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

Author:

Shahataa Mary Girgis1,Mostafa-Hedeab Gomaa12,Ali Esam Fouaad3,Mahdi Emad ahmed4,Mahmoud Fatma Abd Elhaleem3

Affiliation:

1. Pharmacology Department, Beni Suef University, Beni Suef, Egypt.

2. Pharmacology Department, Faculty of Medicine, Al Jouf University, Al Jouf, Saudia Arabia.

3. Pharmacology Department, Faculty of Medicine, Cairo University, Cairo, Egypt.

4. Pathology Department, Faculty of Veterinary Medicine, Beni Suef University, Egypt.

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.

Publisher

Canadian Science Publishing

Subject

Physiology (medical),Pharmacology,General Medicine,Physiology

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