S-Allylcysteine, a garlic compound, protects against oxidative stress in 1-methyl-4-phenylpyridinium-induced parkinsonism in mice

被引:44
|
作者
Rojas, Patricia [1 ]
Serrano-Garcia, Norma [1 ]
Medina-Campos, Omar N. [2 ]
Pedraza-Chaverri, Jose [2 ]
Maldonado, Perla D. [3 ]
Ruiz-Sanchez, Elizabeth [1 ]
机构
[1] Natl Inst Neurol & Neurosurg, Lab Neurotoxicol, Mexico City 14269, DF, Mexico
[2] Univ Nacl Autonoma Mexico, Dept Biol, Fac Chem, Mexico City 04510, DF, Mexico
[3] Natl Inst Neurol & Neurosurg, Lab Cerebral Vasc Pathol, Mexico City 14269, DF, Mexico
来源
JOURNAL OF NUTRITIONAL BIOCHEMISTRY | 2011年 / 22卷 / 10期
关键词
Parkinson's disease; 1-methyl-4-phenylpyridinium; S-Allylcysteine; Dopamine; Neuroprotection; Antioxidant defense; LIPID-PEROXIDATION; ENDOTHELIAL-CELLS; IN-VITRO; ANTIOXIDANT; MPTP; EXTRACT; RAT; PREVENTS; OXYGEN; MPP+;
D O I
10.1016/j.jnutbio.2010.08.005
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
S-Allylcysteine (SAC), the most abundant organosulfur compound in aged garlic extract, has multifunctional activity via different mechanisms and neuroprotective effects that are exerted probably via its antioxidant or free radical scavenger action. The 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine-treated mouse has been the most widely used model for assessing neuroprotective agents for Parkinson's disease. 1-Methyl-4-phenylpyridinium (MPP+) is the stable metabolite of 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine, and it causes nigrostriatal dopaminergic neurotoxicity. Previous studies suggest that oxidative stress, via free radical production, is involved in MPP+-induced neurotoxicity. Here, we report on the neuroprotective effect of SAC against oxidative stress induced by MPP+ in the striatum of C57BL/6J mice. Mice were pretreated with SAC (125 mg/kg ip) daily for 17 days, followed by administration of MPP+ (0.72 mg/kg icv), and were sacrificed 24 h later to evaluate lipid peroxidation, different antioxidant enzyme activities, spontaneous locomotor activity and dopamine (DA) content. MPP+ administration resulted in a significant decrease in DA levels in the striatum. Mice receiving SAC (125 mg/kg ip) had significantly attenuated MPP+-induced loss of striatal DA levels (32%). The neuroprotective effect of SAC against MPP+ neurotoxicity was associated with blocked (100% of protection) of lipid peroxidation and reduction of superoxide radical production indicated by an up-regulation of Cu-Zn-superoxide dismutase activity - both of which are indices of oxidative stress. Behavioral analyses showed that SAC improved MPP+-induced impairment of locomotion (35%). These findings suggest that in mice, SAC attenuates MPP+-induced neurotoxicity in the striatum and that an antioxidant effect against oxidative stress may be partly responsible for its observed neuroprotective effects. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:937 / 944
页数:8
相关论文
共 50 条
  • [1] Combination of S-allylcysteine and lycopene protects against N-methyl-N′-nitro-N-nitrosoguanidine-induced genotoxicity and oxidative stress in mice
    Velmurugan, B
    Mohan, KVPC
    Abraham, SK
    Nagini, S
    [J]. NUTRITION RESEARCH, 2005, 25 (06) : 577 - 586
  • [2] Glia Maturation Factor Deficiency Suppresses 1-Methyl-4-Phenylpyridinium-Induced Oxidative Stress in Astrocytes
    Khan, Mohammad Moshahid
    Kempuraj, Duraisamy
    Zaheer, Smita
    Zaheer, Asgar
    [J]. JOURNAL OF MOLECULAR NEUROSCIENCE, 2014, 53 (04) : 590 - 599
  • [3] Glia Maturation Factor Deficiency Suppresses 1-Methyl-4-Phenylpyridinium-Induced Oxidative Stress in Astrocytes
    Mohammad Moshahid Khan
    Duraisamy Kempuraj
    Smita Zaheer
    Asgar Zaheer
    [J]. Journal of Molecular Neuroscience, 2014, 53 : 590 - 599
  • [4] Activation of α7 Nicotinic Acetylcholine Receptor Protects Against 1-Methyl-4-Phenylpyridinium-Induced Astroglial Apoptosis
    Hua, Ye
    Yang, Beibei
    Chen, Qiang
    Zhang, Ji
    Hu, Jun
    Fan, Yi
    [J]. FRONTIERS IN CELLULAR NEUROSCIENCE, 2019, 13
  • [5] Overexpression of Heme Oxygenase-1 Protects Dopaminergic Neurons against 1-Methyl-4-Phenylpyridinium-Induced Neurotoxicity
    Hung, Shih-Ya
    Liou, Houng-Chi
    Kang, Kai-Hsiang
    Wu, Ruey-Meei
    Wen, Chun-Chiang
    Fu, Wen-Mei
    [J]. MOLECULAR PHARMACOLOGY, 2008, 74 (06) : 1564 - 1575
  • [6] MicroRNA-7 Protects against 1-Methyl-4-Phenylpyridinium-Induced Cell Death by Targeting RelA
    Choi, Doo Chul
    Chae, Yoon-Jee
    Kabaria, Savan
    Chaudhuri, Amrita Datta
    Jain, Mohit Raja
    Li, Hong
    Mouradian, M. Maral
    Junn, Eunsung
    [J]. JOURNAL OF NEUROSCIENCE, 2014, 34 (38): : 12725 - 12737
  • [7] Chemoprotection against N-methyl-N′-nitro-N- nitrosoguanidine-induced oxidative stress by S-allylcysteine, a garlic constituent, in Wistar rats
    Velmurugan, B
    Subapriya, R
    Nagini, S
    [J]. TOXICOLOGY MECHANISMS AND METHODS, 2003, 13 (02) : 83 - 87
  • [8] Fenamate protects against 1-methyl-4-phenylpyridinium-induced apoptosis in dopaminergic MN9D cells
    Viet Le
    Mapa, Mapa
    Wimalasena, Kandatege
    [J]. ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2018, 256
  • [9] Raf kinase inhibitor protein protects microglial cells against 1-methyl-4-phenylpyridinium-induced neuroinflammation in vitro
    Gao, Yuanlin
    Zhong, Jie
    Jiang, Lei
    [J]. EXPERIMENTAL CELL RESEARCH, 2018, 372 (02) : 108 - 117
  • [10] S-allylcysteine prevents cisplatin-induced nephrotoxicity and oxidative stress
    Gomez-Sierra, Tania
    Molina-Jijon, Eduardo
    Tapia, Edilia
    Hernandez-Pando, Rogelio
    Ramses Garcia-Nino, Wylly
    Maldonado, Perla D.
    Luis Reyes, Jose
    Barrera-Oviedo, Diana
    Torres, Ismael
    Pedraza-Chaverri, Jose
    [J]. JOURNAL OF PHARMACY AND PHARMACOLOGY, 2014, 66 (09) : 1271 - 1281