Effect of Soy Sauce on Serum Uric Acid Levels in Hyperuricemic Rats and Identification of Flazin as a Potent Xanthine Oxidase Inhibitor

• Published in: Journal of agricultural and food chemistry Vol. 64; no. 23; pp. 4725 - 4734
• Main Authors: Li, Huipin, Zhao, Mouming, Su, Guowan, Lin, Lianzhu, Wang, Yong
• Format: Journal Article
• Language: English
• Published: United States American Chemical Society 15.06.2016
• Subjects: Animals; Body Weight - drug effects; Carbolines - pharmacokinetics; Carbolines - pharmacology; Drug Evaluation, Preclinical - methods; Enzyme Inhibitors - pharmacology; Furans - pharmacokinetics; Furans - pharmacology; Hyperuricemia - chemically induced; Hyperuricemia - diet therapy; Hyperuricemia - drug therapy; Male; Molecular Docking Simulation; Oxonic Acid - adverse effects; Rats, Sprague-Dawley; Soy Foods - analysis; Uric Acid - blood; Xanthine Oxidase - antagonists & inhibitors; Xanthine Oxidase - metabolism; hyperuricemia; soy sauce; flazin; xanthine oxidase inhibitory activity; xanthine oxidase
• ISSN: 0021-8561; 1520-5118
• DOI: 10.1021/acs.jafc.6b01094

This is the first report on the ability of soy sauce to effectively reduce the serum uric acid levels and xanthine oxidase (XOD) activities of hyperuricemic rats. Soy sauce was partitioned sequentially into ethyl acetate and water fractions. The ethyl acetate fraction with strong XOD inhibition effect was purified further. On the basis of xanthine oxidase inhibitory (XOI) activity-guided purification, nine compounds including 3,4-dihydroxy ethyl cinnamate, diisobutyl terephthalate, harman, daidzein, flazin, catechol, thymine, genistein, and uracil were obtained. It was the first time that 3,4-dihydroxy ethyl cinnamate and diisobutyl terephthalate had been identified from soy sauce. Flazin with hydroxymethyl furan ketone group at C-1 and carboxyl at C-3 exhibited the strongest XOI activity (IC50 = 0.51 ± 0.05 mM). According to fluorescence quenching and molecular docking experiments, flazin could enter into the catalytic center of XOD to interact with Lys1045, Gln1194, and Arg912 mainly by hydrophobic forces and hydrogen bonds. Flazin, catechol, and genistein not only were potent XOD inhibitors but also held certain antioxidant activities. According to ADME (absorption, distribution, metabolism, and excretion) simulation in silico, flazin had good oral bioavailability in vivo.