Danone Nutricia Research, Utrecht, 3584 CT, The Netherlands.
Human and Animal Physiology, Wageningen University, Wageningen, 6708 WD, The Netherlands.
Mol Nutr Food Res. 2024 Jan;68(1):e2300470. doi: 10.1002/mnfr.202300470. Epub 2023 Nov 20.
Human milk (HM) is considered optimal nutrition for infants, beneficially programming adult health outcomes including reduced obesity risk. Early life exposure to infant formula with lipid droplets closely resembling the structural properties of HM lipid globules (Nuturis) attenuated white adipose tissue (WAT) accumulation in mice upon adult western-style diet (WSD) feeding. Here, the study aims to elucidate underlying mechanisms.
Mice are raised on control or Nuturis diets between postnatal days 16-42 followed by either standard diet or WSD for 16 weeks. While the adult body composition of mice on a standard diet is not significantly affected, Nuturis reduced adiposity in mice on WSD. Morphologically, mean adipocyte size is reduced in Nuturis-raised mice, independent of adult diet exposure, and WAT macrophage content is reduced, albeit not significantly. Transcriptomics of epididymal WAT indicate potential beneficial effects on energy metabolism and macrophage function by Nuturis.
Reduced adult adiposity by early life exposure to Nuturis appears to be associated with smaller adipocytes and alterations in WAT immune and energy metabolism. These results suggest that early modulation of WAT structure and/or function may contribute to the protective programming effects of the early-life Nuturis diet on later-life adiposity.
人乳被认为是婴儿的最佳营养来源,有益于成年后健康结果的编程,包括降低肥胖风险。在生命早期接触到与人乳脂肪球结构特性非常相似的脂质体的婴儿配方奶粉(Nuturis),可减轻成年西式饮食(WSD)喂养的小鼠的白色脂肪组织(WAT)积累。本研究旨在阐明其潜在机制。
在出生后第 16-42 天,将小鼠分别用对照或 Nuturis 饮食饲养,然后用标准饮食或 WSD 喂养 16 周。虽然标准饮食的成年小鼠的身体成分没有显著影响,但 Nuturis 降低了 WSD 小鼠的肥胖程度。形态学上,Nuturis 喂养的小鼠的平均脂肪细胞大小减小,与成年饮食暴露无关,且 WAT 巨噬细胞含量减少,但无统计学意义。附睾 WAT 的转录组学表明,Nuturis 对能量代谢和巨噬细胞功能具有潜在的有益影响。
生命早期接触 Nuturis 降低了成年肥胖的程度,这似乎与人乳脂肪球结构特性非常相似,与较小的脂肪细胞和 WAT 免疫及能量代谢的改变有关。这些结果表明,早期调节 WAT 的结构和/或功能可能有助于早期生命 Nuturis 饮食对后期肥胖的保护编程作用。