首页> 外文期刊>The British Journal of Nutrition >Intra-uterine undernutrition amplifies age-associated glucose intolerance in pigs via altered DNA methylation at muscle GLUT4 promoter
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Intra-uterine undernutrition amplifies age-associated glucose intolerance in pigs via altered DNA methylation at muscle GLUT4 promoter

机译:子宫内营养不良会通过改变肌肉GLUT4启动子的DNA甲基化来放大猪的年龄相关葡萄糖不耐症

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The present study aimed to investigate the effect of maternal malnutrition on offspring glucose tolerance and the epigenetic mechanisms involved. In total, twelve primiparous Landrace x Yorkshire gilts were fed rations providing either 100% (control (CON)) or 75% (undernutrition (UN)) nutritional requirements according to the National Research Council recommendations, throughout gestation. Muscle samples of offspring were collected at birth (dpn1), weaning (dpn28) and adulthood (dpn189). Compared with CON pigs, UN pigs showed lower serum glucose concentrations at birth, but showed higher serum glucose and insulin concentrations as well as increased area under the blood glucose curve during intravenous glucose tolerance test at dpn189 (P 0.05). Compared with CON pigs, GLUT-4 gene and protein expressions were decreased at dpn1 and dpn189 in the muscle of UN pigs, which was accompanied by increased methylation at the GLUT4 promoter (P0.05). These alterations in methylation concurred with increased mRNA levels of DNA methyltransferase (DNMT) 1 at dpn1 and dpn28, DNMT3a at dpn189 and DNMT3b at dpn1 in UN pigs compared with CON pigs (P 0.05). Interestingly, although the average methylation levels at the muscle GLUT4 promoter were decreased at dpn189 compared with dpn1 in pigs exposed to a poor maternal diet (P 0.05), the methylation differences in individual CpG sites were more pronounced with age. Our results indicate that in utero undernutrition persists to silence muscle GLUT4 likely through DNA methylation during the ageing process, which may lead to the amplification of age-associated glucose intolerance.
机译:本研究旨在调查孕产妇营养不良对后代葡萄糖耐量的影响及其所涉及的表观遗传机制。根据国家研究委员会的建议,在整个妊娠期间,总共喂食了十二头初生长白x约克夏小母猪,提供100%(对照(CON))或75%(营养不良(UN))的营养需求。在出生(dpn1),断奶(dpn28)和成年(dpn189)时采集后代的肌肉样本。与CON猪相比,UN猪出生时显示较低的血糖浓度,但在dpn189静脉葡萄糖耐量试验期间显示较高的血糖和胰岛素浓度,以及血糖曲线下的面积增加(P <0.05)。与CON猪相比,UN猪肌肉中dpn1和dpn189的GLUT-4基因和蛋白表达降低,同时在GLUT4启动子处甲基化增加(P <0.05)。与CON猪相比,这些甲基化改变与联合国猪相比,dpn1和dpn28处的DNA甲基转移酶(DNMT)1,dpn189处的DNMT3a和dpn1处的DNMT3b mRNA水平升高(P <0.05)。有趣的是,尽管暴露于不良母体饮食的猪中,dpn189肌肉GLUT4启动子的平均甲基化水平比dpn1降低(P <0.05),但各个CpG位点的甲基化差异随年龄增长更为明显。我们的结果表明,在子宫内营养不良持续存在,可能通过衰老过程中的DNA甲基化使肌肉GLUT4沉默,这可能导致与年龄相关的葡萄糖耐量增加。

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