Structure-related oxidative damage in rat brain after acute and chronic electroshock

被引:34
作者
Barichello, T
Bonatto, F
Agostinho, FR
Reinke, A
Moreira, JCF
Dal-Pizzol, F
Izquierdo, I
Quevedo, J [1 ]
机构
[1] Univ Extremo Sul Catarinense, Lab Neurotoxicol, BR-88806000 Criciuma, SC, Brazil
[2] Univ Fed Rio Grande Sul, Inst Ciencias Basicas Saude, Dept Bioquim, Ctr Estresse Oxidat, BR-90035003 Porto Alegre, RS, Brazil
[3] Univ Extremo Sul Catarinense, Lab Fisiopatol Expt, BR-88806000 Criciuma, SC, Brazil
[4] Univ Fed Rio Grande Sul, Inst Ciencias Basicas Saude, Dept Bioquim, Ctr Memoria, BR-90035003 Porto Alegre, RS, Brazil
关键词
electroconvulsive shock; electroconvulsive therapy; free radicals; oxidative stress; protein carbonyls; TBARS;
D O I
10.1023/B:NERE.0000035811.06277.b3
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
The role of oxidative stress in electroconvulsive therapy-related effects is not well studied. The purpose of this study was to determine oxidative stress parameters in several brain structures after a single electroconvulsive seizure or multiple electroconvulsive seizures. Rats were given either a single electroconvulsive shock or a series of eight electroconvulsive shocks. Brain regions were isolated, and levels of oxidative stress in the brain tissue ( cortex, hippocampus, striatum and cerebellum) were measured. We demonstrated a decrease in lipid peroxidation and protein carbonyls in the hippocampus, cerebellum, and striatum several times after a single electroconvulsive shock or multiple electroconvulsive shocks. In contrast, lipid peroxidation increases both after a single electroconvulsive shock or multiple electroconvulsive shocks in cortex. In conclusion, we demonstrate an increase in oxidative damage in cortex, in contrast to a reduction of oxidative damage in hippocampus, striatum, and cerebellum.
引用
收藏
页码:1749 / 1753
页数:5
相关论文
共 32 条
[11]   Absence of histological lesions in primate models of ECT and magnetic seizure therapy [J].
Dwork, AJ ;
Arango, V ;
Underwood, M ;
Ilievski, B ;
Rosoklija, G ;
Sackeim, HA ;
Lisanby, SH .
AMERICAN JOURNAL OF PSYCHIATRY, 2004, 161 (03) :576-578
[12]   Electroconvulsive shock in rats: changes in superoxide dismutase and glutathione peroxidase activity [J].
Erakovic, V ;
Zupan, G ;
Varljen, J ;
Radosevic, S ;
Simonic, A .
MOLECULAR BRAIN RESEARCH, 2000, 76 (02) :266-274
[13]   Bilateral near-infrared monitoring of the cerebral concentration and oxygen-saturation of hemoglobin during right unilateral electro-convulsive therapy [J].
Fabbri, F ;
Henry, ME ;
Renshaw, PF ;
Nadgir, S ;
Ehrenberg, BL ;
Franceschini, MA ;
Fantini, S .
BRAIN RESEARCH, 2003, 992 (02) :193-204
[14]  
FINK M, 1989, CONVULSIVE THER, V5, P296
[15]  
Fink M., 1979, Convulsive therapy: theory and practice
[16]   CHRONIC ELECTROCONVULSIVE SHOCK-TREATMENT ELICITS UP-REGULATION OF CRF AND AVP MESSENGER-RNA IN SELECT POPULATIONS OF NEURO-ENDOCRINE NEURONS [J].
HERMAN, JP ;
SCHAFER, MKH ;
SLADEK, CD ;
DAY, R ;
YOUNG, EA ;
AKIL, H ;
WATSON, SJ .
BRAIN RESEARCH, 1989, 501 (02) :235-246
[17]   Mechanism underlying the therapeutic effects of electroconvulsive therapy (ECT) on depression [J].
Ishihara, K ;
Sasa, M .
JAPANESE JOURNAL OF PHARMACOLOGY, 1999, 80 (03) :185-189
[18]  
JANICAK PG, 1985, AM J PSYCHIAT, V142, P297
[19]  
Klamt F, 2001, FREE RADICAL BIO MED, V30, P1137
[20]  
LERER B, 1996, ANN NY ACAD SCI, V462, P366