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叔丁基过氧化氢对兔血小板中花生四烯酸环氧化酶和脂氧合酶代谢的影响。

Effect of tert-butyl hydroperoxide on cyclooxygenase and lipoxygenase metabolism of arachidonic acid in rabbit platelets.

作者信息

Fujimoto Y, Takai S, Matsuno K, Sumiya T, Nishida H, Sakuma S, Fujita T

机构信息

Department of Hygienic Chemistry, Osaka University of Pharmaceutical Sciences, Japan.

出版信息

Prostaglandins Leukot Essent Fatty Acids. 1992 Dec;47(4):259-64. doi: 10.1016/0952-3278(92)90195-o.

Abstract

The effect of tert-butyl hydroperoxide (t-BOOH) on the formation of thromboxane (TX) B2, 12-hydroxy-5,8,10-heptadecatrienoic acid (HHT) and 12-hydroxy-5,8,10,14-eicosatetraenoic acid (12-HETE) from exogenous arachidonic acid (AA) in washed rabbit platelets was examined. t-BOOH enhanced TXB2 and HHT formation at concentrations of 8 microM and below, and at 50 microM it inhibited the formation, suggesting that platelet cyclooxygenase activity can be enhanced or inhibited by t-BOOH depending on the concentration. t-BOOH inhibited 12-HETE production in a dose-dependent manner. When the platelets were incubated with 12-hydroperoxy-5,8,10,14-eicosatetraenoic acid (12-HPETE) instead of AA, t-BOOH failed to inhibit the conversion of 12-HPETE to 12-HETE, indicating that the inhibition of 12-HETE formation by t-BOOH occurs at the lipoxygenase step. Studies utilizing indomethacin (a selective cyclooxygenase inhibitor) and desferrioxamine (an iron-chelating agent) revealed that the inhibitory effect of t-BOOH on the lipoxygenase is not mediated through the activation of the cyclooxygenase and that this effect of t-BOOH is due to the hydroperoxy moiety. These results suggest that hydroperoxides play an important role in the control of platelet cyclooxygenase and lipoxygenase activities.

摘要

研究了叔丁基过氧化氢(t-BOOH)对洗涤过的兔血小板中,外源性花生四烯酸(AA)生成血栓素(TX)B2、12-羟基-5,8,10-十七碳三烯酸(HHT)和12-羟基-5,8,10,14-二十碳四烯酸(12-HETE)的影响。在浓度为8 microM及以下时,t-BOOH增强TXB2和HHT的生成,而在50 microM时则抑制其生成,这表明t-BOOH可根据浓度增强或抑制血小板环氧化酶活性。t-BOOH以剂量依赖性方式抑制12-HETE的产生。当血小板与12-氢过氧-5,8,10,14-二十碳四烯酸(12-HPETE)而非AA一起孵育时,t-BOOH未能抑制12-HPETE向12-HETE的转化,这表明t-BOOH对12-HETE生成的抑制作用发生在脂氧合酶步骤。使用吲哚美辛(一种选择性环氧化酶抑制剂)和去铁胺(一种铁螯合剂)的研究表明,t-BOOH对脂氧合酶的抑制作用不是通过环氧化酶的激活介导的,且t-BOOH的这种作用归因于氢过氧基部分。这些结果表明,氢过氧化物在控制血小板环氧化酶和脂氧合酶活性中起重要作用。

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