Elevation of hydrogen peroxide after spinal cord injury detected by using the Fenton reaction

被引:96
作者
Liu, DX
Liu, J
Wen, J
机构
[1] Univ Texas, Med Branch, Dept Neurol, Galveston, TX 77555 USA
[2] Univ Texas, Med Branch, Dept Human Biol Chem & Genet, Galveston, TX 77555 USA
关键词
hydrogen peroxide; reactive oxygen species; iron-catalyzed hydroxyl radical formation; Fenton reaction; secondary damage; spinal cord injury; microdialysis sampling; HPLC analysis; free radicals;
D O I
10.1016/S0891-5849(99)00073-8
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
To reveal whether reactive oxygen species (ROS) play a role after spinal cord injury, we developed a unique method for assaying hydrogen peroxide (H2O2) and determined the time course of its concentration changes following impact injury to the rat spinal cord. Microdialysis was used to sample H2O2 in the extracellular space and the dialysates were collected into a vial containing salicylate and ferrous chloride (FeCl2). H2O2 collected in the vial was converted to hydroxyl radicals (. OH) by FeCl2 catalysis. 2,3- and 2,5-dihydroxybenzoic acid produced by reaction of . OH with salicylate in the collecting vial were measured by HPLC and calibrated to H2O2 concentrations. The postinjury levels of H2O2 were significantly increased (p = 0.02) for over 11 h. FeCl2 administered through the dialysis fiber catalyzes H2O2 conversion in the cord to . OH. This . OH does not reach the collecting vial due to its extremely short lifetime (nanoseconds). The reduced H2O2 levels in the vials validate the measurement of H2O2. The relatively long-lasting formation of H2O2 and superoxide reported herein and previously suggests that ROS may be important in secondary spinal cord damage and that removal, of ROS may be a realistic treatment strategy for reducing injury caused by free radicals. (C) 1999 Elsevier Science Inc.
引用
收藏
页码:478 / 482
页数:5
相关论文
共 34 条
[1]  
Allen A., 1911, J AM MED ASS, V57, P878, DOI 10.1001/jama.1911.04260090100008
[2]  
Anderson D K, 1985, Cent Nerv Syst Trauma, V2, P257
[3]   SPINAL-CORD INJURY AND PROTECTION [J].
ANDERSON, DK ;
DEMEDIUK, P ;
SAUNDERS, RD ;
DUGAN, LL ;
MEANS, ED ;
HORROCKS, LA .
ANNALS OF EMERGENCY MEDICINE, 1985, 14 (08) :816-821
[4]  
BALENTINE JD, 1985, CENTRAL NERVOUS SYST, P455
[5]   APPARENT HYDROXYL RADICAL PRODUCTION BY PEROXYNITRITE - IMPLICATIONS FOR ENDOTHELIAL INJURY FROM NITRIC-OXIDE AND SUPEROXIDE [J].
BECKMAN, JS ;
BECKMAN, TW ;
CHEN, J ;
MARSHALL, PA ;
FREEMAN, BA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (04) :1620-1624
[6]   A RANDOMIZED, CONTROLLED TRIAL OF METHYLPREDNISOLONE OR NALOXONE IN THE TREATMENT OF ACUTE SPINAL-CORD INJURY - RESULTS OF THE 2ND NATIONAL ACUTE SPINAL-CORD INJURY STUDY [J].
BRACKEN, MB ;
SHEPARD, MJ ;
COLLINS, WF ;
HOLFORD, TR ;
YOUNG, W ;
BASKIN, DS ;
EISENBERG, HM ;
FLAMM, E ;
LEOSUMMERS, L ;
MAROON, J ;
MARSHALL, LF ;
PEROT, PL ;
PIEPMEIER, J ;
SONNTAG, VKH ;
WAGNER, FC ;
WILBERGER, JE ;
WINN, HR .
NEW ENGLAND JOURNAL OF MEDICINE, 1990, 322 (20) :1405-1411
[7]   CORRELATION OF METHYLPREDNISOLONE LEVELS IN CAT SPINAL-CORD WITH ITS EFFECTS ON (NA+ + K+)-ATPASE, LIPID-PEROXIDATION, AND ALPHA-MOTOR NEURON FUNCTION [J].
BRAUGHLER, JM ;
HALL, ED .
JOURNAL OF NEUROSURGERY, 1982, 56 (06) :838-844
[8]   EVALUATION OF AN INTENSIVE METHYLPREDNISOLONE SODIUM SUCCINATE DOSING REGIMEN IN EXPERIMENTAL SPINAL-CORD INJURY [J].
BRAUGHLER, JM ;
HALL, ED ;
MEANS, ED ;
WATERS, TR ;
ANDERSON, DK .
JOURNAL OF NEUROSURGERY, 1987, 67 (01) :102-105
[9]   OXYGEN FREE-RADICAL INVOLVEMENT IN ISCHEMIA AND REPERFUSION INJURY TO BRAIN [J].
CAO, W ;
CARNEY, JM ;
DUCHON, A ;
FLOYD, RA ;
CHEVION, M .
NEUROSCIENCE LETTERS, 1988, 88 (02) :233-238
[10]  
CUEVAS P, 1990, ACTA ANAT, V137, P303