Institute of Biological and Environmental Sciences (IBES), University of Aberdeen, Aberdeen AB39 2PN, Scotland, UK.
Mol Metab. 2012 Nov 2;2(2):103-8. doi: 10.1016/j.molmet.2012.10.003. eCollection 2012.
Obesity is at epidemic proportions but treatment options remain limited. Treatment of obesity by calorie restriction (CR) despite having initial success often fails due to rebound weight gain. One possibility is that this reflects an increased body weight (BW) set-point. Indeed, high fat diets (HFD) reduce adult neurogenesis altering hypothalamic neuroarchitecture. However, it is uncertain if these changes are associated with weight rebound or if long-term weight management is associated with reversing this. Here we show that obese mice have an increased BW set-point and lowering this set-point is associated with rescuing hypothalamic remodelling. Treating obesity by CR using HFD causes weight loss, but not rescued remodelling resulting in rebound weight gain. However, treating obesity by CR using non-HFD causes weight loss, rescued remodelling and attenuates rebound weight gain. We propose that these phenomena may explain why successful short-term weight loss improves obesity in some people but not in others.
肥胖是一种流行的疾病,但治疗方法仍然有限。尽管卡路里限制 (CR) 治疗肥胖症最初取得了成功,但由于体重反弹,往往会失败。一种可能性是,这反映了体重设定点的增加。事实上,高脂肪饮食 (HFD) 会减少成年神经发生,改变下丘脑神经结构。然而,目前还不确定这些变化是否与体重反弹有关,或者长期体重管理是否与逆转这种情况有关。在这里,我们表明肥胖小鼠的体重设定点增加,降低这个设定点与挽救下丘脑重塑有关。使用 HFD 的 CR 治疗肥胖症会导致体重减轻,但不会挽救重塑,从而导致体重反弹。然而,使用非 HFD 的 CR 治疗肥胖症会导致体重减轻、挽救重塑和减轻体重反弹。我们提出,这些现象可能解释了为什么短期成功减肥可以改善一些人的肥胖症,但对其他人却没有效果。