Faculty of Health and Medical Sciences, Department of Veterinary Clinical and Animal Sciences, University of Copenhagen, Frederiksberg, Denmark; Centre for Fetal Programming, Copenhagen, Denmark.
Acta Physiol (Oxf). 2014 Feb;210(2):317-29. doi: 10.1111/apha.12211. Epub 2013 Dec 27.
Determine the impacts of pre- and early-post-natal nutrition on selected markers of hepatic glucose and fat metabolism.
Twin-bearing ewes were fed 100% (NORM) or 50% (LOW) of protein and energy requirements during the last 6-weeks of gestation. Twin-lambs received either a high-carbohydrate high-fat (HCHF) or conventional (CONV) diet from 3 days to 6 months of age (around puberty), whereafter lambs from the four subgroups were slaughtered (16 males/3 females). Remaining lambs (19 females) were fed a moderate diet and slaughtered at 2 years of age (young adults).
Pre-natal LOW nutrition was associated with increased hepatic triglyceride, ceramide and free fatty acid content in adulthood (not observed in lambs), which was accompanied by up-regulated early-stage insulin signalling as reflected by increased INSRβ and PI3K-p110 protein expression. The HCHF diet increased hepatic triglyceride content in lambs, associated with down-regulated expressions of energy-metabolism-related genes (GLUT1, PPARα, SREBP1c, PEPCK). These post-natal effects were not observed in adult HCHF sheep, after they had received a moderate (body-fat correcting) diet for 1.5 years. Interestingly, pre-natal LOW nutrition induced permanent alterations in hepatic phospholipids' fatty acid composition. Thus, the amount of linoleic acid (C18 : 2 ∆(9,12)) was significantly increased and composition of rumen-derived fatty acids were altered, indicating changed composition of rumenal microbiota.
Hepatic insulin signalling and linoleic and microbial-derived fatty acid content in phospholipids are targets of foetal programming induced by late-gestation undernutrition. Future studies are required to explain their cause-effect associations with increased risks of developing hepatic steatosis and insulin insensitivity in adulthood.
确定产前和产后营养对肝脏葡萄糖和脂肪代谢相关标志物的影响。
在妊娠的最后 6 周内,双胎妊娠母羊分别接受 100%(NORM)或 50%(LOW)的蛋白质和能量需求喂养。双胎羔羊在出生后 3 天至 6 个月(青春期左右)期间分别接受高碳水化合物高脂肪(HCHF)或常规(CONV)饮食,此后,4 个亚组的羔羊被屠宰(16 只雄性/3 只雌性)。其余羔羊(19 只雌性)喂食中等饮食,并在 2 岁时屠宰(成年早期)。
产前 LOW 营养与成年后肝脏甘油三酯、神经酰胺和游离脂肪酸含量增加有关(在羔羊中未观察到),这伴随着早期胰岛素信号的上调,表现为 INSRβ 和 PI3K-p110 蛋白表达增加。HCHF 饮食增加了羔羊肝脏中的甘油三酯含量,与能量代谢相关基因(GLUT1、PPARα、SREBP1c、PEPCK)的下调表达有关。在 HCHF 绵羊接受 1.5 年中等(体脂纠正)饮食后,这些产后影响在成年 HCHF 羊中并未观察到。有趣的是,产前 LOW 营养导致肝脏磷脂脂肪酸组成发生永久性改变。因此,亚油酸(C18:2 ∆(9,12))的含量显著增加,瘤胃衍生脂肪酸的组成发生改变,表明瘤胃微生物群组成发生改变。
肝脏胰岛素信号和磷脂中 linoleic 及微生物衍生脂肪酸含量是晚期妊娠营养不良诱导的胎儿编程的靶点。需要进一步的研究来解释它们与成年期发生肝脂肪变性和胰岛素不敏感风险增加的因果关系。