
Journal of Physiology-London
Journal of Physiology-London 医学-神经科学
CiteScore
9.70
自引率
7.30%
发文量
817
审稿时长
2 months
期刊介绍: The Journal of Physiology publishes full-length original Research Papers and Techniques for Physiology, which are short papers aimed at disseminating new techniques for physiological research. Articles solicited by the Editorial Board include Perspectives, Symposium Reports and Topical Reviews, which highlight areas of special physiological interest. CrossTalk articles are short editorial-style invited articles framing a debate between experts in the field on controversial topics. Letters to the Editor and Journal Club articles are also published. All categories of papers are subjected to peer reivew. The Journal of Physiology welcomes submitted research papers in all areas of physiology. Authors should present original work that illustrates new physiological principles or mechanisms. Papers on work at the molecular level, at the level of the cell membrane, single cells, tissues or organs and on systems physiology are all acceptable. Theoretical papers and papers that use computational models to further our understanding of physiological processes will be considered if based on experimentally derived data and if the hypothesis advanced is directly amenable to experimental testing. While emphasis is on human and mammalian physiology, work on lower vertebrate or invertebrate preparations may be suitable if it furthers the understanding of the functioning of other organisms including mammals.
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