Antioxidant effect of nimodipine in young rats after pilocarpine-induced seizures

被引:18
作者
Nascimento, VS [1 ]
D'alva, MS [1 ]
Oliveira, AA [1 ]
Freitas, RM [1 ]
Vasconcelos, SMM [1 ]
Sousa, FCF [1 ]
Fonteles, MMF [1 ]
机构
[1] Univ Fed Ceara, Sch Med, Neuropharmacol Lab, Dept Physiol & Pharmacol, BR-60431270 Fortaleza, Ceara, Brazil
关键词
nimodipine; pilocarpine; striatum; lipid peroxidation; catalase;
D O I
10.1016/j.pbb.2005.07.001
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
Nimodipine (ND) is a centrally active calcium antagonist that blocks the voltage-dependent L-type channels. Its antiepileptic properties have been proved in various animal models, including pilocarpine-induced seizures in adult rats. In order to investigate protective effects of the ND (10 (ND10) and 30 mg/kg (ND30), i.p.), young mate rats (21-day-old) received ND injections before pilocarpine administration (400 mg/kg, s.c., pilocarpine group (P400)). The pretreatment with ND 10 and ND30 prolonged the latencies of seizures and death on this seizure model. ND pretreatment in two doses decreased the levels of lipid peroxidation when compared to pilocarpine group. The P400 administration increased the striatal catalase activity. However, the administration of ND, in dose of 30 mg/kg, 30 min before pilocarpine, preserved catalase activity in normal levels. Oil the other hand, no change was detected in the animals treated with the dose of 10 mg/kg. Our results confirm the neuroprotective effect of ND on the seizures in Young rats, suggesting that this drug acts positively on lipid peroxidation. Our observations shows that nimodipine cannot induces these effects via blockade of Ca2+-channel. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:11 / 16
页数:6
相关论文
共 46 条
[1]  
Aicardi J, 1983, Adv Neurol, V34, P115
[2]  
AZMITIA EC, 1993, DRUG DEV, V2, P437
[3]   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
[4]   KAINIC ACID-INDUCED SEIZURES AND BRAIN-DAMAGE IN THE RAT - ROLE OF CALCIUM HOMEOSTASIS [J].
BERG, M ;
BRUHN, T ;
FRANDSEN, A ;
SCHOUSBOE, A ;
DIEMER, NH .
JOURNAL OF NEUROSCIENCE RESEARCH, 1995, 40 (05) :641-646
[5]   THE PILOCARPINE MODEL OF EPILEPSY [J].
CAVALHEIRO, EA .
ITALIAN JOURNAL OF NEUROLOGICAL SCIENCES, 1995, 16 (1-2) :33-37
[6]   ASSAY OF CATALASES AND PEROXIDASES [J].
CHANCE, B ;
MAEHLY, AC .
METHODS IN ENZYMOLOGY, 1955, 2 :764-775
[7]  
CHARKRABARTI A, 1998, BRAIN RES B, V45, P495
[8]  
Costa L G:., 1994, Principles of neurotoxicology, P475
[9]   Attenuating effects of melatonin on pilocarpine-induced seizures in rats [J].
Costa-Lotufo, LV ;
Fonteles, MMD ;
Lima, ISP ;
de Oliveira, AA ;
Nascimento, VS ;
de Bruin, VMS ;
Viana, GSB .
COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY C-TOXICOLOGY & PHARMACOLOGY, 2002, 131 (04) :521-529
[10]   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