Nutrition Obesity Research Center, Department of Medicine, St. Luke's-Roosevelt Hospital, and Columbia University Institute of Human Nutrition, New York, NY, USA.
Adv Nutr. 2013 Mar 1;4(2):164-75. doi: 10.3945/an.112.003152.
Classically, leptin resistance has been associated with increased body fat and circulating leptin levels, and the condition is believed to contribute to the onset and/or maintenance of obesity. Although a great deal is known about the central nervous system mechanisms mediating leptin resistance, considerably less is known about the role of diet in establishing and maintaining this altered hormonal state. An exciting new finding has recently been published demonstrating the existence of leptin resistance in normal-weight rats with lean leptin levels by feeding them a high-concentration-fructose diet. This finding has opened the possibility that specific macronutrients may be capable of inducing leptin resistance, independently of the amount of body fat or circulating leptin present in the treated animals. This review describes several lines of research that have recently emerged indicating that specific types of dietary sugars and fats are capable of inducing leptin resistance in experimental rodent models. The results further show that diet-induced leptin resistance is capable of increasing energy intake and elevating body weight gain under appropriate dietary challenges. It appears that biological mechanisms on multiple levels may underlie the dietary induction of leptin resistance, including alterations in the leptin blood-to-brain transport system, in peripheral glucose metabolism, and in central leptin receptor signaling pathways. What is clear from the findings reviewed here is that diet-induced leptin resistance can occur in the absence of elevated circulating leptin levels and body weight, rendering it a potential cause and/or predisposing factor to excess body weight gain and obesity.
经典理论认为,瘦素抵抗与体脂增加和循环瘦素水平升高有关,而且该病症被认为是导致肥胖发生和/或维持的原因之一。虽然人们对介导瘦素抵抗的中枢神经系统机制有了很多了解,但对于饮食在建立和维持这种改变的激素状态中的作用却知之甚少。最近发表的一项令人兴奋的新发现表明,通过给正常体重、瘦素水平正常的大鼠喂食高浓度果糖饮食,这些大鼠会出现瘦素抵抗。这一发现使人们有可能认为,某些特定的宏量营养素可能能够独立于处理动物体内的体脂或循环瘦素含量而引起瘦素抵抗。这篇综述描述了最近出现的几项研究,这些研究表明,某些类型的膳食糖和脂肪能够在实验性啮齿动物模型中引起瘦素抵抗。研究结果进一步表明,饮食诱导的瘦素抵抗能够在适当的饮食挑战下增加能量摄入和升高体重增加。似乎在多个层面上的生物学机制可能是饮食诱导瘦素抵抗的基础,包括改变瘦素从血液到大脑的转运系统、外周葡萄糖代谢以及中枢瘦素受体信号通路。从这里回顾的研究结果中可以清楚地看出,饮食诱导的瘦素抵抗可以在不升高循环瘦素水平和体重的情况下发生,这使其成为导致体重过度增加和肥胖的一个潜在原因和/或促成因素。