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非甾体抗炎药对人髓过氧化物酶的抑制作用。

Inhibitory effects of non-steroidal anti-inflammatory drugs on human myeloperoxidase.

作者信息

Theron C N, Lubbe S, Van Zyl A

出版信息

S Afr Med J. 1979 Oct 20;56(17):670-5.

PMID:229574
Abstract

Myeloperoxidase with an A420/280 ratio of 0,48 was prepared from normal human leucocytes. This partially purified preparation catalysed guaiacol oxidation, iodination of bovine serum albumin and de-iodination of 125I-thyroxine. Non-steroidal anti-inflammatory drugs (naproxen, indomethacin and flufenamic acid) showed a significant inhibitory effect on myeloperoxidase-catalysed iodination at concentrations of 10(-4)M and higher. Guaiacol also inhibited myeloperoxidase-catalysed iodination, and its iodination inhibition curve was nearly identical to that obtained with the anti-inflammatory drugs. At concentrations between 10(-3)M and 10(-7)M the antiinflammatory drugs had very little or no effect on thyroxine de-iodination. Flufenamic acid and indomethacin, however, inhibited de-iodination significantly at a concentration of 10(-2)M. It is postulated that non-steroidal anti-inflammatory drugs may inhibit myeloperoxidase-catalysed protein iodination by acting as oxidizable cofactors which compete with other oxidizable substrates for oxidants formed by the peroxidase-hydrogen peroxide complex. In view of this and because the myeloperoxidase-hydrogen peroxide system may be involved in inflammatory tissue damage, the possibility should be considered that the action of non-steroidal anti-inflammatory drugs is at least partly attributable to a radical scavenging effect or to sequestration of oxidants.

摘要

从正常人白细胞中制备出A420/280比值为0.48的髓过氧化物酶。这种部分纯化的制剂可催化愈创木酚氧化、牛血清白蛋白碘化以及125I - 甲状腺素的脱碘反应。非甾体抗炎药(萘普生、吲哚美辛和氟芬那酸)在浓度为10^(-4)M及更高时,对髓过氧化物酶催化的碘化反应表现出显著的抑制作用。愈创木酚也抑制髓过氧化物酶催化的碘化反应,其碘化抑制曲线与抗炎药得到的曲线几乎相同。在10^(-3)M至10^(-7)M浓度之间,抗炎药对甲状腺素脱碘反应几乎没有影响或影响极小。然而,氟芬那酸和吲哚美辛在浓度为10^(-2)M时显著抑制脱碘反应。据推测,非甾体抗炎药可能通过作为可氧化的辅因子发挥作用,与其他可氧化底物竞争过氧化物酶 - 过氧化氢复合物形成的氧化剂,从而抑制髓过氧化物酶催化的蛋白质碘化反应。鉴于此,并且由于髓过氧化物酶 - 过氧化氢系统可能参与炎症组织损伤,应考虑非甾体抗炎药的作用至少部分归因于自由基清除效应或氧化剂的螯合作用这一可能性。

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