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哺乳期母体摄入白藜芦醇可减轻成年雄性大鼠后代肝脏甘油三酯和脂肪酸的合成。

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

作者信息

Tanaka Masato, Kita Tomomi, Yamasaki Shojiro, Kawahara Tae, Ueno Yukako, Yamada Mai, Mukai Yuuka, Sato Shin, Kurasaki Masaaki, Saito Takeshi

机构信息

Graduate School of Health Sciences, Hokkaido University, Sapporo, Japan.

School of Nutrition and Dietetics, Faculty of Health and Social Work, Kanagawa University of Human Services, Kanagawa, Japan.

出版信息

Biochem Biophys Rep. 2017 Jan 5;9:173-179. doi: 10.1016/j.bbrep.2016.12.011. eCollection 2017 Mar.

DOI:10.1016/j.bbrep.2016.12.011
PMID:28956002
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5614589/
Abstract

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.

摘要

白藜芦醇(3,5,4 - 三羟基茋)是一种存在于葡萄和红酒中的天然多酚化合物,已被证明对肝脏具有保护作用,可防止高脂饮食诱导的脂质积累。然而,尚无研究表明亲代摄入白藜芦醇会改变成年子代的脂肪生成。本研究的目的是调查哺乳期母体摄入白藜芦醇是否会影响成年雄性大鼠子代的脂肪生成,如果有影响,其分子机制基础是什么。六只哺乳期母亲给予对照饮食的雄性幼崽(CC组)和六只哺乳期母亲给予对照饮食及白藜芦醇的雄性幼崽(CR组)被喂食标准饮食,直至36周时处死。哺乳期母亲给予白藜芦醇的成年雄性子代(CR组)从哺乳期第四周直至成年体重较低,但相对食物摄入量未观察到显著变化。与CC组相比,CR组血浆三酰甘油水平较低。成年雄性大鼠子代肝脏的组织病理学分析显示,CC组肝细胞中有脂质积累,而CR组脂质滴很少见。与CC组相比,CR组中丝氨酸403位点磷酸化的AMPK、Sirt1和Nampt的肝脏蛋白水平显著上调。这些结果表明哺乳期母体摄入白藜芦醇通过上调Sirt1诱导AMPK激活。在本研究中,与CC组相比,CR组中固醇调节元件结合蛋白-1c(SREBP-1c)前体水平显著上调,活性-SREBP-1c/前体-SREBP-1c比值下调。这些结果表明CR组肝脏中SREBP-1c的蛋白水解加工受到AMPK抑制。众所周知,SREBP-1c通过激活参与甘油三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组肝脏中脂肪酸合酶(FAS)和乙酰辅酶A羧化酶(ACC)水平显著下调。这些结果表明哺乳期母体摄入白藜芦醇抑制了成年雄性子代肝脏中SREBP-1c的切割和核转位,并抑制了SREBP-1c靶基因如FAS和ACC的表达。这些变化减弱了成年雄性子代肝脏中三酰甘油和脂肪酸的合成。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/75d0/5614589/46288544823b/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/75d0/5614589/9f1d267b1413/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/75d0/5614589/e1081170da84/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/75d0/5614589/8711725d31d7/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/75d0/5614589/8908a5e61ee0/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/75d0/5614589/951acd0e75c3/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/75d0/5614589/46288544823b/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/75d0/5614589/9f1d267b1413/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/75d0/5614589/e1081170da84/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/75d0/5614589/8711725d31d7/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/75d0/5614589/8908a5e61ee0/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/75d0/5614589/951acd0e75c3/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/75d0/5614589/46288544823b/gr6.jpg

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