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Maternal Food Restriction during Pregnancy and Lactation Adversely Affect Hepatic Growth and Lipid Metabolism in Three-Week-Old Rat Offspring

机译:孕期和哺乳期的母体食物限制不利地影响三周龄大鼠后代的肝生长和脂质代谢

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摘要

Maternal malnutrition influences the early development of foetal adaptive changes for survival. We explored the effects of maternal undernutrition during gestation and lactation on hepatic growth and function. Sprague-Dawley rats were fed a normal or a food-restricted (FR) diet during gestation and/or lactation. We performed analyses of covariance (adjusting for the liver weight/body weight ratio) to compare hepatic growth and lipid metabolism among the offspring. Maternal FR during gestation triggered the development of wide spaces between hepatic cells and increased the expression of mammalian target of rapamycin (mTOR) in three-week-old male offspring compared with controls (both p < 0.05). Offspring nursed by FR dams exhibited wider spaces between hepatic cells and a lower liver weight/body weight ratio than control offspring, and increased mTOR expression (p < 0.05). Interestingly, the significant decrease in expression of lipogenic-related genes was dependent on carbohydrate-responsive element-binding protein, despite the increased expression of sterol regulatory element-binding protein 1 (SREBP1) (p < 0.05). This study demonstrated increased expression of key metabolic regulators (mTOR and SREBP1), alterations in lipid metabolism, and deficits in hepatic growth in the offspring of FR-treated dams.
机译:产妇营养不良影响胎儿生存适应性改变的早期发展。我们探讨了孕期和哺乳期母亲营养不良对肝生长和功能的影响。在妊娠和/或哺乳期间,给Sprague-Dawley大鼠喂食正常或食物限制(FR)饮食。我们进行了协方差分析(调整了肝脏的重量/体重比),以比较子代之间的肝生长和脂质代谢。与对照组相比,孕期孕产妇FR在三周大的雄性后代中触发了肝细胞之间宽阔空间的发展,并增加了雷帕霉素(mTOR)哺乳动物靶标的表达(均p <0.05)。与对照后代相比,FR大坝育成的后代在肝细胞之间显示出更宽的空间,肝脏重量/体重比更低,并且mTOR表达增加(p <0.05)。有趣的是,尽管固醇调节元件结合蛋白1(SREBP1)的表达增加,但脂肪生成相关基因的表达显着下降取决于碳水化合物反应性元件结合蛋白(p <0.05)。这项研究表明,FR处理水坝后代中主要的代谢调节因子(mTOR和SREBP1)的表达增加,脂质代谢的改变以及肝生长的缺陷。

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