首页> 美国卫生研究院文献>Nutrients >n-3 Polyunsaturated Fatty Acids Decrease Long-Term Diabetic Risk of Offspring of Gestational Diabetes Rats by Postponing Shortening of Hepatic Telomeres and Modulating Liver Metabolism
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n-3 Polyunsaturated Fatty Acids Decrease Long-Term Diabetic Risk of Offspring of Gestational Diabetes Rats by Postponing Shortening of Hepatic Telomeres and Modulating Liver Metabolism

机译:n-3多不饱和脂肪酸通过延迟肝端粒的缩短和调节肝脏代谢来降低妊娠糖尿病大鼠后代的长期糖尿病风险

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摘要

The long-term influence of gestational diabetes mellitus (GDM) on offspring and the effect of omega-3 polyunsaturated fatty acids (n-3 PUFA) on GDM offspring are poorly understood. We studied the long-term diabetic risk in GDM offspring and evaluated the effect of n-3 PUFA intervention. Healthy offspring rats were fed standard diet (soybean oil) after weaning. GDM offspring were divided into three groups: GDM offspring (soybean oil), n-3 PUFA adequate offspring (fish oil), and n-3 PUFA deficient offspring (safflower oil), fed up to 11 months old. The diabetic risk of GDM offspring gradually increased from no change at weaning to obvious impaired glucose and insulin tolerance at 11 months old. n-3 PUFA decreased oxidative stress and inflammation in the liver of older GDM offspring. There was a differential effect of n-3 PUFA and n-6 PUFA on hepatic telomere length in GDM offspring. Non-targeted metabolomics showed that n-3 PUFA played a modulating role in the liver, in which numerous metabolites and metabolic pathways were altered when GDM offspring grew to old age. Many metabolites were related to diabetes risk, such as α-linolenic acid, palmitic acid, ceramide, oxaloacetic acid, tocotrienol, tetrahydro-11-deoxycortisol, andniacinamide. In summary, GDM offspring exhibited obvious diabetes risk at old age, whereas n-3 PUFA decreased this risk.
机译:妊娠糖尿病(GDM)对后代的长期影响以及Omega-3多不饱和脂肪酸(n-3 PUFA)对GDM后代的影响知之甚少。我们研究了GDM后代的长期糖尿病风险,并评估了n-3 PUFA干预的效果。断奶后给健康的后代大鼠喂食标准饮食(大豆油)。 GDM后代分为三组:喂食至11个月大的GDM后代(大豆油),n-3 PUFA充足的后代(鱼油)和n-3 PUFA缺乏后代(红花油)。 GDM后代的糖尿病风险从断奶时无变化逐渐增加到11个月大时葡萄糖和胰岛素耐受性明显受损。 n-3 PUFA降低了老​​年GDM后代肝脏的氧化应激和炎症。在GDM后代中,n-3 PUFA和n-6 PUFA对肝端粒长度有不同的影响。非靶向代谢组学表明,n-3 PUFA在肝脏中起调节作用,当GDM后代长大时,其中许多代谢物和代谢途径发生了改变。许多代谢物与糖尿病风险有关,例如α-亚麻酸,棕榈酸,神经酰胺,草酰乙酸,生育三烯酚,四氢-11-脱氧皮质醇和烟酰胺。总之,GDM后代在老年时表现出明显的糖尿病风险,而n-3 PUFA降低了这种风险。

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