Literature DB >> 27245695

Effects of telmisartan and pioglitazone on high fructose induced metabolic syndrome in rats.

Mary Girgis Shahataa1, Gomaa Mostafa-Hedeab1,2, Esam Fouaad Ali3, Emad Ahmed Mahdi4, Fatma Abd Elhaleem Mahmoud3.   

Abstract

Metabolic syndrome (MS) is a cluster of hypertension, insulin resistance, dyslipidaemia, and hyperuricemia. This study was designed to assess the effect of telmisartan and pioglitazone on high fructose induced MS. Thirty-five male albino rats were classified into 5 groups: A, normal diet; B, high-fructose diet (HFD) subdivided into B1 (HFD only), B2 (telmisartan, 5 mg/kg), B3 (pioglitazone, 10 mg/kg), and B4 (telmisartan + pioglitazone). Administration of the drugs was started after the rats had been on HFD for 4 weeks and continued for 4 weeks. Body mass (BM), blood pressure (BP), uric acid (UA), total cholesterol, triglycerides (TG), high-density lipoprotein (HDL-c), low-density lipoprotein (LDL-c), blood urea nitrogen (BUN), creatinine, and nitric oxide (NO) were measured and the levels of fasting glucose and fasting insulin were estimated. Compared with group B1, telmisartan treatment significantly decreased BP, BM, serum glucose, insulin, UA, urea, cholesterol, TGA, and LDL and significantly increased HDL, whereas pioglitazone treatment significantly decreased BP, serum glucose, insulin, UA, urea, creatinine, cholesterol, TGA, and LDL and significantly increased HDL. Co-administration of pioglitazone + telmisartan significantly decreased insulin, urea, and creatinine compared with telmisartan alone. Combined telmisartan + pioglitazone allowed better control of BP, hyperglycaemia, insulin resistance, and the amelioration of BM increase that may be associated with pioglitazone treatment.

Entities:  

Keywords:  acide urique; blood pressure; body mass; dyslipidaemia; dyslipidémie; insulin resistance; metabolic syndrome; pioglitazone; poids corporel; résistance à l’insuline; syndrome métabolique; telmisartan; tension artérielle; uric acid

Mesh:

Substances:

Year:  2016        PMID: 27245695     DOI: 10.1139/cjpp-2016-0090

Source DB:  PubMed          Journal:  Can J Physiol Pharmacol        ISSN: 0008-4212            Impact factor:   2.273


  8 in total

1.  Development and validation of a high throughput LC-MS/MS method for simultaneous quantitation of pioglitazone and telmisartan in rat plasma and its application to a pharmacokinetic study.

Authors:  Pinaki Sengupta; Bappaditya Chatterjee; Uttam Kumar Mandal; Bapi Gorain; Tapan Kumar Pal
Journal:  J Pharm Anal       Date:  2017-05-19

2.  Regulatory landscape of AGE-RAGE-oxidative stress axis and its modulation by PPARγ activation in high fructose diet-induced metabolic syndrome.

Authors:  Luca Cannizzaro; Giuseppe Rossoni; Federica Savi; Alessandra Altomare; Cristina Marinello; Thammakorn Saethang; Marina Carini; D Michael Payne; Trairak Pisitkun; Giancarlo Aldini; Asada Leelahavanichkul
Journal:  Nutr Metab (Lond)       Date:  2017-01-13       Impact factor: 4.169

Review 3.  What is the role of angiotensin receptor blockers in treatment of hyperuricemia coexisting with arterial hypertension?

Authors:  Barbara Nieradko-Iwanicka
Journal:  Reumatologia       Date:  2018-05-09

4.  Pioglitazone and PPAR-γ modulating treatment in hypertensive and type 2 diabetic patients after ischemic stroke: a national cohort study.

Authors:  Chi-Hung Liu; Tsong-Hai Lee; Yu-Sheng Lin; Pi-Shan Sung; Yi-Chia Wei; Yan-Rong Li
Journal:  Cardiovasc Diabetol       Date:  2020-01-07       Impact factor: 9.951

5.  Impact of a long-term high-fructose diet on systemic metabolic profiles of mice.

Authors:  Changmeng Cui; Changshui Wang; Shasha Han; Dingyi Yu; Li Zhu; Pei Jiang
Journal:  FASEB Bioadv       Date:  2022-05-16

6.  Epigallocatechin gallate ameliorates tetrahydrochloride-induced liver toxicity in rats via inhibition of TGFβ / p-ERK/p-Smad1/2 signaling, antioxidant, anti-inflammatory activity.

Authors:  Gomaa Mostafa-Hedeab; Manal Ewaiss Hassan; Taher F Halawa; Farooq Ahmed Wani
Journal:  Saudi Pharm J       Date:  2022-06-27       Impact factor: 4.562

7.  Dietary Fructose Increases the Sensitivity of Proximal Tubules to Angiotensin II in Rats Fed High-Salt Diets.

Authors:  Agustin Gonzalez-Vicente; Nancy J Hong; Nianxin Yang; Pablo D Cabral; Jessica M Berthiaume; Fernando P Dominici; Jeffrey L Garvin
Journal:  Nutrients       Date:  2018-09-06       Impact factor: 5.717

8.  Paeoniflorin Ameliorates Fructose-Induced Insulin Resistance and Hepatic Steatosis by Activating LKB1/AMPK and AKT Pathways.

Authors:  Yu-Cheng Li; Jing-Yi Qiao; Bao-Ying Wang; Ming Bai; Ji-Duo Shen; Yong-Xian Cheng
Journal:  Nutrients       Date:  2018-08-05       Impact factor: 5.717

  8 in total

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