Effects of Sitagliptin Treatment on Dysmetabolism, Inflammation, and Oxidative Stress in an Animal Model of Type 2 Diabetes (ZDF Rat)

Author:

Ferreira Liliana1,Teixeira-de-Lemos Edite12,Pinto Filipa1,Parada Belmiro1,Mega Cristina2,Vala Helena2,Pinto Rui3,Garrido Patrícia1,Sereno José1,Fernandes Rosa1,Santos Paulo4,Velada Isabel4,Melo Andreia1,Nunes Sara1,Teixeira Frederico15,Reis Flávio15

Affiliation:

1. Institute of Pharmacology & Experimental Therapeutics, IBILI, Medicine Faculty, University of Coimbra, 3000-354 Coimbra, Portugal

2. ESAV, Polytechnic Institute of Viseu, 3500 Viseu, Portugal

3. Pharmacology & Pharmacotoxicology Unit, Faculty of Pharmacy, Lisbon University, 1649-003 Lisboa, Portugal

4. Functional Genomics Laboratory, Center of Histocompatibility of the Centre, 3001-301 Coimbra, Portugal

5. Institute for Molecular and Cellular Biology, Porto University, 4150 Porto, Portugal

Abstract

The purpose of this paper is to evaluate the chronic effect of sitagliptin on metabolic profile, inflammation, and redox status in the Zucker Diabetic Fatty (ZDF) rat, an animal model of obese type 2 diabetes. Diabetic and obese ZDF (fa/fa) rats and their controls (ZDF +/+) were treated during 6 weeks with vehicle (control) and sitagliptin (10 mg/kg/bw). Glucose, HbA1c, insulin, Total-c, TGs, IL-1β, TNF-α, CRPhs, and adiponectin were assessed in serum and MDA and TAS in serum, pancreas, and heart. Pancreatic histology was also evaluated. Sitagliptin in diabetic rats promoted a decrease in glucose, HbA1c, Total-c, and TGs accompanied by a partial prevention of insulinopenia, together, with a decrease in CRPhsand IL-1β. Sitagliptin also showed a positive impact on lipid peroxidation and hypertension prevention. In conclusion, chronic sitagliptin treatment corrected the glycaemic dysmetabolism, hypertriglyceridaemia, inflammation, and hypertension, reduced the severity of the histopathological lesions of pancreatic endocrine and exocrine tissues, together with a favourable redox status, which might be a further advantage in the management of diabetes and its proatherogenic comorbidities.

Funder

Merck Sharp & Dohme Foundation

Publisher

Hindawi Limited

Subject

Cell Biology,Immunology

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