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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.
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页码:57 / 66
页数:10
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