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血红素加氧酶的金属诱导作用。

Metal induction of heme oxygenase.

作者信息

Sunderman F W

机构信息

Department of Laboratory Medicine, University of Connecticut School of Medicine, Farmington 06032.

出版信息

Ann N Y Acad Sci. 1987;514:65-80. doi: 10.1111/j.1749-6632.1987.tb48762.x.

Abstract

The experimental data that have been reviewed support the following conclusions regarding metal induction of microsomal heme oxygenase activity: 1. Induction of heme oxygenase in liver, kidney, and other organs of rodents is a nonspecific, toxic response to parenteral administration of numerous metal compounds. 2. The Co2+ and Cd2+ ions are especially potent for induction of heme oxygenase in rat liver; Sn2+, Ni2+, and As3+ are especially potent for induction of the enzyme in rat kidney; Hg2+ is especially potent for induction of the enzyme in rat adrenal. 3. Rat spleen, testis, and brain are relatively refractory to metal induction of heme oxygenase activity; in testicular microsomes from Cd2+-treated rats, heme oxygenase activity is markedly inhibited. 4. Metal induction of heme oxygenase requires de novo synthesis of mRNA and protein, based on 1) experiments with metabolic inhibitors (actinomycin D, puromycin, and cycloheximide) and 2) translation assays of heme oxygenase mRNA. 5. Heme oxygenase induction by metals is generally suppressed by treatments with SH compounds (for example, cysteine and glutathione) and enhanced by agents that deplete tissue SH levels (for example, diethyl maleate), suggesting that the induction mechanism may involve binding of metal ions to SH-containing regulatory molecules. 6. Administration of DDC exerts a pronounced synergistic effect on Ni2+ induction of heme oxygenase activity in rat tissues, attributable in part to enhanced cellular uptake of nickel. 7. Induction of heme oxygenase is not sustained during repeated daily treatments of rats with NiCl2, pointing to an adaptive mechanism for tolerance to the enzyme inducer. Investigations of metal induction of heme oxygenase activity have commonly involved sc or ip administration of the test compounds to rats. The paucity of studies in other species and the dearth of experiments with oral or respiratory exposures hinder extrapolations of the animal data to human environmental or occupational exposures to metal compounds.

摘要

已审阅的实验数据支持以下关于金属诱导微粒体血红素加氧酶活性的结论

  1. 啮齿动物肝脏、肾脏及其他器官中血红素加氧酶的诱导是对多种金属化合物肠胃外给药的一种非特异性毒性反应。2. Co2+和Cd2+离子对诱导大鼠肝脏中的血红素加氧酶特别有效;Sn2+、Ni2+和As3+对诱导大鼠肾脏中的该酶特别有效;Hg2+对诱导大鼠肾上腺中的该酶特别有效。3. 大鼠脾脏、睾丸和大脑对金属诱导血红素加氧酶活性相对不敏感;在经Cd2+处理的大鼠的睾丸微粒体中,血红素加氧酶活性受到明显抑制。4. 基于1)用代谢抑制剂(放线菌素D、嘌呤霉素和环己酰亚胺)进行的实验以及2)血红素加氧酶mRNA的翻译分析,金属诱导血红素加氧酶需要mRNA和蛋白质的从头合成。5. 金属对血红素加氧酶的诱导通常会被SH化合物(例如半胱氨酸和谷胱甘肽)处理所抑制,并被消耗组织SH水平的试剂(例如马来酸二乙酯)增强,这表明诱导机制可能涉及金属离子与含SH的调节分子的结合。6. 给予二乙基二硫代氨基甲酸钠(DDC)对大鼠组织中Ni2+诱导血红素加氧酶活性有明显的协同作用,部分原因是细胞对镍的摄取增加。7. 用NiCl2对大鼠进行每日重复处理期间,血红素加氧酶的诱导不会持续,这表明存在对酶诱导剂的耐受适应机制。对血红素加氧酶活性的金属诱导的研究通常涉及对大鼠皮下或腹腔注射受试化合物。其他物种的研究较少,且缺乏口服或呼吸道暴露的实验,这阻碍了将动物数据外推至人类对金属化合物的环境或职业暴露情况。

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