Romaní-Pérez M, Lépinay A L, Alonso L, Rincel M, Xia L, Fanet H, Caillé S, Cador M, Layé S, Vancassel S, Darnaudéry M
INRA, Nutrition et Neurobiologie Intégrée, UMR1286, Bordeaux, France.
Université de Bordeaux, Nutrition et Neurobiologie Intégrée, UMR1286, Bordeaux, France.
Int J Obes (Lond). 2017 Apr;41(4):502-509. doi: 10.1038/ijo.2016.236. Epub 2016 Dec 27.
BACKGROUND/OBJECTIVES: Energy-dense food exposure and stress during development have been suggested to contribute to obesity and metabolic disorders later in life. Although these factors are frequently associated, the effects of their combination have not yet been investigated. In this study, using an animal model, we examined the long-term impact of maternal high-fat diet (HFD) and early-life stress (ELS) on energy homoeostasis control and food motivation.
Body weight growth under HFD, adipose tissue, body weight control in response to fasting and refeeding, food-motivated behaviour and mesolimbic dopamine function were examined in adult male offspring exposed to maternal HFD (during gestation and lactation) and/or ELS (maternal separation 3 h per day from postnatal day 2 to 14).
Maternal HFD or ELS alone had no significant effect on offspring body weight; however, the combination of these factors exacerbated body weight gain when animals were exposed to HFD after weaning. There are no other significant combinatory effects of these perinatal events. In contrast, independently of the maternal diet, ELS disrupted body weight control during a fasting-refeeding procedure, increased adipose tissue mass and altered lipid metabolism. Finally, maternal HFD and ELS both resulted in exacerbated food-motivated behaviour and blunted dopamine release in the nucleus accumbens during palatable food consumption.
We report a synergistic effect of perinatal HFD exposure and stress on the susceptibility to gain weight under HFD. However, ELS has a stronger impact than maternal HFD exposure on energy homoeostasis and food motivation in adult offspring. Altogether, our results suggest a programming effect of stress and nutrition supporting the hypothesis of the developmental origin of health and disease.
背景/目的:有研究表明,发育期间接触高能量密度食物以及压力会导致日后肥胖和代谢紊乱。尽管这些因素常常同时出现,但它们共同作用的影响尚未得到研究。在本研究中,我们使用动物模型,研究了母体高脂饮食(HFD)和生命早期应激(ELS)对能量稳态控制和食物动机的长期影响。
对在孕期和哺乳期接触母体HFD和/或ELS(从出生后第2天到第14天,每天母体分离3小时)的成年雄性后代,检测其在HFD下的体重增长、脂肪组织、禁食和再喂食后的体重控制、食物动机行为以及中脑边缘多巴胺功能。
单独的母体HFD或ELS对后代体重没有显著影响;然而,当动物在断奶后接触HFD时,这些因素共同作用会加剧体重增加。这些围产期事件没有其他显著的联合作用。相比之下,不考虑母体饮食,ELS会在禁食-再喂食过程中破坏体重控制,增加脂肪组织量并改变脂质代谢。最后,母体HFD和ELS都会导致食物动机行为加剧,并且在食用美味食物期间伏隔核中的多巴胺释放减弱。
我们报告了围产期HFD暴露和应激对HFD下体重增加易感性的协同作用。然而,在成年后代中,ELS对能量稳态和食物动机的影响比母体HFD暴露更强。总之,我们的结果表明应激和营养具有编程效应,支持健康与疾病发育起源的假说。