4.7 Article

Nephroprotective effects of Acacia senegal against aflatoxicosis via targeting inflammatory and apoptotic signaling pathways

Journal

ECOTOXICOLOGY AND ENVIRONMENTAL SAFETY
Volume 262, Issue -, Pages -

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.ecoenv.2023.115194

Keywords

Romania; Mycotoxins; Oxidative stress; Proinflammatory cytokines; Apoptosis; GC; MS; Nutraceuticals

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This study aimed to investigate the protective effects of Acacia gum against AFB1-induced renal damage. The results showed that Acacia gum significantly alleviated the renal dysfunction, oxidative harm, inflammation, and cell death caused by AFB1. These protective effects may be attributed to the antioxidant and anti-inflammatory activities of Acacia gum. The study suggested that Acacia gum supplementation could be used as an add-on agent to food to protect against AFB1-induced nephrotoxicity.
Aflatoxin B1 (AFB1) is a common environmental pollutant that poses a major hazard to both humans and ani-mals. Acacia senegal (Gum) is well-known for having antioxidant and anti-inflammatory bioactive compounds. Our study aimed to scout the nephroprotective effects of Acacia gum (Gum) against AFB1-induced renal damage. Four groups of rats were designed: Control, Gum (7.5 mg/kg), AFB1 (200 & mu;g/kg b.w) and AFB1-Gum, rats were co-treated with both Gum and AFB1. Gas chromatography-mass spectrometry (GC/MS) analysis was done to determine the phytochemical constituents in Gum. AFB1 triggered profound alterations in kidney function pa-rameters (urea, creatinine, uric acid, and alkaline phosphatase) and renal histological architecture. Additionally, AFB1 exposure evoked up-regulation of mRNA expression levels of inflammatory cytokines, including interleukin-6 (IL-6), tumor necrosis factor & alpha; (TNF & alpha;), inducible nitric oxide synthase (iNOS), and nuclear factor kB p65 (NF-& kappa;B/P65) in renal tissue. The oxidative distress and apoptotic cascade are also instigated by AFB1 intoxication as depicted in down-regulated protein expression of the nuclear factor erythroid 2-related factor 2 (Nrf2) and superoxide dismutase type 1 (SOD1) along with upregulation of cytochrome c (Cyto c), and cleaved Caspase3 (Casp3-17 and 19) in renal tissue. In conclusion, current study obviously confirms the alleviating effects of Gum supplementation against AFB1-induced renal dysfunction, oxidative harm, inflammation, and cell death. These mitigating effects are suggested to be attributed to Gum's antioxidant and anti-inflammatory activities. Our results recommend Gum supplementation as add-on agents to food that might aid in protection from AFB1-induced nephrotoxicity.

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