EGb761 blocks MPP+-induced lipid peroxidation in mouse corpus striatum

被引:31
作者
Rojas, P
Garduño, B
Rojas, C
Vigueras, RM
Rojas-Castañeda, J
Ríos, C
Serrano-Garcia, N
机构
[1] Inst Nacl Neurol & Neurocirug, Lab Neurotoxicol, Manuel Velasco Suarez SS, Mexico City 14269, DF, Mexico
[2] Univ Nacl Autonoma Mexico, Dept Physiol, Inst Invest Biomed, Mexico City 04510, DF, Mexico
[3] Inst Nacl Pediat, Lab Histomorphol, Mexico City 04530, DF, Mexico
[4] Inst Nacl Neurol & Neurocirug, Dept Neurochem, Manuel Velasco Suarez SS, Mexico City 14269, DF, Mexico
关键词
MPP+; lipid peroxidation; neuroprotection; Parkinson's disease; EGb761;
D O I
10.1023/A:1013971524150
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
EGb761 has been suggested to be an antioxidant and free radical scavenger. Excess generation of free radicals, leading to lipid peroxidation (LP), has been proposed to play a role in the damage to striatal neurons induced by 1-methyl-4-phenylpyridinium (MPP+). We investigated the effects of EGb761 pretreatment on MPP+ neurotoxicity. C-57 black mice were pretreated with EGb761 for 17 days at different doses (0.63, 1.25, 2.5, 5 or 10 mg/kg) followed by administration of MPP+, (0.18, 0.36 or 0.72 mg/kg). LP was analyzed in corpus striatum at 30 min, 1 h, 2 h and 24 h after MPP+ administration. Striatal dopamine content was analyzed by HPLC at the highest EGb761 dose at 2 h and 24 It after MPP+ administration. MPP+-induced LP was blocked (100%) by EGb761 (10 mg/kg). Pretreatment with EGb761 partially prevented (32%) the dopamine-depleting effect of MPP+ at 24 h. These results suggest that supplements of EGb761 may be effective at preventing MPP+-induced oxidative stress.
引用
收藏
页码:1245 / 1251
页数:7
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