Elahi Maqsood M, Cagampang Felino R, Mukhtar Dhea, Anthony Frederick W, Ohri Sunil K, Hanson Mark A
Institute of Developmental Sciences, Developmental Origins of Health and Disease Division, University of Southampton School of Medicine, Southampton General Hospital, Mailpoint 887, Southampton SO16 6YD, UK.
Br J Nutr. 2009 Aug;102(4):514-9. doi: 10.1017/S000711450820749X. Epub 2009 Feb 10.
In rodents, adverse prenatal nutrition, such as a maternal diet rich in fat during pregnancy, enhances susceptibility of the offspring to hypertension, type 2 diabetes and other features of the human metabolic syndrome in adulthood. However, previous experimental studies were confined to short-term modifications of the maternal diet during pregnancy and/or lactation periods, a situation uncommon in humans. Moreover in humans, the offspring may also consume a high-fat diet, which may take them beyond the range to which their development has adapted them to respond healthily. We examined in C57 mice the effects on offspring of feeding their mothers a high-fat (HF) or standard chow (C) diet from weaning through pregnancy and lactation, and whether there are additive phenotypic effects of feeding the offspring an HF diet from weaning to adulthood (dam-offspring dietary group HF-HF). This group was compared with offspring from HF-fed dams fed a C diet from weaning to adulthood (HF-C) and offspring from C-fed mothers fed the C or HF diet (C-C and HF-C, respectively). HF-HF, HF-C and C-HF adult female offspring were heavier, fatter, and had raised serum cholesterol and blood pressure compared with C-C female offspring. We observed a similar trend in male offspring except for the HF-C group which was not heavier or fatter than male C-C offspring. Histology showed lipid vacuoles within hepatocytes in the HF-HF, HF-C and C-HF but not the CC offspring. Serum C-reactive protein was elevated in female (C-HF and HF-HF) but not in male offspring. Elevated blood pressure in the HF-C and C-HF groups was attenuated in the HF-HF group in males but not in females. These findings indicate that long-term consumption of an HF diet by the mother predisposes her offspring to developing a metabolic syndrome-like phenotype in adult life, although cardiovascular effects of an HF diet are related to sex specificity in the HF-HF group.
在啮齿动物中,产前不良营养,如孕期母体富含脂肪的饮食,会增加后代成年后患高血压、2型糖尿病及人类代谢综合征其他特征的易感性。然而,以往的实验研究局限于孕期和/或哺乳期对母体饮食的短期改变,这种情况在人类中并不常见。此外,在人类中,后代也可能食用高脂肪饮食,这可能使他们超出其发育所适应的健康反应范围。我们在C57小鼠中研究了从断奶到怀孕及哺乳期给母鼠喂食高脂肪(HF)或标准饲料(C)对后代的影响,以及从断奶到成年给后代喂食HF饮食是否存在累加表型效应(母-后代饮食组HF-HF)。将该组与断奶到成年喂食C饮食的HF母鼠后代(HF-C)以及喂食C或HF饮食的C饮食母鼠后代(分别为C-C和C-HF)进行比较。与C-C雌性后代相比,HF-HF、HF-C和C-HF成年雌性后代更重、更胖,血清胆固醇和血压升高。我们在雄性后代中观察到类似趋势,但HF-C组雄性后代不比C-C雄性后代更重或更胖。组织学显示,HF-HF、HF-C和C-HF组肝细胞内有脂质空泡,而C-C后代没有。雌性(C-HF和HF-HF)后代血清C反应蛋白升高,雄性后代则未升高。HF-C和C-HF组升高的血压在雄性HF-HF组中减弱,但在雌性中未减弱。这些发现表明,母亲长期食用HF饮食会使其后代在成年后易患代谢综合征样表型,尽管HF饮食的心血管影响在HF-HF组中与性别特异性有关。