Morrison Christopher D
Pennington Biomedical Research Center, Baton Rouge, LA 70808, USA.
Physiol Behav. 2008 Aug 6;94(5):660-3. doi: 10.1016/j.physbeh.2008.04.009. Epub 2008 Apr 12.
Animals readily reduce food intake and normalize body weight following a period of involuntary overfeeding, suggesting that regulatory systems are engaged to defend against excess weight gain. However, these data exist in the background of an ongoing obesity epidemic, where the ready availability of palatable, energy dense foods often leads to obesity. Currently we know very little about the mechanisms underlying the normalization of body weight following involuntary overfeeding, nor do we fully understand why select individuals successfully remain lean despite living in an obesigenic environment. Recent progress in the study of leptin signaling indicates that manipulations which enhance leptin sensitivity reduce food intake and attenuate diet-induced obesity, while reductions in leptin signaling predispose to obesity. While it remains unclear whether a failure or insufficiency in the weight regulatory system contributes to obesity, this work highlights the importance of this system for the regulation of body weight and its potential value for the treatment of obesity. Nonetheless, it is necessary to more clearly identify those mechanisms that protect lean individuals from weight gain and mediate the normalization of body weight that follows involuntary overfeeding, because it is only with this knowledge that we can clearly determine whether obesity is dependent on, or independent of, a failure in the weight regulatory system.
动物在经历一段时间的非自愿过度喂养后,会很容易减少食物摄入量并使体重恢复正常,这表明调节系统会参与其中以防止体重过度增加。然而,这些数据是在肥胖症流行的背景下出现的,在这种情况下,美味且能量密集的食物随时可得,常常会导致肥胖。目前,我们对非自愿过度喂养后体重恢复正常的潜在机制知之甚少,我们也不完全理解为什么某些个体尽管生活在致胖环境中却能成功保持消瘦。瘦素信号研究的最新进展表明,增强瘦素敏感性的操作会减少食物摄入量并减轻饮食诱导的肥胖,而瘦素信号的减少则易导致肥胖。虽然体重调节系统的功能障碍或不足是否导致肥胖仍不明确,但这项研究突出了该系统对体重调节的重要性及其在肥胖治疗中的潜在价值。尽管如此,有必要更清楚地确定那些能保护消瘦个体不增重并介导非自愿过度喂养后体重恢复正常的机制,因为只有掌握了这些知识,我们才能明确肥胖是否取决于体重调节系统的功能障碍,还是与之无关。