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抗坏血酸和谷胱甘肽对六价铬的还原作用,特别涉及大鼠肺脏

Reduction of hexavalent chromium by ascorbic acid and glutathione with special reference to the rat lung.

作者信息

Suzuki Y, Fukuda K

机构信息

Department of Occupational Diseases, National Institute of Industrial Health, Kawasaki, Japan.

出版信息

Arch Toxicol. 1990;64(3):169-76. doi: 10.1007/BF02010721.

Abstract

The reduction of 20 microM hexavalent chromium [chromium(VI)] by L-ascorbic acid (AsA) (0.06-2 mM) and/or glutathione (GSH) (2-15 mM) in buffer solutions, cell-free bronchoalveolar lavage fluids or soluble fractions of rat lungs was investigated at physiological pH (37 degrees C). The reduction in AsA solution was pseudo-first-order in a single phase with respect to chromium(VI), but that in GSH solution showed a two-phase process. The half-life of chromium(IV) ranged from seconds to hours. The reducing ability of AsA was markedly higher than that of GSH. Coexistence of equimolar GSH with AsA accelerated the reduction rate slightly, in comparison with that in the corresponding AsA solution. Lavage fluids containing 0.06 mM AsA showed pH-dependent reactions similar to those of the corresponding AsA solutions. The lung-soluble fractions reduced chromium(VI) in a process composed of phase I and phase II, characterized by the reducing ability of AsA-GSH cooperation and of AsA alone, respectively. Reduction in the former was 30-40% more rapid than in the latter. The biological half-life of chromium(VI) in the lung was estimated to be 0.6 min, on the basis of the reducing activity in the first phase. However, the apparent biological half-life of chromium(VI) was about 2 min in rat lungs after intratracheal injection of chromate, involving depletion of AsA, but no significant changes in GSH. The difference is discussed in terms of AsA-induced initiative reduction in the alveolar lining fluid and subsequent obstructive effects of the resulting trivalent species on trans-membrane permeability of chromate anions.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在生理pH值(37℃)下,研究了L-抗坏血酸(AsA)(0.06 - 2 mM)和/或谷胱甘肽(GSH)(2 - 15 mM)在缓冲溶液、无细胞支气管肺泡灌洗液或大鼠肺可溶性组分中对20 microM六价铬[铬(VI)]的还原作用。AsA溶液中的还原反应在铬(VI)方面为单相准一级反应,但GSH溶液中的反应呈现两相过程。铬(IV)的半衰期从数秒到数小时不等。AsA的还原能力明显高于GSH。与相应的AsA溶液相比,等摩尔GSH与AsA共存时略微加速了还原速率。含有0.06 mM AsA的灌洗液表现出与相应AsA溶液相似的pH依赖性反应。肺可溶性组分在由I相和II相组成的过程中还原铬(VI),其特征分别为AsA - GSH协同作用和AsA单独的还原能力。前者的还原速度比后者快30 - 40%。根据第一阶段的还原活性,估计肺中铬(VI)的生物半衰期为0.6分钟。然而,气管内注射铬酸盐后,大鼠肺中铬(VI)的表观生物半衰期约为2分钟,这涉及AsA的消耗,但GSH无显著变化。从AsA诱导的肺泡衬液中的主动还原以及由此产生的三价物种对铬酸根阴离子跨膜通透性的后续阻碍作用方面对这种差异进行了讨论。(摘要截短至250字)

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