Gac L, Kanaly V, Ramirez V, Teske J A, Pinto M P, Perez-Leighton C E
Center for Integrative Medicine and Innovative Science, Facultad de Medicina, Universidad Andres Bello, Santiago, Region Metropolitana 8370071, Chile.
Department of Nutritional Sciences, University of Arizona, Tucson, AZ USA; Minneapolis VA Health Care System, Minneapolis, MN 55417, USA; Minnesota Obesity Center, University of Minnesota, Saint Paul, MN 55108, USA.
Physiol Behav. 2015 Dec 1;152(Pt A):315-22. doi: 10.1016/j.physbeh.2015.10.001. Epub 2015 Oct 9.
Despite the increase in obesity prevalence over the last decades, humans show large inter-individual variability for susceptibility to diet-induced obesity. Understanding the biological basis of this susceptibility could identify new therapeutic alternatives against obesity. We characterized behavioral changes associated with propensity to obesity induced by cafeteria (CAF) diet consumption in mice. We show that Balb/c mice fed a CAF diet display a large inter-individual variability in susceptibility to diet-induced obesity, such that based on changes in adiposity we can classify mice as obesity prone (OP) or obesity resistant (OR). Both OP and OR were hyperphagic relative to control-fed mice but caloric intake was similar between OP and OR mice. In contrast, OR had a larger increase in locomotor activity following CAF diet compared to OP mice. Obesity resistant and prone mice showed similar intake of sweet snacks, but OR ate more savory snacks than OP mice. Two bottle sucrose preference tests showed that OP decreased their sucrose preference compared to OR mice after CAF diet feeding. Finally, to test the robustness of the OR phenotype in response to further increases in caloric intake, we fed OR mice with a personalized CAF (CAF-P) diet based on individual snack preferences. When fed a CAF-P diet, OR increased their calorie intake compared to OP mice fed the standard CAF diet, but did not reach adiposity levels observed in OP mice. Together, our data show the contribution of hedonic intake, individual snack preference and physical activity to individual susceptibility to obesity in Balb/c mice fed a standard and personalized cafeteria-style diet.
尽管在过去几十年里肥胖患病率有所上升,但人类在饮食诱导性肥胖易感性方面存在很大的个体差异。了解这种易感性的生物学基础可以确定对抗肥胖的新治疗方法。我们对小鼠食用自助餐厅(CAF)饮食诱导肥胖倾向相关的行为变化进行了表征。我们发现,喂食CAF饮食的Balb/c小鼠在饮食诱导性肥胖易感性方面表现出很大的个体差异,因此根据肥胖程度的变化,我们可以将小鼠分为肥胖倾向(OP)或肥胖抵抗(OR)。相对于对照喂养的小鼠,OP和OR均出现食欲亢进,但OP和OR小鼠的热量摄入相似。相比之下,与OP小鼠相比,CAF饮食后OR的运动活动增加幅度更大。肥胖抵抗和肥胖倾向小鼠对甜味零食的摄入量相似,但OR比OP小鼠吃更多的咸味零食。两项双瓶蔗糖偏好试验表明,CAF饮食喂养后,与OR小鼠相比,OP降低了它们对蔗糖的偏好。最后,为了测试OR表型对热量摄入进一步增加的反应的稳健性,我们根据个体零食偏好为OR小鼠喂食个性化的CAF(CAF-P)饮食。当喂食CAF-P饮食时,与喂食标准CAF饮食的OP小鼠相比,OR增加了它们的热量摄入,但未达到OP小鼠中观察到的肥胖水平。总之,我们的数据显示了享乐性摄入、个体零食偏好和身体活动对喂食标准和个性化自助餐厅式饮食的Balb/c小鼠个体肥胖易感性的影响。