Jéquier E, Tappy L
Institute of Physiology, University of Lausanne, Lausanne, Switzerland.
Physiol Rev. 1999 Apr;79(2):451-80. doi: 10.1152/physrev.1999.79.2.451.
The mechanisms involved in body weight regulation in humans include genetic, physiological, and behavioral factors. Stability of body weight and body composition requires that energy intake matches energy expenditure and that nutrient balance is achieved. Human obesity is usually associated with high rates of energy expenditure. In adult individuals, protein and carbohydrate stores vary relatively little, whereas adipose tissue mass may change markedly. A feedback regulatory loop with three distinct steps has been recently identified in rodents: 1) a sensor that monitors the size of adipose tissue mass is represented by the amount of leptin synthesized by adipose cells (a protein encoded by the ob gene) which determines the plasma leptin levels; 2) hypothalamic centers, with specific leptin receptors, which receive and integrate the intensity of the signal; and 3) effector systems that influence the two determinants of energy balance, i.e., energy intake and energy expenditure. With the exception of a few very rare cases, the majority of obese human subjects have high plasma leptin levels that are related to the size of their adipose tissue mass. However, the expected regulatory responses (reduction in food intake and increase in energy expenditure) are not observed in obese individuals. Thus obese humans are resistant to the effect of endogenous leptin, despite unaltered hypothalamic leptin receptors. Whether defects in the leptin signaling cascade play a role in the development of human obesity is a field of great actual interest that needs further research. Present evidences suggest that genetic and environmental factors influence eating behavior of people prone to obesity and that diets that are high in fat or energy dense undermine body weight regulation by promoting an overconsumption of energy relative to need.
人类体重调节涉及的机制包括遗传、生理和行为因素。体重和身体成分的稳定要求能量摄入与能量消耗相匹配,并实现营养平衡。人类肥胖通常与高能量消耗率有关。在成年人中,蛋白质和碳水化合物储存变化相对较小,而脂肪组织量可能会有显著变化。最近在啮齿动物中发现了一个具有三个不同步骤的反馈调节回路:1)监测脂肪组织量大小的传感器由脂肪细胞合成的瘦素量(由ob基因编码的一种蛋白质)代表,它决定血浆瘦素水平;2)具有特定瘦素受体的下丘脑中心,接收并整合信号强度;3)影响能量平衡的两个决定因素,即能量摄入和能量消耗的效应系统。除了极少数非常罕见的情况外,大多数肥胖人类受试者的血浆瘦素水平较高,这与他们脂肪组织的大小有关。然而,肥胖个体并未观察到预期的调节反应(食物摄入量减少和能量消耗增加)。因此,尽管下丘脑瘦素受体未改变,但肥胖人类对内源性瘦素的作用具有抗性。瘦素信号级联缺陷是否在人类肥胖的发生中起作用是一个当前备受关注的领域,需要进一步研究。目前的证据表明,遗传和环境因素会影响易肥胖人群的饮食行为,高脂肪或高能量密度的饮食会通过促进能量摄入超过需求来破坏体重调节。