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Review
. 2008;4(2):297-304.
doi: 10.2147/vhrm.s993.

Peroxisome proliferator-activated receptor-gamma agonists and diabetes: current evidence and future perspectives

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Review

Peroxisome proliferator-activated receptor-gamma agonists and diabetes: current evidence and future perspectives

Francesco Chiarelli et al. Vasc Health Risk Manag. 2008.

Abstract

Since their initial availability in 1997, the thiazolidinediones (TZDs) have become one of the most commonly prescribed classes of medications for type 2 diabetes. In addition to glucose control, the TZDs have a number of pleiotropic effects on myriad traditional and non-traditional risk factors for diabetes. TZDs may benefit cardiovascular parameters, such as lipids, blood pressure, inflammatory biomarkers, endothelial function and fibrinolytic state. In this review, we summarise the experimental, preclinical and clinical data regarding the effects of the TZDs in conditions for which they are indicated and discuss their potential in the treatment of other conditions.

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Figures

Figure 1
Figure 1
Molecular mechanisms of Thiazolidinediones. In transactivations, perozisome-proliferator-activated receptor γ (PPARγ) is a nuclear receptor that acts as a transcription factor upon activation. Thiazolidinediones can active PPARγ. On ligand binding, the PPAR forms a heterodimer with the retinoid X receptor (RXR) and they bind to specific peroxisome proliferators response elements (PPRE) on a number of key target genes involved in the carbohydrate and lipid metabolism. In transespression PPARs can repress gene trascription of other pathways, such as nuclear factor −kB (NF-kB).
Figure 2
Figure 2
Clinical effects of Thiazolidinediones.

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