Department of Neurobiology, Weizmann Institute of Science, Rehovot, 76100, Israel; Department of Stress Neurobiology and Neurogenetics, Max Planck Institute of Psychiatry, Munich, 80804, Germany.
Department of Stress Neurobiology and Neurogenetics, Max Planck Institute of Psychiatry, Munich, 80804, Germany.
Mol Metab. 2018 Nov;17:1-16. doi: 10.1016/j.molmet.2018.08.005. Epub 2018 Aug 20.
Vulnerability to eating disorders (EDs) is broadly assumed to be associated with early life stress. However, a careful examination of the literature shows that susceptibility to EDs may depend on the type, severity and timing of the stressor and the sex of the individual. We aimed at exploring the link between chronic prenatal stress and predisposition to EDs and metabolic disease.
We used a chronic variable stress protocol during gestation to explore the metabolic response of male and female offspring to food restriction (FR), activity-based anorexia (ABA), binge eating (BE) and exposure to high fat (HF) diet.
Contrary to controls, prenatally stressed (PNS) female offspring showed resistance to ABA and BE and displayed a lower metabolic rate leading to hyperadiposity and obesity on HF diet. Male PNS offspring showed healthy responses to FR and ABA, increased propensity to binge and improved coping with HF compared to controls. We found that long-lasting abnormal responses to metabolic challenge are linked to fetal programming and adult hypothalamic dysregulation in PNS females, resulting from sexually dimorphic adaptations in placental methylation and gene expression.
Our results show that maternal stress may have variable and even opposing effects on ED risk, depending on the ED and the sex of the offspring.
人们普遍认为,易患饮食失调症(EDs)与早期生活压力有关。然而,仔细研究文献表明,易患 EDs 的可能性可能取决于压力源的类型、严重程度和时间以及个体的性别。我们旨在探索慢性产前应激与 EDs 和代谢性疾病易感性之间的联系。
我们在妊娠期使用慢性可变应激方案,探索雄性和雌性后代对食物限制(FR)、基于活动的厌食症(ABA)、暴食(BE)和暴露于高脂肪(HF)饮食的代谢反应。
与对照组相比,产前应激(PNS)的雌性后代对 ABA 和 BE 表现出抵抗力,并且代谢率较低,导致在 HF 饮食下出现肥胖和肥胖。与对照组相比,雄性 PNS 后代对 FR 和 ABA 表现出健康的反应,暴食倾向增加,并且对 HF 饮食的适应能力提高。我们发现,对代谢挑战的持久异常反应与胎儿编程和 PNS 雌性成年下丘脑失调有关,这是由于胎盘甲基化和基因表达的性别二态性适应所致。
我们的研究结果表明,母体应激可能对 ED 风险产生可变的甚至相反的影响,具体取决于 ED 和后代的性别。