Li Huipin, Zhao Mouming, Su Guowan, Lin Lianzhu, Wang Yong
School of Food Science and Engineering, South China University of Technology , Guangzhou 510640, China.
Guangdong Food Green Processing and Nutrition Regulation Technologies Research Center , Guangzhou 510640, China.
J Agric Food Chem. 2016 Jun 15;64(23):4725-34. doi: 10.1021/acs.jafc.6b01094. Epub 2016 Jun 2.
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.
这是关于酱油有效降低高尿酸血症大鼠血清尿酸水平和黄嘌呤氧化酶(XOD)活性能力的首份报告。酱油依次被分离为乙酸乙酯相和水相。对具有较强XOD抑制作用的乙酸乙酯相进行进一步纯化。在黄嘌呤氧化酶抑制(XOI)活性导向纯化的基础上,获得了9种化合物,包括3,4 - 二羟基乙基肉桂酸酯、对苯二甲酸二异丁酯、哈尔满、大豆苷元、黄酮、儿茶酚、胸腺嘧啶、染料木黄酮和尿嘧啶。3,4 - 二羟基乙基肉桂酸酯和对苯二甲酸二异丁酯首次从酱油中被鉴定出来。在C - 1位带有羟甲基呋喃酮基团且在C - 3位带有羧基的黄酮表现出最强的XOI活性(IC50 = 0.51 ± 0.05 mM)。根据荧光猝灭和分子对接实验,黄酮可进入XOD的催化中心,主要通过疏水作用力和氢键与Lys1045、Gln1194和Arg912相互作用。黄酮、儿茶酚和染料木黄酮不仅是强效的XOD抑制剂,还具有一定的抗氧化活性。根据体内吸收、分布、代谢和排泄(ADME)的计算机模拟,黄酮在体内具有良好的口服生物利用度。