首页> 外文期刊>Molecular and Cellular Biochemistry: An International Journal for Chemical Biology >Inhibition of xanthine oxidase — xanthine — iron mediated lipid peroxidation by eugenol in liposomes
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Inhibition of xanthine oxidase — xanthine — iron mediated lipid peroxidation by eugenol in liposomes

机译:丁香酚对脂质体中黄嘌呤氧化酶(黄嘌呤)对铁介导的脂质过氧化的抑制作用

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The effect of eugenol on xanthine oxidase (XO) xanthine(X)-Fe+3-ADP mediated lipid peroxidation was studied in liver microsomal lipid liposomes. Eugenol inhibited the lipid peroxidation in a dose dependent manner as assessed by formation of thiobarbituric acid reactive substances. When tested for its effect on XO activity per se, (by measuring uric acid formation) eugenol inhibited the enzyme to an extent of 85% at 10 μm concentration and hence formation of O2 also However, the concentration of eugenol required for XO inhibition was more in presence of metal chelators such as EDTA, EGTA and DETAPAC, but not in presence of deferoxamine, ADP and citrate. The antiperoxidative effect of eugenol was about 35 times more and inhibition of XO was about 5 times higher as compared to the effect of allopurinol. Eugenol did not scavenge O2 generated by phenazine methosulfate and NAD but inhibited propagation of peroxidation catalyzed by Fe2+ EDTA and lipid hydroperoxide containing liposomes. Eugenol inhibits XO-X-Fe+3 ADP mediated peroxidation by inhibiting the XO activity per se in addition to quenching various radical species.
机译:在肝微粒体脂质脂质体中研究了丁香酚对黄嘌呤氧化酶(XO),黄嘌呤(X)-Fe + 3-ADP介导的脂质过氧化的影响。如通过硫代巴比妥酸反应性物质的形成所评估,丁子香酚以剂量依赖性方式抑制脂质过氧化。当测试其本身对XO活性的影响时,丁香酚(通过测量尿酸的形成)在10μm浓度下将酶抑制到85%的程度,因此也形成了O2。但是,抑制XO所需的丁香酚的浓度更高在金属螯合剂(例如EDTA,EGTA和DETAPAC)中,但在去铁胺,ADP和柠檬酸盐中则不存在。与别嘌醇相比,丁子香酚的抗过氧化作用高约35倍,对XO的抑制作用约高5倍。丁香酚不能清除由吩嗪硫酸甲酯和NAD产生的O2,但可以抑制由Fe2 + EDTA和脂质过氧化脂质体催化的过氧化反应的传播。丁子香酚除淬灭各种自由基外,还通过抑制XO本身的活性来抑制XO-X-Fe + 3 ADP介导的过氧化。

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