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苯肼给药后大鼠体内血红蛋白巯基自由基的形成。

In vivo rat hemoglobin thiyl free radical formation following phenylhydrazine administration.

作者信息

Maples K R, Jordan S J, Mason R P

机构信息

Laboratory of Molecular Biophysics, National Institute of Environmental Health Sciences, Research Triangle Park, North Carolina 27709.

出版信息

Mol Pharmacol. 1988 Mar;33(3):344-50.

PMID:2832722
Abstract

The reaction of oxyhemoglobin with phenylhydrazine has received considerable attention for many decades. The basis for this interest stems from the ability of phenylhydrazine and hydrazine-based drugs to induce hemolytic anemia. Considerable evidence obtained from in vitro ESR experiments implicates free radicals in the events leading to red blood cell hemolysis. However, until this report, no corroborating ESR evidence for in vivo free radical formation has been presented. We have successfully employed ESR to detect the formation of a radical adduct in the blood of rats which received an intragastric dose of phenylhydrazine followed by an intraperitoneal injection of the spin trap 5,5-dimethyl-1-pyrroline N-oxide (DMPO). An immobilized radical adduct was detected by ESR when phenylhydrazine was administered in a dosage comparable to that prescribed for currently employed hydrazine-based drugs. We were also able to detect this immobilized DMPO adduct when hydrazine was employed in place of phenylhydrazine in the rat studies. The results of a series of experiments led us to ascribe this DMPO radical adduct to the trapping of a hemoglobin-derived thiyl free radical.

摘要

几十年来,氧合血红蛋白与苯肼的反应一直备受关注。这种关注的依据源于苯肼和基于肼的药物诱发溶血性贫血的能力。从体外电子自旋共振(ESR)实验获得的大量证据表明,自由基参与了导致红细胞溶血的过程。然而,在本报告之前,尚未有体内自由基形成的确证ESR证据。我们成功地利用ESR检测到,在给大鼠灌胃苯肼后腹腔注射自旋捕获剂5,5 - 二甲基 - 1 - 吡咯啉N - 氧化物(DMPO)的情况下,大鼠血液中形成了一种自由基加合物。当以与目前使用的基于肼的药物规定剂量相当的剂量给予苯肼时,通过ESR检测到了一种固定化的自由基加合物。在大鼠研究中,当用肼代替苯肼时,我们也能够检测到这种固定化的DMPO加合物。一系列实验的结果使我们将这种DMPO自由基加合物归因于血红蛋白衍生的硫自由基的捕获。

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