Gene expression regulation of Bcl2, Bax and cytochrome-C by geraniol on chronic MPTP/probenecid induced C57BL/6 mice model of Parkinson's disease

被引:48
|
作者
Rekha, Karamkolly R. [1 ]
Selvakumar, Govindasamy P. [2 ]
机构
[1] Annamalai Univ, Raja Muthaiah Med Coll, Fac Med, Div Biochem, Annamalainagar 608002, Tamil Nadu, India
[2] Annamalai Univ, Fac Sci, Dept Biochem & Biotechnol, Annamalainagar 608002, Tamil Nadu, India
关键词
Parkinson's disease; MPTP; Geraniol; Neuroprotective; Apoptosis; DOPAMINERGIC-NEURONS; APOPTOTIC DEATH; MOLECULAR PATHWAYS; OXIDATIVE STRESS; MOUSE MODEL; MPTP; NEUROTOXICITY; MITOCHONDRIA; ANTIOXIDANT; ACTIVATION;
D O I
10.1016/j.cbi.2014.04.010
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
Parkinson's disease (PD) is a common disabling movement disorder owing to progressive depletion of dopamine in nigrostriatal region, and can be experimentally accelerated by the neurotoxin 1-methyl4-phenyl-1, 2, 3, 6-tetrahydropyridine (MPTP). MPTP-treated mice are a representative animal model for searching for the therapeutic agents for PD without adverse effect. In this study we investigated the effect of geraniol (GE) on chronic MPTP/probenecid (MPTP/p) induced apoptotic changes in nigrostriatal region. We observed that chronic exposure to MPTP/p led to increased expression of apoptotic markers, results in neurodegeneration and motor behavioral impairments in mice. Pretreatment with GE to MPTP/p significantly improved motor functions and ameliorated striatal antioxidant balance. In addition, GE attenuated the expression of apoptotic markers evident by the normalized Bcl-2/Bax ratio and decreased expression of cytochrome-C and caspase-9 in the substantia nigra and striatum of MPTP/p induced mice model of PD. The findings of the present study suggested that GE, a new therapeutic potential avenue may have beneficial effects in slowing or preventing the progression of PD and other neurodegenerative disorders. (C) 2014 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:57 / 66
页数:10
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