Institute of Human Nutrition and Food Science, Molecular Prevention, Christian-Albrechts-University of Kiel, Kiel, Germany.
Mol Nutr Food Res. 2013 Feb;57(2):277-90. doi: 10.1002/mnfr.201200315. Epub 2012 Nov 29.
Epidemiological and experimental evidence indicates that maternal nutrition status contributes to long-term changes in the metabolic phenotype of the offspring, a process known as fetal programming.
We have used a swine model (Sus scrofa) to analyze consequences of a maternal low protein diet (about 50% of control) during pregnancy on hepatic lipid metabolism and genome-wide hepatic gene expression profile of juvenile female offspring (mean age 85 days). We found 318 S. scrofa genes to be differentially expressed in the liver at age 85 days. In the low protein offspring group key genes of fatty acid de novo synthesis were downregulated whereas several genes of lipolysis and phospholipid biosynthesis were upregulated. qRT-PCR analysis of selected genes verified microarray data and revealed linear correlations between gene expression levels and slaughter weight. Hepatic cholesterol 7α hydroxylase protein expression tended to be lower in the low protein group. Total lipid and triglyceride content and fatty acid composition of total lipids were not different between groups.
A maternal low protein diet during pregnancy induces a distinct hepatic gene expression signature in juvenile female pigs which was not translated into phenotypical changes of liver lipid metabolism.
流行病学和实验证据表明,母体营养状况有助于后代代谢表型的长期变化,这一过程被称为胎儿编程。
我们使用猪模型(Sus scrofa)分析了妊娠期间母体低蛋白饮食(约为对照组的 50%)对未成年雌性后代(平均年龄 85 天)肝脏脂质代谢和全基因组肝脏基因表达谱的影响。我们发现 318 个 S. scrofa 基因在 85 天时在肝脏中表达差异。在低蛋白后代组中,脂肪酸从头合成的关键基因下调,而脂肪分解和磷脂生物合成的几个基因上调。所选基因的 qRT-PCR 分析验证了微阵列数据,并显示基因表达水平与屠宰体重之间存在线性相关性。低蛋白组中肝胆固醇 7α羟化酶蛋白表达趋于降低。两组间总脂质和甘油三酯含量以及总脂质的脂肪酸组成无差异。
妊娠期间母体低蛋白饮食会在未成年雌性猪的肝脏中诱导出明显的基因表达特征,但并未转化为肝脏脂质代谢的表型变化。