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膳食脂肪酸对胰岛素敏感性和分泌的影响。

Effects of dietary fatty acids on insulin sensitivity and secretion.

作者信息

Manco Melania, Calvani Menotti, Mingrone Geltrude

机构信息

Institute of Internal Medicine, Catholic University, 00168 Rome, Italy.

出版信息

Diabetes Obes Metab. 2004 Nov;6(6):402-13. doi: 10.1111/j.1462-8902.2004.00356.x.

Abstract

Globalization and global market have contributed to increased consumption of high-fat, energy-dense diets, particularly rich in saturated fatty acids( SFAs). Polyunsaturated fatty acids (PUFAs) regulate fuel partitioning within the cells by inducing their own oxidation through the reduction of lipogenic gene expression and the enhancement of the expression of those genes controlling lipid oxidation and thermogenesis. Moreover, PUFAs prevent insulin resistance by increasing membrane fluidity and GLUT4 transport. In contrast, SFAs are stored in non-adipocyte cells as triglycerides (TG) leading to cellular damage as a sequence of their lipotoxicity. Triglyceride accumulation in skeletal muscle cells (IMTG) derives from increased FA uptake coupled with deficient FA oxidation. High levels of circulating FAs enhance the expression of FA translocase the FA transport proteins within the myocites. The biochemical mechanisms responsible for lower fatty acid oxidation involve reduced carnitine palmitoyl transferase (CPT) activity, as a likely consequence of increased intracellular concentrations of malonyl-CoA; reduced glycogen synthase activity; and impairment of insulin signalling and glucose transport. The depletion of IMTG depots is strictly associated with an improvement of insulin sensitivity, via a reduced acetyl-CoA carboxylase (ACC) mRNA expression and an increased GLUT4 expression and pyruvate dehydrogenase (PDH) activity. In pancreatic islets, TG accumulation causes impairment of insulin secretion. In rat models, beta-cell dysfunction is related to increased triacylglycerol content in islets, increased production of nitric oxide, ceramide synthesis and beta-cell apoptosis. The decreased insulin gene promoter activity and binding of the pancreas-duodenum homeobox-1 (PDX-1) transcription factor to the insulin gene seem to mediate TG effect in islets. In humans, acute and prolonged effects of FAs on glucose-stimulated insulin secretion have been widely investigated as well as the effect of high-fat diets on insulin sensitivity and secretion and on the development of type 2 diabetes.

摘要

全球化和全球市场导致了高脂肪、高能量密度饮食的消费增加,尤其是富含饱和脂肪酸(SFA)的饮食。多不饱和脂肪酸(PUFA)通过降低生脂基因表达和增强控制脂质氧化及产热的基因表达来诱导自身氧化,从而调节细胞内的燃料分配。此外,PUFA通过增加膜流动性和葡萄糖转运蛋白4(GLUT4)的转运来预防胰岛素抵抗。相比之下,SFA以甘油三酯(TG)的形式储存在非脂肪细胞中,由于其脂毒性而导致细胞损伤。骨骼肌细胞中甘油三酯的积累(IMTG)源于脂肪酸摄取增加以及脂肪酸氧化不足。高水平的循环脂肪酸会增强脂肪酸转运蛋白(FA translocase)的表达,即肌细胞内的脂肪酸转运蛋白。导致脂肪酸氧化降低的生化机制包括肉碱棕榈酰转移酶(CPT)活性降低,这可能是细胞内丙二酰辅酶A浓度增加的结果;糖原合酶活性降低;以及胰岛素信号传导和葡萄糖转运受损。IMTG储存的消耗与胰岛素敏感性的改善密切相关,这是通过降低乙酰辅酶A羧化酶(ACC)的mRNA表达、增加GLUT4表达和丙酮酸脱氢酶(PDH)活性实现的。在胰岛中,TG积累会导致胰岛素分泌受损。在大鼠模型中,β细胞功能障碍与胰岛中三酰甘油含量增加、一氧化氮生成增加、神经酰胺合成以及β细胞凋亡有关。胰岛素基因启动子活性降低以及胰腺十二指肠同源盒-1(PDX-1)转录因子与胰岛素基因的结合减少似乎介导了TG对胰岛的影响。在人类中,脂肪酸对葡萄糖刺激的胰岛素分泌的急性和长期影响以及高脂饮食对胰岛素敏感性、分泌和2型糖尿病发展的影响也得到了广泛研究。

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