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利用体内电子顺磁共振波谱法检测自由基代谢产物的形成:苯肼给药后大鼠血红蛋白硫自由基形成的证据。

Detection of free radical metabolite formation using in vivo EPR spectroscopy: evidence of rat hemoglobin thiyl radical formation following administration of phenylhydrazine.

作者信息

Jiang J J, Liu K J, Jordan S J, Swartz H M, Mason R P

机构信息

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

出版信息

Arch Biochem Biophys. 1996 Jun 15;330(2):266-70. doi: 10.1006/abbi.1996.0252.

Abstract

The spin-trapping technique in conjunction with a low-frequency electron paramagnetic (or spin) resonance (EPR or ESR) spectrometer was used to detect the hemoglobin thiyl free radical in living rats using a whole body resonator. The hemoglobin thiyl free radical was formed following the intragastric administration of phenylhydrazine at the LD50 dose of 188 mg/kg. The hemoglobin thiyl free radical was then trapped by preinjected 5,5-dimethyl-1-pyrroline N-oxide (DMPO), which formed the DMPO/hemoglobin thiyl-free radical adduct in the blood. The time course of the in vivo formation and disappearance of the spin adduct was followed. The DMPO/hemoglobin thiyl free radical was detected in blood samples using 9.5 GHz (X-band) and 1.1 GHz (L-band) EPR at room temperature and 77 K. Pretreatment of rats with ascorbate and diethylmaleate (DEM) decreased the signal intensity of the DMPO/hemoglobin thiyl free radical spin adduct. The incubation of ascorbate or DEM at 37 degrees C with rat blood containing preformed DMPO/hemoglobin thiyl radical adduct showed that there was no effect of DEM on the free radical concentration, while ascorbate reduced the radical adduct. This study provided direct evidence of the formation of the DMPO/hemoglobin thiyl free radical in vivo and enabled us to study this formation in living animals free of any artifacts that can occur when using ex vivo methods.

摘要

自旋捕获技术结合低频电子顺磁共振(或自旋)共振(EPR或ESR)光谱仪,使用全身共振器来检测活体大鼠体内的血红蛋白巯基自由基。在以188mg/kg的半数致死剂量经胃内给予苯肼后,形成了血红蛋白巯基自由基。然后,预先注射的5,5-二甲基-1-吡咯啉N-氧化物(DMPO)捕获血红蛋白巯基自由基,该自由基在血液中形成DMPO/血红蛋白巯基自由基加合物。跟踪了自旋加合物在体内形成和消失的时间进程。在室温及77K下,使用9.5GHz(X波段)和1.1GHz(L波段)EPR在血样中检测到DMPO/血红蛋白巯基自由基。用抗坏血酸和马来酸二乙酯(DEM)对大鼠进行预处理可降低DMPO/血红蛋白巯基自由基自旋加合物的信号强度。将抗坏血酸或DEM在37℃下与含有预先形成的DMPO/血红蛋白巯基自由基加合物的大鼠血液一起孵育,结果表明DEM对自由基浓度没有影响,而抗坏血酸可降低自由基加合物。本研究提供了体内形成DMPO/血红蛋白巯基自由基的直接证据,并使我们能够在活体动物中研究这种形成过程,而不会出现使用离体方法时可能产生的任何假象。

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