The Anti-Arthritic Role of Naringenin through Modulating Different T Helper Cells Cytokines, Inflammatory Mediators, Oxidative Stress and Anti-Oxidant Defense System

Osama M. Ahmed, Mohamed Mansour Khalifa, Tarek Atia, Rasha R. Ahmed, Doria A. Abdel-Hafez, Fatema El-Zahraa S., Ahmed A. Damanhory, Mostafa E. Metawee, Abdallah Mohammed Elagali, Sameer Alqassimi, Hader I. Sakr

Article ID: 8164
Vol 38, Issue 7, 2024
DOI: https://doi.org/10.23812/j.biol.regul.homeost.agents.20243807.432
Received: 28 October 2023; Accepted: 28 October 2023; Available online: 20 July 2024; Issue release: 20 July 2024


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Abstract

Background: Rheumatoid arthritis (RA) is a systemic inflammatory disorder that is usually treated with a cocktail of steroidal and nonsteroidal anti-inflammatory drugs, as well as other therapeutic modalities known as disease-modifying anti-rheumatic drugs (DMARDs), all of which have significant side effects. Our objective was to investigate the potential impact of naringenin on a rat model of RA induced by Complete Freunds Adjuvant (CFA). Methods: This was achieved by assessing T-helper (Th) cytokines, oxidative stress, and the anti-oxidant defense system. Eighteen Wistar rats were divided into three equal (n = 6) groups: the normal group, the CFA-induced arthritic control group, and the CFA-induced arthritic group treated with naringenin at a dose of 25 mg/kg body weight daily for two weeks. The study used a variety of techniques, including spectrophotometric analysis, enzyme-linked immunosorbent assay (ELISA), and Western blot procedures, as well as ankle histological investigations and measurement of ankle circumference of the right hind leg. Results: Naringenin treatment significantly decreased the CFA-induced elevated right hind-ankle circumference, serum rheumatoid factor (RF), anti-cyclic citrullinated peptide (ACCP), prostaglandin E2 (PGE2), tumor necrosis factor-α (TNF-α), and serum interleukin (IL)-1β levels (p < 0.05). Naringenin significantly increased serum IL-4 levels, hepatic glutathione (GSH), and superoxide dismutase (SOD) activity when compared to the CFA-induced RA model (p < 0.05). Naringenin treatment decreased ankle joint protein expression of nuclear factor kappa B (NF-κB) p50, NF-κB p65, inhibitor of NF-κB (IκBα), matrix metalloproteinases (MMPs)-1, 3 and 9, and inducible nitric oxide synthase (iNOS), as well as malondialdehyde (MDA) and nitric oxide (NO) levels (p < 0.05). Additionally, there was a significant increase in the ankles nuclear factor erythroid 2-related factor 2 (Nrf2) levels (p < 0.05). Morphological signs like leg swelling and redness were also significantly reduced. Naringenin treatment significantly improved RAs histological changes, such as pannus formation, massive inflammatory cell infiltration, synovial membrane hyperplasia, and articular cartilage erosion. Conclusions: Naringenin has a potent anti-arthritic effect via modulating Th cells cytokines, NF-κB pathway, Nrf2, MMPs, free radical damage, and anti-oxidant defenses.


Keywords

CFA-induced rheumatoid arthritis;naringenin;inflammation;oxidative stress;anti-oxidant defense


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Copyright (c) 2024 Osama M. Ahmed, Mohamed Mansour Khalifa, Tarek Atia, Rasha R. Ahmed, Doria A. Abdel-Hafez, Fatema El-Zahraa S. Abdel Rahman, Ahmed A. Damanhory, Mostafa E. Metawee, Abdallah Mohammed Elagali, Sameer Alqassimi, Hader I. Sakr




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