کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
2575061 | 1129737 | 2006 | 9 صفحه PDF | دانلود رایگان |
![عکس صفحه اول مقاله: Molecular activation of PPARγ by angiotensin II type 1-receptor antagonists Molecular activation of PPARγ by angiotensin II type 1-receptor antagonists](/preview/png/2575061.png)
Objective and designElevated blood pressure and insulin resistance are strongly associated in patients. We explored the potential for the anti-hypertensive angiotensin II type 1-receptor (ATR1) antagonists to improve insulin sensitivity through modulation of the nuclear receptor PPARγ, in vitro and in vivo compared to the potent insulin sensitizer, rosiglitazone.MethodsPPARγ modulation by ATR1 antagonists was measured first by direct recruitment of PGC-1, followed by trans-activation reporter assays in cells, and promotion of adipogenesis in fibroblast and pre-adipocyte cell lines. Improvement of insulin sensitivity was measured as changes in levels of glucose, insulin, and adiponectin in ob/ob mice.ResultsTelmisartan, candesartan, irbesartan, and losartan (but not valsartan or olmesartan) each served as bona fide PPARγ ligands in vitro, with EC50 values between 3 and 5 μmol/l. However, only telmisartan, and to a lesser extent candesartan, resulted in significant PPARγ agonism in cells. In vivo, although rosiglitazone significantly lowered both glucose (33%, p < 0.01) and insulin (61%, p < 0.01) levels and increased expression of adiponectin (74%, p < 0.001), sartan treatment had no effect.ConclusionsMany members of the sartan family of ATR1 antagonists are PPARγ ligands in cell-free assays but their modulation of PPARγ in cells is relatively weak. Furthermore, none appear to improve insulin sensitivity in a rodent model under conditions where other insulin sensitizers, including rosiglitazone, do. These results question whether reported effects of sartans on insulin sensitivity may be through other means, and should guide further efforts to develop dual agents to treat hypertension and insulin resistance.
Journal: Vascular Pharmacology - Volume 45, Issue 3, September 2006, Pages 154–162