Shenzhen key laboratory for metabolic health, Center for Energy Metabolism and Reproduction, Shenzhen Institutes of Advanced Technology, Chinese Academy of Sciences, Shenzhen, 518055, P. R. China.
State Key Laboratory of Molecular Developmental Biology, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing, 100101, P. R. China.
Adv Sci (Weinh). 2023 Dec;10(35):e2305472. doi: 10.1002/advs.202305472. Epub 2023 Oct 22.
Early life nutrition can reprogram development and exert long-term consequences on body weight regulation. In mice, maternal high-fat diet (HFD) during lactation predisposed male but not female offspring to diet-induced obesity when adult. Molecular and cellular changes in the hypothalamus at important time points are examined in the early postnatal life in relation to maternal diet and demonstrated sex-differential hypothalamic reprogramming. Maternal HFD in lactation decreased the neurotropic development of neurons formed at the embryo stage (e12.5) and impaired early postnatal neurogenesis in the hypothalamic regions of both males and females. Males show a larger increased ratio of Neuropeptide Y (NPY) to Pro-opiomelanocortin (POMC) neurons in early postnatal neurogenesis, in response to maternal HFD, setting an obese tone for male offspring. These data provide insights into the mechanisms by which hypothalamic reprograming by early life overnutrition contributes to the sex-dependent susceptibility to obesity in adult life in mice.
早期生活营养可以重新编程发育,并对体重调节产生长期影响。在小鼠中,哺乳期的母体高脂肪饮食(HFD)使雄性后代而非雌性后代在成年后易患饮食诱导的肥胖。在早期产后生活中,在与母体饮食有关的重要时间点检查了下丘脑的分子和细胞变化,并证明了下丘脑的性别差异重新编程。哺乳期的母体 HFD 减少了在胚胎阶段(e12.5)形成的神经元的神经营养发育,并损害了雄性和雌性下丘脑区域的早期产后神经发生。雄性在早期产后神经发生中显示出更多的神经肽 Y(NPY)到促黑皮质素原(POMC)神经元的增加比例,以响应母体 HFD,为雄性后代设定肥胖基调。这些数据提供了有关早期生活营养过度重塑下丘脑如何导致小鼠成年后肥胖易感性的性别依赖性的机制的见解。