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噻唑烷二酮类药物对血清脂蛋白水平的影响。

Impact of thiazolidenediones on serum lipoprotein levels.

作者信息

Goldberg Ronald B

机构信息

Division of Endocrinology, Diabetes and Metabolism, University of Miami Miller School of Medicine, 1450 NW 10th Avenue, Miami, FL 33136, USA.

出版信息

Curr Atheroscler Rep. 2006 Sep;8(5):397-404. doi: 10.1007/s11883-006-0037-5.

Abstract

The thiazolidinediones, acting through peroxisome proliferator-activated receptor chi (PPARchi), affect multiple areas of metabolism. Of increasing importance is the recognition that these agents affect lipoprotein metabolism and cause changes in serum lipid and lipoprotein levels. All three thiazolidinediones, including troglitazone (which was withdrawn in the year 2000), rosiglitazone, and pioglitazone, tend to increase high-density lipoprotein (HDL) cholesterol, increase the size/decrease the density of low-density lipoprotein (LDL) particles, and raise the level of lipoprotein(a). In addition, troglitazone and pioglitazone, but not rosiglitazone, lower triglyceride levels modestly, thereby further contributing to increases in LDL and HDL size. The mechanism for these effects is still being clarified, but may involve enhancement of triglyceride clearance (in the case of pioglitazone), alteration of apolipoprotein C-III levels, reduction of hepatic lipase, and increase in ATP binding cassette A1 (ABCA1) activity. The clinical implications of these effects need further exploration.

摘要

噻唑烷二酮类药物通过过氧化物酶体增殖物激活受体γ(PPARγ)发挥作用,影响多个代谢领域。越来越重要的是认识到这些药物会影响脂蛋白代谢,并导致血清脂质和脂蛋白水平发生变化。所有三种噻唑烷二酮类药物,包括曲格列酮(已于2000年撤市)、罗格列酮和吡格列酮,都倾向于升高高密度脂蛋白(HDL)胆固醇,增加低密度脂蛋白(LDL)颗粒的大小/降低其密度,并提高脂蛋白(a)的水平。此外,曲格列酮和吡格列酮,但不包括罗格列酮,可适度降低甘油三酯水平,从而进一步促使LDL和HDL大小增加。这些作用的机制仍在阐明中,但可能涉及甘油三酯清除增强(就吡格列酮而言)、载脂蛋白C-III水平改变、肝脂肪酶减少以及ATP结合盒转运体A1(ABCA1)活性增加。这些作用的临床意义需要进一步探索。

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