Suppr超能文献

过氧化物酶体增殖物激活受体(PPARs)配体的临床意义。

Clinical interest of PPARs ligands.

作者信息

Vergès B

机构信息

Service d'Endocrinologie, Diabétologie et Maladies Métaboliques, hôpital du Bocage, CHU de Dijon, France.

出版信息

Diabetes Metab. 2004 Feb;30(1):7-12. doi: 10.1016/s1262-3636(07)70083-6.

Abstract

Cardiovascular disease is significantly increased in patients with metabolic syndrome and type 2 diabetes. Several factors such as chronic hyperglycemia, lipId abnormalities, endothelium dysfunction, inflammation, oxIdative stress, increased thrombosis and decreased fibrinolysis are likely to promote cardiovascular events in these patients. Because of positive effects on glucose homeostasis, lipId metabolism, proteins involved in all stages of atherogenesis, endothelium function, inflammation, thrombosis and fibrinolysis, PPARS alpha (fibrates) and PPARs gamma (glitazones) agonists are good candIdates to reduce cardiovascular disease, more precisely in subjects with metabolic syndrome or type 2 diabetes. PPARS alpha agonists (fibrates) are potent hypolipIdemic agents increasing plasma HDL-cholesterol and reducing free fatty acIds, triglycerIdes, LDL-cholesterol and the number of small dense LDL pArticles. Moreover, they reduce vascular inflammation and thrombosis, promote fibrinolysis and inhibit the production of the vasoconstrictor factor, endothelin-1, by the endothelium. They have been shown, in clinical trials, to reduce cardiovascular disease, more particularly in patients displaying lipId abnormalities typical of metabolic syndrome and type 2 diabetes (high triglycerIdes, low HDL-cholesterol). PPARS gamma agonists (glitazones) have not only beneficial effects on glucose homeostasis, by increasing insulin sensitivity and reducing blood glucose level but also on lipId metabolism by elevating plasma HDL-cholesterol, decreasing free fatty acIds and the number of small dense LDL pArticles, and for pioglitazone by reducing plasma triglycerIdes. Furthermore, they diminish vascular inflammation and vasoconstriction, inhibit monocyte chemotaxis, proliferation and migration of smooth muscle cells, in the vascular wall and decrease the production of adhesion molecules and metalloproteinases. PPARs gamma agonists (glitazones) have been shown to reduce the development of atherosclerotic lesions in rats. The potential clinical benefit of PPARs gamma agonists on the reduction of cardiovascular disease, in type 2 diabetic patients, will be specified by the ongoing intervention studies.

摘要

代谢综合征和2型糖尿病患者的心血管疾病显著增加。慢性高血糖、脂质异常、内皮功能障碍、炎症、氧化应激、血栓形成增加和纤维蛋白溶解减少等多种因素可能促使这些患者发生心血管事件。由于对葡萄糖稳态、脂质代谢、动脉粥样硬化发生各阶段涉及的蛋白质、内皮功能、炎症、血栓形成和纤维蛋白溶解具有积极作用,过氧化物酶体增殖物激活受体α(贝特类药物)和过氧化物酶体增殖物激活受体γ(格列酮类药物)激动剂是降低心血管疾病的良好候选药物,更确切地说是在代谢综合征或2型糖尿病患者中。过氧化物酶体增殖物激活受体α激动剂(贝特类药物)是强效降血脂药物,可提高血浆高密度脂蛋白胆固醇水平,降低游离脂肪酸、甘油三酯、低密度脂蛋白胆固醇水平以及小而密低密度脂蛋白颗粒的数量。此外,它们可减轻血管炎症和血栓形成,促进纤维蛋白溶解,并抑制内皮细胞产生血管收缩因子内皮素-1。在临床试验中已表明,它们可降低心血管疾病风险,尤其是在表现出代谢综合征和2型糖尿病典型脂质异常(高甘油三酯、低高密度脂蛋白胆固醇)的患者中。过氧化物酶体增殖物激活受体γ激动剂(格列酮类药物)不仅通过提高胰岛素敏感性和降低血糖水平对葡萄糖稳态有有益作用,还通过提高血浆高密度脂蛋白胆固醇水平、降低游离脂肪酸和小而密低密度脂蛋白颗粒数量以及(对于吡格列酮而言)降低血浆甘油三酯水平对脂质代谢有有益作用。此外,它们可减轻血管炎症和血管收缩,抑制单核细胞趋化作用、血管壁平滑肌细胞的增殖和迁移,并减少黏附分子和金属蛋白酶的产生。过氧化物酶体增殖物激活受体γ激动剂(格列酮类药物)已被证明可减少大鼠动脉粥样硬化病变的发展。正在进行的干预研究将明确过氧化物酶体增殖物激活受体γ激动剂对2型糖尿病患者降低心血管疾病的潜在临床益处。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验