The redox reaction and biotransformation of rubroskyrin, a modified bis-anthraquione from Penicillium islandicum Sopp.

S Mori, K Kawai, Y Nozawa, Y Ogihara
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引用次数: 3

Abstract

Rubroskyrin, a modified bis-anthraquinone pigment from Penicillium islandicum Sopp, was studied on the redox interaction with NADH-linked redox system of rat liver microsomes, comparing with luteoskyrin and rugulosin. It was found that rubroskyrin was enzymatically reduced by NADH/microsomes and was immediately autoxidized by dissolved oxygen, producing hydrogen peroxide (H2O2). Luteoskyrin and rugulosin did not exhibit such a redox reaction, consuming dissolved oxygen and producing H2O2. The H2O2 production was significantly accelerated by superoxide dismutase (SOD), suggesting the production of superoxide anion during the reduction-autoxidation cycles of rubroskyrin. The thin layer chromatographic (TLC) and spectrophotometric analyses revealed that rubroskyrin was biotransformed by the NADH/microsomes system to stable product(s) which was no longer enzymatically reduced by the NADH/microsome system. From these results it was speculated that the mutagenicity of rubroskyrin might result from the generation of active oxygen by the NADH/microsome-catalyzed redox reaction, and that the redox reaction-linked biotransformation might lead to the elimination of cytotoxicity of rubroskyrin, showing significantly less toxicity than those of luteoskyrin and rugulosin in vivo.
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岛青霉双蒽醌修饰物红霉素的氧化还原反应及生物转化研究。
研究了从岛青霉中提取的一种改性双蒽醌色素红草黄酮与nadh连接的大鼠肝微粒体氧化还原系统的氧化还原相互作用,并与木黄素和红草黄酮进行了比较。结果发现,红霉素被NADH/微粒体酶促还原,并立即被溶解氧氧化,生成过氧化氢(H2O2)。木犀草黄苷和芦黄苷没有发生这样的氧化还原反应,消耗溶解氧并产生H2O2。超氧化物歧化酶(SOD)显著促进了H2O2的生成,提示在红叶草苷还原-自氧化循环过程中产生了超氧阴离子。薄层色谱(TLC)和分光光度分析表明,红霉素被NADH/微粒体系统转化为稳定的产物,不再被NADH/微粒体系统酶还原。由此推测,rubroskrin的致突变性可能是由于NADH/微粒体催化氧化还原反应产生活性氧,氧化还原反应相关的生物转化可能导致rubroskrin的细胞毒性消除,其在体内的毒性明显低于木黄素和rugulosin。
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Erratum: Alfonso D, Johnson HA, Colman-Saizarbitoria T, Presley CP, McCabe GP, McLaughlin JL (1996): SARs of annonaceous acetogenins in rat liver mitochondria. Nat Toxins 4:181-188. Advances in detection methods for fungal and algal toxins. HPLC/MS analysis of fusarium mycotoxins, fumonisins and deoxynivalenol. Neuronal binding of tetanus toxin compared to its ganglioside binding fragment (H(c)). A new type sandwich immunoassay for microcystin: production of monoclonal antibodies specific to the immune complex formed by microcystin and an anti-microcystin monoclonal antibody.
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