Literature DB >> 20070992

Telmisartan ameliorates hyperglycemia and metabolic profile in nonobese Cohen-Rosenthal diabetic hypertensive rats via peroxisome proliferator activator receptor-gamma activation.

Firas Younis1, Naftali Stern, Rona Limor, Yoram Oron, Sarah Zangen, Talma Rosenthal.   

Abstract

The importance of hypertension treatment has expanded beyond blood pressure management to include additional risk factors, mainly diabetes. It was considered of interest to test the effect of telmisartan, an angiotensin receptor 1 antagonist and peroxisome proliferator activator receptor-gamma partial agonist, on Cohen-Rosenthal diabetic hypertensive nonobese (CRDH) rats, a unique model combining both pathologies. Its effect was examined on fat-derived and inflammatory agents in CRDH. To determine the extent of the drug's peroxisome proliferator activator receptor-gamma modulating beneficial metabolic actions, results were compared with those obtained with valsartan and rosiglitazone in CRDH and Cohen diabetic rat (CDR). Telmisartan and valsartan were given in drinking water at 3 and 12 mg/kg/d, whereas rosiglitazone (3 mg/kg/d) was given as food admixture for a period of 5 months. Blood pressure, glucose, insulin, adiponectin, leptin, and tumor necrosis factor alpha were examined. Telmisartan and valsartan significantly (P < .01) reduced blood pressure, whereas telmisartan and rosiglitazone considerably reduced blood glucose levels to normoglycemic levels (P < .01) in these 2 strains. Insulin levels were not affected by telmisartan and valsartan but were slightly reduced by rosiglitazone in CDR. In contrast to valsartan, adiponectin was significantly (60%, P < .01) increased by telmisartan in both CDR and CRDH, whereas rosiglitazone induced a 60% and 180% increase in CRDH and CDR animals, respectively, on day 30 of treatment. Co-treatment with GW9662 averted telmisartan-induced rise of adiponectin. Tumor necrosis factor alpha declined in telmisartan-treated rats, less so with rosiglitazone, but not valsartan. Telmisartan also induced downsizing of epididymal adipocytes compared with valsartan. Leptin levels were significantly increased by valsartan (P < .05) but reduced by telmisartan and rosiglitazone. The telmisartan-induced increase in adiponectin was most probably associated with a decrease in glucose and tumor necrosis factor alpha levels. Therefore, in addition to its hypotensive effect, telmisartan demonstrated beneficial thiazolidinedione-like effects. Copyright 2010 Elsevier Inc. All rights reserved.

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Year:  2010        PMID: 20070992     DOI: 10.1016/j.metabol.2009.11.013

Source DB:  PubMed          Journal:  Metabolism        ISSN: 0026-0495            Impact factor:   8.694


  8 in total

1.  Rat Models of Metabolic Syndrome.

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2.  Double blockade of angiotensin II (AT(1) )-receptors and ACE does not improve weight gain and glucose homeostasis better than single-drug treatments in obese rats.

Authors:  Anja Miesel; Helge Müller-Fielitz; Olaf Jöhren; Florian M Vogt; Walter Raasch
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3.  PPARs in the Renal Regulation of Systemic Blood Pressure.

Authors:  Tamás Roszer; Mercedes Ricote
Journal:  PPAR Res       Date:  2010-06-08       Impact factor: 4.964

4.  Ang(1-7) treatment attenuates β-cell dysfunction by improving pancreatic microcirculation in a rat model of Type 2 diabetes.

Authors:  L Yuan; Y Li; G Li; Y Song; X Gong
Journal:  J Endocrinol Invest       Date:  2013-04-30       Impact factor: 4.256

5.  Direct renin inhibition modulates insulin resistance in caveolin-1-deficient mice.

Authors:  Somlak Chuengsamarn; Amanda E Garza; Alexander W Krug; Jose R Romero; Gail K Adler; Gordon H Williams; Luminita H Pojoga
Journal:  Metabolism       Date:  2012-09-04       Impact factor: 8.694

6.  Telmisartan and Insulin Resistance in HIV (TAILoR): protocol for a dose-ranging phase II randomised open-labelled trial of telmisartan as a strategy for the reduction of insulin resistance in HIV-positive individuals on combination antiretroviral therapy.

Authors:  Sudeep P Pushpakom; Claire Taylor; Ruwanthi Kolamunnage-Dona; Catherine Spowart; Jiten Vora; Marta García-Fiñana; Graham J Kemp; John Whitehead; Thomas Jaki; Saye Khoo; Paula Williamson; Munir Pirmohamed
Journal:  BMJ Open       Date:  2015-10-15       Impact factor: 2.692

7.  Partial agonist, telmisartan, maintains PPARγ serine 112 phosphorylation, and does not affect osteoblast differentiation and bone mass.

Authors:  Vipula Kolli; Lance A Stechschulte; Abigail R Dowling; Sima Rahman; Piotr J Czernik; Beata Lecka-Czernik
Journal:  PLoS One       Date:  2014-05-08       Impact factor: 3.240

Review 8.  Combating Combination of Hypertension and Diabetes in Different Rat Models.

Authors:  Talma Rosenthal; Firas Younis; Ariela Alter
Journal:  Pharmaceuticals (Basel)       Date:  2010-03-26
  8 in total

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