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Electrochemical investigation of the inhibition effect of carvacrol on xanthine oxidase activity merging with theoretical studies

机译:碳酸抑制作用对理论研究的X原黄嘌呤氧化酶活性的电化学研究

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One of the key enzymes in purine catabolism is xanthine oxidase (XO), which is widely distributed in human limbs. Due to the excessive activity of XO in the body, hyperuricemia occurs as one of the consequences of uric acid overproduction, which finally leads to gout. In this study, the inhibitory effect of carvacrol on the XO activity was investigated by differential pulse voltammetry (DPV). The results obtained from the experiments strongly overlapped. Therefore, the multivariate curve resolution-alternating least squares (MCR-ALS) method was used to extract valuable information. Analysis of the electrochemical data using MCR-ALS suggested that carvacrol reduces the electrochemical signals of the active centers of XO. The results show that carvacrol can occupy the catalytic centers of enzyme. Also, interaction assays indicated that carvacrol can exert a dose-dependent inhibitory effect on the XO activity. As observed in docking results, carvacrol can penetrate into the active site of XO to interact with some amino acid residues through the formation of hydrogen bonds with Glu 802. In this study, carvacrol proved to have medicinal properties which make it an appropriate dietary adjuvant for prevention and treatment of gout.
机译:嘌呤分解代谢中的一个关键酶是黄嘌呤氧化酶(XO),其广泛分布在人四肢中。由于XO的过度活性在体内,Hiaturocemia作为尿酸过量生产的后果之一,最终导致痛风。在本研究中,通过差分脉冲伏安法(DPV)研究了碳酸对XO活性的抑制作用。从实验中获得的结果强烈重叠。因此,使用多变量曲线分辨率 - 交替的最小二乘(MCR-ALS)方法来提取有价值的信息。使用MCR-ALS的电化学数据分析表明CARVACROL降低了XO活性中心的电化学信号。结果表明,Carvacrol可以占据催化中心。此外,相互作用测定表明,爬行动物可以对XO活性发挥剂量依赖性抑制作用。如在对接结果中所观察到的,Carvacrol可以穿透XO的活性位点,通过形成氢键与Glu 802的氢键相互作用。在本研究中,Carvacrol证明具有药物性质,使其成为适当的膳食佐剂痛风的预防和治疗。

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