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N-3 多不饱和脂肪酸通过延缓肝端粒缩短和调节肝脏代谢来降低妊娠期糖尿病大鼠后代的长期糖尿病风险。

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.

机构信息

Department of Food Science and Nutrition, Zhejiang University, 866 Yuhangtang Road, Hangzhou 310058, China.

Hangzhou Institute for Food and Drug Control, 198 Yonghua Street, Hangzhou 310022, China.

出版信息

Nutrients. 2019 Jul 23;11(7):1699. doi: 10.3390/nu11071699.

Abstract

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.

摘要

妊娠期糖尿病(GDM)对后代的长期影响以及ω-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。健康的后代大鼠在断奶后喂食标准饮食(大豆油)。GDM 后代分为三组:GDM 后代(大豆油)、n-3 PUFA 充足后代(鱼油)和 n-3 PUFA 不足后代(红花油),直至 11 个月大。GDM 后代的糖尿病风险逐渐增加,从断奶时无变化到 11 个月时明显的葡萄糖和胰岛素耐量受损。n-3 PUFA 降低了老年 GDM 后代肝脏中的氧化应激和炎症。n-3 PUFA 和 n-6 PUFA 对 GDM 后代肝脏端粒长度有不同的影响。非靶向代谢组学表明,n-3 PUFA 在肝脏中发挥调节作用,当 GDM 后代长到老年时,许多代谢物和代谢途径发生改变。许多代谢物与糖尿病风险有关,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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b616/6683104/15b2fa57efbd/nutrients-11-01699-g001.jpg

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