Neuroprotective actions of vitamin C related to decreased lipid peroxidation and increased catalase activity in adult rats after pilocarpine-induced seizures

被引:76
作者
Santos, Lucia F. L. [1 ]
Freitas, Rizangela L. M. [1 ]
Xavier, Sarah M. L. [1 ]
Saldanha, Glaucio B. [1 ]
Freitas, Rivelilson M. [1 ]
机构
[1] Curso Farm Fac Catolica Rainha Sertao, BR-6390000 Quixada, Brazil
关键词
vitamin C; pilocarpine; hippocampus; lipid peroxidation; catalase; seizures;
D O I
10.1016/j.pbb.2007.10.007
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
In the present study, we examined the neuroprotective effects of vitarnin C in adult rats after pilocarpine-induced seizures. Vitamin C is an exogenous antioxidant that. can be used in treatment of seizures. It can alter oxidative stress and damage neuronal induced by seizures. Its antioxidant properties can be proved in epilepsy models, such as pilocarpine-induced seizures in adult rats. In order to investigate neuroprotective effects of vitamin C, adult male rats (2 months-old) were pretreated with vitamin C (VIT C 250 mg/kg, i.p.) 30 min before receiving pilocarpine (400 mg/kg, s.c., P400 group). The other three groups were treated with vitamin C (VIT C group) and saline 0.9 (control group) alone. The pretreatment with vitamin C increased the latency to first seizures and reduced mortality rate after pilocarpine-induced seizures. Pretreatment with vitamin C alone decrease lipid peroxidation levels when compared to pilocarpine group and P400+VIT C. In P400, P400+VIT C and VIT C groups were observed an increased hippocampal catalase activity when compared to control group. Our results can suggest that neuroprotective effects of vitamin C in adult rats can be the result of reduced lipid peroxidation levels and increase of catalase activity after seizures and status epilepticus induced by pilocarpine. (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:1 / 5
页数:5
相关论文
共 16 条
[1]   Superoxide dismutase, glutathione peroxidase activities and the hydroperoxide concentration are modified in the hippocampus of epileptic rats [J].
Bellissimo, MI ;
Amado, D ;
Abdalla, DSP ;
Ferreira, EC ;
Cavalheiro, EA ;
Naffah-Mazzacoratti, MD .
EPILEPSY RESEARCH, 2001, 46 (02) :121-128
[2]   THE PILOCARPINE MODEL OF EPILEPSY [J].
CAVALHEIRO, EA .
ITALIAN JOURNAL OF NEUROLOGICAL SCIENCES, 1995, 16 (1-2) :33-37
[3]   ASSAY OF CATALASES AND PEROXIDASES [J].
CHANCE, B ;
MAEHLY, AC .
METHODS IN ENZYMOLOGY, 1955, 2 :764-775
[4]  
Costa L G:., 1994, Principles of neurotoxicology, P475
[5]   Lipid peroxidation in hippocampus early and late after status epilepticus induced by pilocarpine or kainic acid in Wistar rats [J].
Dal-Pizzol, F ;
Klamt, F ;
Vianna, MMR ;
Schröder, N ;
Quevedo, J ;
Benfato, MS ;
Moreira, JCF ;
Walz, R .
NEUROSCIENCE LETTERS, 2000, 291 (03) :179-182
[6]   The influence of calcium channel blockers on the brain free fatty acid level and glutathione peroxidase activity in rats with lithium and pilocarpine-induced status epilepticus [J].
Erakovic, V ;
Zupan, G ;
Varljen, J ;
Simonic, A .
NEUROSCIENCE RESEARCH COMMUNICATIONS, 2002, 30 (02) :111-119
[7]  
Ferreira A L, 1997, Rev Assoc Med Bras (1992), V43, P61
[8]   Pilocarpine-induced status epilepticus in rats: lipid peroxidation level, nitrite formation, GABAergic and glutamatergic receptor alterations in the hippocampus, striatum and frontal cortex [J].
Freitas, RM ;
Sousa, FCF ;
Vasconcelos, SMM ;
Viana, GSB ;
Fonteles, MMF .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 2004, 78 (02) :327-332
[9]   Catalase activity in cerebellum, hippocampus, frontal cortex and striatum after status epilepticus induced by pilocarpine in Wistar rats [J].
Freitas, RM ;
Nascimento, VS ;
Vasconcelos, SMM ;
Sousa, FCF ;
Viana, GSB ;
Fonteles, MMF .
NEUROSCIENCE LETTERS, 2004, 365 (02) :102-105
[10]  
Huong NTT, 1998, BIOL PHARM BULL, V21, P978, DOI 10.1248/bpb.21.978