Archer Zoë A, Mercer Julian G
Division of Obesity and Metabolic Health, Rowett Research Institute, Aberdeen AB21 9SB, UK.
Proc Nutr Soc. 2007 Feb;66(1):124-30. doi: 10.1017/S0029665107005356.
Rodent models of diet-induced obesity (DIO) mimic common human obesity more accurately than obese single-gene mutation lines, such as the ob/ob mouse. Sprague-Dawley rats sourced in the UK develop obesity when fed a high-energy diet, but susceptibility to DIO is normally distributed, as might be anticipated for a polygenic trait in an outbred population, in contrast to reports in the literature using ostensibly the same strain of rats sourced in the USA. Nevertheless, the responses of these rats to solid and liquid obesogenic diets are very similar to those reported elsewhere, and this model of DIO has much to commend it as a vehicle for the mechanistic study of susceptibility to DIO, development and reversal of obesity on solid and liquid diets and the response of peripheral and central energy balance systems to the development of obesity and to the obesogenic diets themselves. In general, hypothalamic energy-balance-related systems respond to obesogenic diets and developing obesity with activity changes that appear designed to counter the further development of the obese state. However, these hypothalamic changes are apparently unable to maintain body weight and composition within normal limits, suggesting that attributes of the obesogenic diets either evade the normal regulatory systems and/or engage with reward pathways that override the homeostatic systems. Since diets are a risk factor in the development of obesity, it will be important to establish how obesogenic diets interact with energy-balance pathways and whether there is potential for diets to be manipulated with therapeutic benefit.
与肥胖单基因突变品系(如ob/ob小鼠)相比,饮食诱导肥胖(DIO)的啮齿动物模型能更准确地模拟常见的人类肥胖。从英国采购的斯普拉格-道利大鼠在喂食高能量饮食时会发胖,但对DIO的易感性呈正态分布,这正如预期的那样是一个远交群体中多基因性状的情况,这与文献中使用表面上相同品系但从美国采购的大鼠的报道形成对比。尽管如此,这些大鼠对固体和液体致肥胖饮食的反应与其他地方报道的非常相似,并且这种DIO模型作为研究DIO易感性、固体和液体饮食中肥胖的发生与逆转以及外周和中枢能量平衡系统对肥胖发展和致肥胖饮食本身的反应的机制研究工具,有很多值得称赞之处。一般来说,下丘脑能量平衡相关系统对致肥胖饮食和肥胖发展的反应是活动变化,这些变化似乎旨在对抗肥胖状态的进一步发展。然而,这些下丘脑变化显然无法将体重和身体组成维持在正常范围内,这表明致肥胖饮食的特性要么避开了正常调节系统,要么与凌驾于稳态系统之上的奖赏途径相互作用。由于饮食是肥胖发展的一个风险因素,确定致肥胖饮食如何与能量平衡途径相互作用以及饮食是否有被操控以获得治疗益处的潜力将很重要。