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本文引用的文献

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Fetal and neonatal pathways to obesity.胎儿和新生儿期肥胖的发展路径。
Front Horm Res. 2008;36:61-72. doi: 10.1159/000115337.
2
The brain, appetite, and obesity.大脑、食欲与肥胖
Annu Rev Psychol. 2008;59:55-92. doi: 10.1146/annurev.psych.59.103006.093551.
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Induction of central leptin resistance in hyperphagic pseudopregnant rats by chronic prolactin infusion.通过慢性输注催乳素来诱导食欲亢进的假孕大鼠产生中枢性瘦素抵抗。
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Hypothalamic phosphatidylinositol 3-kinase pathway of leptin signaling is impaired during the development of diet-induced obesity in FVB/N mice.在FVB/N小鼠饮食诱导肥胖的发展过程中,瘦素信号的下丘脑磷脂酰肌醇3-激酶途径受损。
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The integrative role of CNS fuel-sensing mechanisms in energy balance and glucose regulation.中枢神经系统燃料感知机制在能量平衡和葡萄糖调节中的整合作用。
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Leptin replacement alters brain response to food cues in genetically leptin-deficient adults.在基因瘦素缺乏的成年人中,补充瘦素会改变大脑对食物线索的反应。
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Mechanisms of leptin action and leptin resistance.瘦素的作用机制与瘦素抵抗
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Leptin regulates striatal regions and human eating behavior.瘦素调节纹状体区域和人类的饮食行为。
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A nonadaptive scenario explaining the genetic predisposition to obesity: the "predation release" hypothesis.一种解释肥胖遗传易感性的非适应性情形:“捕食释放”假说。
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Why some of us get fat and what we can do about it.为什么我们中的一些人会发胖以及我们对此能做些什么。
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瘦素抵抗与对正能量平衡的反应。

Leptin resistance and the response to positive energy balance.

作者信息

Morrison Christopher D

机构信息

Pennington Biomedical Research Center, Baton Rouge, LA 70808, USA.

出版信息

Physiol Behav. 2008 Aug 6;94(5):660-3. doi: 10.1016/j.physbeh.2008.04.009. Epub 2008 Apr 12.

DOI:10.1016/j.physbeh.2008.04.009
PMID:18508097
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2517010/
Abstract

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.

摘要

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。