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首页> 外文期刊>The Journal of Nutritional Biochemistry >Postnatal exposure to a high-carbohydrate diet interferes epigenetically with thyroid hormone receptor induction of the adult male rat skeletal muscle glucose transporter isoform 4 expression
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Postnatal exposure to a high-carbohydrate diet interferes epigenetically with thyroid hormone receptor induction of the adult male rat skeletal muscle glucose transporter isoform 4 expression

机译:出生后暴露于高碳水化合物饮食会成年后干扰成年雄性大鼠骨骼肌葡萄糖转运蛋白亚型4表达的甲状腺激素受体诱导

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摘要

Early life nutritional intervention causes adult-onset insulin resistance and obesity in rats. Thyroid hormone receptor (TR), in turn, transcriptionally enhances skeletal muscle Glut4 expression. We tested the hypothesis that reduced circulating thyroid-stimulating hormone and T4 concentrations encountered in postnatal (PN4-PN24) high-carbohydrate (HC) milk formula-fed versus the mother-fed controls (MF) would epigenetically interfere with TR induction of adult (100 days) male rat skeletal muscle Glut4 expression, thereby providing a molecular mechanism mediating insulin resistance. We observed increased DNA methylation of the CpG island with enhanced recruitment of Dnmt3a, Dnmt3b and MeCP2 in the glut4 promoter region along with reduced acetylation of histone (H)2A.Z and H4 particularly at the H4.lysine (K)16 residue, which was predominantly mediated by histone deacetylase 4 (HDAC4). This was followed by enhanced recruitment of heterochromatin protein 1 beta to the glut4 promoter with increased Suv39H1 methylase concentrations. These changes reduced TR binding of the T3 response element of the glut4 gene (TREs; 473 to 450 bp) detected qualitatively in vivo (electromobility shift assay) and quantified ex vivo (chromatin immunoprecipitation). In addition, the recruitment of steroid receptor coactivator and CREB-binding protein to the glut4 promoter-protein complex was reduced. Co-immunoprecipitation experiments confirmed the interaction between TR and CBP to be reduced and HDAC4 to be enhanced in HC versus MF groups. These molecular changes were associated with diminished skeletal muscle Glut4 mRNA and protein concentrations. We conclude that early postnatal exposure to HC diet epigenetically reduced TR induction of adult male skeletal muscle Glut4 expression, uncovering novel molecular mechanisms contributing to adult insulin resistance and obesity. (C) 2014 Published by Elsevier Inc.
机译:生命早期的营养干预会导致成年大鼠胰岛素抵抗和肥胖。甲状腺激素受体(TR)进而通过转录增强骨骼肌Glut4的表达。我们检验了以下假设:在配方奶喂养的产后(PN4-PN24)高碳水化合物(HC)的牛奶中,与母亲喂养的对照(MF)相比,循环甲状腺刺激激素和T4浓度降低会从表观上影响成人的TR诱导( 100天)雄性大鼠骨骼肌Glut4表达,从而提供介导胰岛素抵抗的分子机制。我们观察到CpG岛的DNA甲基化增加,而glut4启动子区域中Dnmt3a,Dnmt3b和MeCP2的募集增加,同时组蛋白(H)2A.Z和H4的乙酰化程度降低,尤其是在H4。赖氨酸(K)16残基上,这主要由组蛋白脱乙酰基酶4(HDAC4)介导。随后,随着Suv39H1甲基化酶浓度的增加,异染色质蛋白1β增强了向glut4启动子的募集。这些变化降低了在体内定性检测(电迁移率测定)和定量离体(染色质免疫沉淀)的glut4基因的T3反应元件(TRE; 473至450 bp)的TR结合。另外,减少了将类固醇受体共激活剂和CREB结合蛋白募集到glut4启动子-蛋白复合物中。免疫共沉淀实验证实,HC组和MF组的TR和CBP之间的相互作用减少,HDAC4增强。这些分子变化与骨骼肌Glut4 mRNA和蛋白质浓度降低有关。我们得出的结论是,出生后早期接触HC饮食在表观遗传上减少了成年男性骨骼肌Glut4表达的TR诱导,揭示了导致成年胰岛素抵抗和肥胖症的新型分子机制。 (C)2014由Elsevier Inc.发行

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