Effect of glutathione augmentation on lipid peroxidation after spinal cord injury

被引:38
作者
Lucas, JH [1 ]
Wheeler, DG [1 ]
Guan, Z [1 ]
Suntres, Z [1 ]
Stokes, BT [1 ]
机构
[1] Ohio State Univ, Dept Physiol & Cell Biol, Coll Med, Columbus, OH 43210 USA
关键词
antioxidants; glutathione; glutathione-S-transferase; 4-HNE; 4-hydroxyalkenals; 4-hydroxy-2-trans-nonenal; malondialdehyde;
D O I
10.1089/08977150260139138
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Lipid peroxidation (LPO) is considered a major factor in damage spread after spinal cord injury (SCI). Therapies that limit LPO after SCI have demonstrated some utility in clinical trials, but more effective treatments are needed. In the present study the effects of augmenting SC levels of the endogenous antioxidant glutathione (GSH) on LPO after SCI were studied in a rat contusion injury model. A significant decrease in GSH occurred 1h after SCI which was paralleled by increases of 123% in malondialdehyde (MDA) and >500% in the 4-hydroxyalkenals (4-HA's), two LPO products. SC irrigation with gamma-glutamyleysteine (GC) preserved GSH and reduced 4-HA's below naive levels but had no effect on MDA. By 24 h after SCI, MDA returned to naive levels but 4-HA's were still elevated. Once again, GC treatment reduced 4-HA's. 4-HA's are much more reactive than MDA and are considered among the most toxic LPO products. These results suggest that (1) conditions after SCI may favor particular branches of the LPO pathway leading to differential LPO product levels, (2) MDA measurement is not by itself an adequate test for the presence or magnitude of LPO after SCI, (3) binding of GSH to 4-HA's may be an important mechanism by which the GSH system confers protection against LPO after SCI, and (4) SC GSH can be augmented after trauma by local irrigation with GC. These results also suggest that GSH augmentation may be an effective strategy for curtailment of LPO-mediated damage in acute phase SCI.
引用
收藏
页码:763 / 775
页数:13
相关论文
共 62 条
[1]   Effect of acrylamide on neurological recovery following spinal cord injury in rats [J].
Al Moutaery, K ;
Morais, C ;
Biary, N ;
Al Deeb, S ;
Tariq, M .
ACTA NEUROCHIRURGICA, 1999, 141 (09) :989-999
[2]  
ANDERSON DK, 1994, NEUROBIOLOGY CENTRAL, P131
[3]   Pretreatment with Alpha Tocopherol Enhances Neurologic Recovery After Experimental Spinal Cord Compression Injury [J].
Anderson, Douglas K. ;
Waters, Thomas R. ;
Means, Eugene D. .
JOURNAL OF NEUROTRAUMA, 1988, 5 (01) :61-67
[4]   GLUTATHIONE MONOETHYL ESTER - PREPARATION, UPTAKE BY TISSUES, AND CONVERSION TO GLUTATHIONE [J].
ANDERSON, ME ;
POWRIE, F ;
PURI, RN ;
MEISTER, A .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1985, 239 (02) :538-548
[5]  
ANUNDI I, 1979, ACTA PHARMACOL TOX, V45, P45
[6]   Impaired mitochondrial function, oxidative stress and altered antioxidant enzyme activities following traumatic spinal cord injury [J].
Azbill, RD ;
Mu, XJ ;
BruceKeller, AJ ;
Mattson, MP ;
Springer, JE .
BRAIN RESEARCH, 1997, 765 (02) :283-290
[7]   The presence of 4-hydroxynonenal/protein complex as an indicator of oxidative stress after experimental spinal cord contusion in a rat model [J].
Baldwin, SA ;
Broderick, R ;
Osbourne, D ;
Waeg, G ;
Blades, DA ;
Scheff, SW .
JOURNAL OF NEUROSURGERY, 1998, 88 (05) :874-883
[8]   LIPID-PEROXIDATION IN EXPERIMENTAL SPINAL-CORD INJURY - TIME-LEVEL RELATIONSHIP [J].
BARUT, S ;
CANBOLAT, A ;
BILGE, T ;
AYDIN, Y ;
COKNESELI, B ;
KAYA, U .
NEUROSURGICAL REVIEW, 1993, 16 (01) :53-59
[9]   A SENSITIVE AND RELIABLE LOCOMOTOR RATING-SCALE FOR OPEN-FIELD TESTING IN RATS [J].
BASSO, DM ;
BEATTIE, MS ;
BRESNAHAN, JC .
JOURNAL OF NEUROTRAUMA, 1995, 12 (01) :1-21
[10]   IDENTIFICATION OF 4-HYDROXYNONEAL AS A CYTO-TOXIC PRODUCT ORIGINATING FROM THE PEROXIDATION OF LIVER MICROSOMAL LIPIDS [J].
BENEDETTI, A ;
COMPORTI, M ;
ESTERBAUER, H .
BIOCHIMICA ET BIOPHYSICA ACTA, 1980, 620 (02) :281-296