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Dr. Mona Maher Abd-Elsalam Allam :: Publications:

Title:
Dipeptedyl peptidase-4 (DPP-4) inhibitor downregulates HMGB1/TLR4/NF-ҡB signaling pathway in a diabetic rat model of non-alcoholic fatty liver disease
Authors: Mona M. Allam, Reham M. Ibrahim, Walaa Bayoumie El Gazzar & Mona A. Said
Year: 2021
Keywords: Steatohepatitis; toll-like receptor 4; sitagliptin; highmobility group box 1 protein; nuclear factor-jB
Journal: ARCHIVES OF PHYSIOLOGY AND BIOCHEMISTRY
Volume: Not Available
Issue: Not Available
Pages: Not Available
Publisher: Taylor & Francis Group
Local/International: International
Paper Link: Not Available
Full paper Not Available
Supplementary materials Not Available
Abstract:

Context: Inflammatory and immune pathways play a crucial role in the pathophysiology of non-alcoholic fatty liver disease (NAFLD). Sitagliptin blocks the dipeptidyl peptidase-4 (DPP-4) enzyme, mechanisms that alter inflammatory pathways and the innate immune system, and by which Sitagliptin affects the pathogenesis of NAFLD weren’t previously discussed. Objective: This study aims to understand the interaction between Sitagliptin and innate immune response in order to meliorate NAFLD. Methods: Thirty- two Wistar male albino rats were categorised into four groups. Rats have received a standard diet or a high-fat diet either with or without Sitagliptin. Serum HMGB1, protein and mRNA expressions of hepatic TLR4 and NF-jB, inflammatory cytokines, and histopathological changes were analysed. Results: An ameliorative action of Sitagliptin in NAFLD was demonstrated via decreasing HMGB1- mediated TLR4/NF-jB signalling in order to suppress inflammation and reduce insulin resistance. Conclusion: Sitagliptin may in fact prove to be a beneficial therapeutic intervention in NAFLD.

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