Ellagic Acid Exerts Beneficial Effects on Hyperuricemia by Inhibiting Xanthine Oxidase and NLRP3 Inflammasome Activation

Ellagic Acid
DOI: 10.1021/acs.jafc.1c05239 Publication Date: 2021-10-21T11:51:30Z
ABSTRACT
Hyperuricemia is a metabolic disease caused by impaired uric acid (UA) metabolism. Ellagic (EA) natural small-molecule polyphenolic compound with known antioxidative and anti-inflammatory properties. Here, we evaluated the regulatory effects of EA on hyperuricemia explored underlying mechanisms. We found that an effective xanthine oxidase (XOD) inhibitor (IC50 = 165.6 μmol/L) superoxide anion scavenger 27.66 μmol/L). (5 10 treatment significantly dose-dependently reduced UA levels in L-O2 cells; meanwhile, intraperitoneal administration (50 100 mg/kg) also serum XOD activity hyperuricemic mice markedly improved their liver kidney histopathology. degree foot edema inhibited expression NLPR3 pathway-related proteins tissue monosodium urate (MSU)-treated mice. The effect was observed lipopolysaccharide-stimulated RAW-264.7 cells. Furthermore, expressions NLRP3 (TLR4, p-p65, caspase-1, TNF-α, IL-18) vitro vivo. Our results indicated exerts ameliorative experimental via regulating signaling pathway represents promising therapeutic option for management hyperuricemia.
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