Dietary Supplementation of Walnut Partially Reverses 1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine Induced Neurodegeneration in a Mouse Model of Parkinson's Disease

被引:24
作者
Essa, Musthafa Mohamed [1 ,2 ]
Subash, Selvaraju [1 ]
Dhanalakshmi, Chinnasamy [3 ]
Manivasagam, Thamilarasan [3 ]
Al-Adawi, Samir [2 ,4 ]
Guillemin, Gilles J. [5 ]
Thenmozhi, Arokiasamy Justin [3 ]
机构
[1] Sultan Qaboos Univ, CAMS, Dept Food Sci & Nutr, Muscat 123, Oman
[2] Sultan Qaboos Univ, Aging & Dementia Res Grp, Muscat, Oman
[3] Annamalai Univ, Dept Biochem & Biotechnol, Fac Sci, Annamalainagar 608002, Tamil Nadu, India
[4] Sultan Qaboos Univ, Dept Behav Med, Coll Med & Hlth Sci, Muscat, Oman
[5] Macqurie Univ, Neuropharmacol Grp, ASAM, Sydney, NSW, Australia
关键词
Walnut; Parkinson's disease; Dopamine; Antioxidants; Oxidative stress; OXIDATIVE STRESS; RAT-BRAIN; COMPLEX-I; NEUROTOXICITY; GLUTATHIONE; MELATONIN; EXTRACT; NEURONS; MICE; NUT;
D O I
10.1007/s11064-015-1593-2
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
Numerous studies indicating that natural plant sources and their active phytochemicals offer protection to the pathological processes related to the development of neurogenerative diseases including Parkinson's disease (PD). In the present study, the neuro protective efficacy of dietary supplementation of walnut (6 %) for 28 days was examined in 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) (i.p., 20 mg/kg body weight/day) for last four consecutive days. MPTP injection diminished the levels of GSH, dopamine and metabolites along with decreased activities of GPx and mitochondrial complex I. Further, the levels of TBARS and enzymatic antioxidants such as SOD and catalase, MAO-B activities were enhanced by MPTP treatment. Behavioral deficits and lowered TH expression are also proved MPTP induced neurotoxicity. Dietary supplementation of walnut attenuated MPTP-induced impairment in PD mice might be by its MAO-B inhibitory, antioxidant and mitochondrial protective actions. To find out the exact mechanism of action walnut on PD mice warrants further extensive studies.
引用
收藏
页码:1283 / 1293
页数:11
相关论文
共 61 条
[41]   Protective Effects of Walnut Extract Against Amyloid Beta Peptide-Induced Cell Death and Oxidative Stress in PC12 Cells [J].
Muthaiyah, Balu ;
Essa, Musthafa M. ;
Chauhan, Ved ;
Chauhan, Abha .
NEUROCHEMICAL RESEARCH, 2011, 36 (11) :2096-2103
[42]  
OBERLEY LW, 1984, METHOD ENZYMOL, V105, P457
[43]   Walnuts (Seeds of Juglandis sinensis L.) Protect Human Epidermal Keratinocytes against UVB-Induced Mitochondria-Mediated Apoptosis through Upregulation of ROS Elimination Pathways [J].
Park, G. ;
Kim, H. G. ;
Hong, S. -P. ;
Kim, S. Y. ;
Oh, M. S. .
SKIN PHARMACOLOGY AND PHYSIOLOGY, 2014, 27 (03) :132-140
[44]   Ropinirole protects against 1-methyl-4-phenyl-1, 2, 3, 6-tetrahydropyridine (MPTP)-induced neurotoxicity in mice via anti-apoptotic mechanism [J].
Park, Gunhyuk ;
Park, Young-Joon ;
Yang, Hyun Ok ;
Oh, Myung Sook .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 2013, 104 :163-168
[45]   Mitochondrial dysfunction in the striatum of aged chronic mouse model of Parkinson's disease [J].
Patki, Gaurav ;
Che, Yi ;
Lau, Yuen-Sum .
FRONTIERS IN AGING NEUROSCIENCE, 2009, 1
[46]   Mitochondrial dysfunction in rat brain with aging Involvement of complex I, reactive oxygen species and cardiolipin [J].
Petrosillo, G. ;
Matera, M. ;
Casanova, G. ;
Ruggiero, F. M. ;
Paradies, G. .
NEUROCHEMISTRY INTERNATIONAL, 2008, 53 (05) :126-131
[47]   Ashwagandha leaf extract: A potential agent in treating oxidative damage and physiological abnormalities seen in a mouse model of Parkinson's disease [J].
RajaSankara, Srinivasagam ;
Manivasagam, Thamilarasan ;
Surendran, Sankar .
NEUROSCIENCE LETTERS, 2009, 454 (01) :11-15
[48]  
Rajeswari A, 2006, Eur Rev Med Pharmacol Sci, V10, P157
[49]   Melatonin in walnuts: Influence on levels of melatonin and total antioxidant capacity of blood [J].
Reiter, RJ ;
Manchester, LC ;
Tan, DX .
NUTRITION, 2005, 21 (09) :920-924
[50]   A walnut diet improves endothelial function in hypercholesterolemic subjects -: A randomized crossover trial [J].
Ros, E ;
Núñez, I ;
Pérez-Heras, A ;
Serra, M ;
Gilabert, R ;
Casals, E ;
Deulofeu, R .
CIRCULATION, 2004, 109 (13) :1609-1614