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过氧化物酶体增殖物激活受体α在调节葡萄糖刺激的胰岛素分泌中的潜在作用。

Potential role of peroxisome proliferator-activated receptor-alpha in the modulation of glucose-stimulated insulin secretion.

作者信息

Sugden Mary C, Holness Mark J

机构信息

Centre for Diabetes and Metabolic Medicine, Institute of Cell and Molecular Science, Barts and the London, Queen Mary's School of Medicine and Dentistry, University of London, London, UK.

出版信息

Diabetes. 2004 Feb;53 Suppl 1:S71-81. doi: 10.2337/diabetes.53.2007.s71.

Abstract

In this review, we discuss the influence of peroxisome proliferator-activated receptor (PPAR)-alpha on islet insulin secretion and develop the hypothesis that modulation of PPAR-alpha function may be important for the regulation of compensatory insulin secretion. We have attempted to analyze the role of PPAR-alpha-linked fatty acid metabolism in islet function in health and in insulin-resistant states linked to lifestyle factors, in particular pregnancy and a diet inappropriately high in saturated fat. We have emphasized the potential for both actions of PPAR-alpha on insulin sensitivity that may be relayed systemically to the islet, leading to modulation of the insulin response in accordance with changes in insulin sensitivity, and direct effects of PPAR-alpha action on the islet itself. Finally, we have developed the concept that compensatory insulin secretion may have a function not only in glucoregulation but also in liporegulation. Thus, augmented insulin secretion may reflect a requirement for lipid lowering as well as for increased glucose disposal and is perceived to aim to compensate for impaired suppression of islet lipid delivery by insulin. This introduces the possibility of a continuum between liporegulation with islet compensation and lipodysregulation leading to islet decompensation in the development of type 2 diabetes.

摘要

在本综述中,我们讨论了过氧化物酶体增殖物激活受体(PPAR)-α对胰岛胰岛素分泌的影响,并提出假说:调节PPAR-α功能可能对代偿性胰岛素分泌的调节具有重要意义。我们试图分析与PPAR-α相关的脂肪酸代谢在健康状态以及与生活方式因素相关的胰岛素抵抗状态(特别是妊娠和饱和脂肪摄入过高的饮食)下胰岛功能中的作用。我们强调了PPAR-α对胰岛素敏感性的两种作用的可能性,一种作用可能通过全身作用传递至胰岛,从而根据胰岛素敏感性的变化调节胰岛素反应,另一种是PPAR-α作用于胰岛本身的直接效应。最后,我们提出了代偿性胰岛素分泌可能不仅在血糖调节中起作用,而且在脂质调节中也起作用的概念。因此,增强的胰岛素分泌可能反映了降低血脂以及增加葡萄糖处置的需求,并且被认为旨在补偿胰岛素对胰岛脂质输送抑制作用的受损。这引入了在2型糖尿病发展过程中,胰岛补偿性脂质调节与导致胰岛失代偿的脂质代谢失调之间存在连续变化的可能性。

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