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Maternal resveratrol intake during lactation attenuates hepatic triglyceride and fatty acid synthesis in adult male rat offspring

机译:哺乳期母体白藜芦醇的摄入会减弱成年雄性大鼠后代的肝甘油三酸酯和脂肪酸合成

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Resveratrol (3,5,4-trihydroxystilbene) is a natural polyphenolic compound found in grapes and red wine and has been shown to exert protective effects on the liver preventing lipid accumulation induced by a high-fat diet. However, no studies have shown that the nutritional resveratrol intake by the parental generation has modified lipogenesis in an adult offspring. The aim of this study was to investigate whether maternal resveratrol intake during lactation affects lipogenesis in adult male rat offspring, and if it does, what is the molecular mechanistic basis. Six male pups born from mothers given a control diets during lactation (CC group) and six male pups born from mothers given a control diet as well as resveratrol during lactation (CR group) were fed a standard diet until sacrifice at 36 weeks. Adult male offspring from mothers given resveratrol during lactation (CR group) had lower body weight from the fourth week of lactation until adulthood, but no significant change was observed in the relative food intake. Low levels of plasma triacylglycerol were found in the CR group compared to the CC group. Histopathological analysis of the livers of adult male rat offspring revealed lipid accumulation in hepatocytes in the CC group, whereas lipid droplets were rare in the CR group. Hepatic protein levels of AMPK-phosphorylated at ser403, Sirt1, and Nampt in the CR group were upregulated significantly compared to the CC group. These results indicated the maternal resveratrol intake during lactation-induced activation of AMPK through Sirt1 upregulation. In this study, significant upregulation of the levels of precursor of sterol regulatory element binding protein-1c (SREBP-1c) and downregulation of the ratio of active-SREBP-1c/precusor-SREBP-1c were observed in the CR group compared to the CC group. These results suggested that proteolytic processing of SREBP-1c was suppressed by AMPK in the livers of the CR group. It is well known that SREBP-1c regulates the lipogenic pathway by activating genes involved in triglyceride and fatty acid synthesis. The present study showed significant downregulation of hepatic fatty acid synthase (FAS) and acetyl-CoA carboxylase (ACC) levels in the CR group. These results indicated that maternal resveratrol intake during lactation suppressed SREBP-1c cleavage and nuclear translocation and repressed SREBP-1c target gene expression such as FAS and ACC in the livers of adult male offspring. These changes attenuate hepatic triacylglycerol and fatty acid synthesis in adult male offspring. Highlights ? Maternal resveratrol intake during lactation attenuates hepatic triglyceride and fatty acid synthesis in adult male rat offspring. ? Maternal resveratrol intake during lactation induces the activation of AMPK through Sirt1 upregulation in the livers of adult male rat offspring. ? Maternal resveratrol intake during lactation suppressed the proteolytic processing of SREBP-1c and SREBP-1c target gene expression, such as FAS and ACC, in the livers of adult male rat offspring.
机译:白藜芦醇(3,5,4-三羟基sti)是一种天然的多酚化合物,存在于葡萄和红酒中,已显示出对肝脏的保护作用,可防止高脂饮食诱导的脂质蓄积。但是,没有研究表明,父母代摄入的营养白藜芦醇可以改善成年后代的脂肪生成。这项研究的目的是调查哺乳期母体白藜芦醇的摄入是否会影响成年雄性大鼠后代的脂肪生成,如果确实如此,其分子机理是什么。对六只从母乳喂养的母亲幼崽(CC组)和六只从母乳喂养的母亲幼崽以及白藜芦醇(泌乳组)进行标准饮食直至在第36周处死。从哺乳期给予白藜芦醇的母亲的成年男性后代(CR组)从哺乳第四周到成年期体重较低,但相对食物摄入量未见明显变化。与CC组相比,CR组血浆三酰甘油水平较低。对成年雄性大鼠后代肝脏的组织病理学分析显示,CC组肝细胞中脂质蓄积,而CR组中脂质滴少见。与CC组相比,CR组的Ser403,Sirt1和Nampt磷酸化的AMPK的肝蛋白水平显着上调。这些结果表明在哺乳期通过Sirt1上调激活的AMPK激活期间母体摄取白藜芦醇。在这项研究中,与对照组相比,CR组的固醇调节元件结合蛋白-1c(SREBP-1c)前体水平显着上调,而活性-SREBP-1c / precusor-SREBP-1c的比例下调。 CC组。这些结果表明,CR组肝脏中AMPK抑制了SREBP-1c的蛋白水解过程。众所周知,SREBP-1c通过激活参与甘油三酸酯和脂肪酸合成的基因来调节脂肪生成途径。本研究显示CR组的肝脏脂肪酸合酶(FAS)和乙酰辅酶A羧化酶(ACC)水平显着下调。这些结果表明,哺乳期母体摄入白藜芦醇可抑制成年男性后代肝脏中的SREBP-1c裂解和核易位,并抑制SREBP-1c靶基因表达,如FAS和ACC。这些变化减弱了成年雄性后代的肝三酰甘油和脂肪酸合成。强调 ?哺乳期母体白藜芦醇的摄入会减弱成年雄性大鼠后代的肝甘油三酸酯和脂肪酸合成。 ?哺乳期母体摄入白藜芦醇可通过Sirt1上调在成年雄性大鼠后代的肝脏中诱导AMPK的激活。 ?哺乳期母体摄入白藜芦醇可抑制成年雄性大鼠后代肝脏中SREBP-1c和SREBP-1c目标基因表达(例如FAS和ACC)的蛋白水解过程。

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