Research Center, Dr. von Hauner Children's Hospital, Ludwig-Maximilians-Universität München, Lindwurmstrasse 4, 80337 Munich, Germany.
German Mouse Clinic, Institute of Experimental Genetics, Helmholtz Zentrum München, Ingolstädter Landstrasse 1, 85764 Neuherberg, Germany; German Center for Diabetes Research (DZD), Ingolstädter Landstrasse 1, 85764 Neuherberg, Germany.
Biochim Biophys Acta Mol Basis Dis. 2017 Jun;1863(6):1605-1614. doi: 10.1016/j.bbadis.2017.02.021. Epub 2017 Feb 21.
Peri-conceptional exposure to maternal obesogenic nutrition is associated with in utero programming of later-life overweight and metabolic disease in the offspring. We aimed to investigate whether dietary intervention with a modified fatty acid quality in an obesogenic high-calorie (HC) diet during the preconception and gestational phases can improve unfavourable effects of an adipogenic maternal environment. In NMRI mice, peri-conceptional and gestational obesity was induced by feeding a HC diet (controls), and they were compared with dams on a fat-modified (Fat-mod) HC diet of the same energy content but enriched with medium-chain fatty acids (MCFAs) and adjusted to a decreased ratio of n-6 to n-3 long-chain polyunsaturated fatty acids (LC-PUFAs). Effects on maternal and placental outcomes at delivery (day 17.5 post coitum) were investigated. Despite comparable energy assimilation between the two groups of dams, the altered fatty acid composition of the Fat-mod HC diet induced lower maternal body weight, weights of fat depots, adipocyte size, and hepatic fat accumulation compared to the unmodified HC diet group. Further, there was a trend towards lower fasting glucose, insulin and leptin concentrations in dams fed the Fat-mod HC diet. Phenotypic changes were accompanied by inhibition of transcript and protein expression of genes involved in hepatic de novo lipogenesis comprising PPARG2 and its target genes Fasn, Acaca, and Fabp4, whereas regulation of other lipogenic factors (Srebf1, Nr1h3, Abca1) appeared to be more complex. The modified diet led to a sex-specific placental response by upregulating PPARG-dependent fatty acid transport gene expression in female versus male placentae. Qualitative modification of the fatty acid spectrum of a high-energy maternal diet, using a combination of both MCFAs and n-3 LC-PUFAs, seems to be a promising interventional approach to ameliorate the adipogenic milieu of mice before and during gestation.
孕前接触母体肥胖相关营养与后代宫内编程后半生超重和代谢性疾病有关。我们旨在研究在孕前和妊娠期,用改良脂肪酸质量的饮食干预肥胖高热量(HC)饮食是否可以改善肥胖母体环境的不利影响。在 NMRI 小鼠中,通过喂饲高热量 HC 饮食(对照组)诱导孕前和妊娠期肥胖,并将其与高脂肪修饰(Fat-mod)HC 饮食的母鼠进行比较,后者具有相同的能量含量,但富含中链脂肪酸(MCFAs),并调整为 n-6 与 n-3 长链多不饱和脂肪酸(LC-PUFAs)的比例降低。研究了分娩时(妊娠后 17.5 天)母代和胎盘结局的影响。尽管两组母鼠的能量吸收相当,但 Fat-mod HC 饮食中改变的脂肪酸组成导致母鼠体重、脂肪沉积重量、脂肪细胞大小和肝脂肪堆积低于未修饰的 HC 饮食组。此外,饲喂 Fat-mod HC 饮食的母鼠空腹血糖、胰岛素和瘦素浓度呈下降趋势。表型变化伴随着肝从头脂肪生成相关基因的转录和蛋白表达受到抑制,包括 PPARG2 及其靶基因 Fasn、Acaca 和 Fabp4,而其他脂生成因子(Srebf1、Nr1h3、Abca1)的调节似乎更为复杂。该改良饮食通过上调 PPARG 依赖性脂肪酸转运基因在雌性而非雄性胎盘中的表达,导致了胎盘的性别特异性反应。用 MCFAs 和 n-3 LC-PUFAs 的组合对高能量母体饮食的脂肪酸谱进行定性修饰,似乎是一种有前途的干预方法,可以改善妊娠前和妊娠期间的小鼠肥胖环境。