Mulberry fruit protects dopaminergic neurons in toxin-induced Parkinson's disease models

被引:123
作者
Kim, Hyo Geun [1 ,2 ]
Ju, Mi Sun [1 ,2 ]
Shim, Jin Sup [1 ,2 ]
Kim, Min Cheol [3 ]
Lee, Sang-Hun [4 ]
Huh, Youngbuhm [5 ]
Kim, Sun Yeou [3 ]
Oh, Myung Sook [1 ,2 ]
机构
[1] Kyung Hee Univ, Dept Oriental Pharmaceut Sci, Seoul 130701, South Korea
[2] Kyung Hee Univ, Kyung Hee EW Pharmaceut Res Inst, Coll Pharm, Seoul 130701, South Korea
[3] Kyung Hee Univ, Grad Sch EW Med Sci, Yongin 449701, South Korea
[4] Hanyang Univ, Dept Biochem, Coll Med, Seoul 133791, South Korea
[5] Kyung Hee Univ, Dept Anat & Neurobiol, Coll Med, Seoul 130701, South Korea
关键词
Mulberry fruit; Parkinson's disease; Neuroprotective effects; 6-Hydroxydopamine; 1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine; BLUEBERRY SUPPLEMENTED DIET; BEHAVIORAL DEFICITS; SIGNAL-TRANSDUCTION; ANTHOCYANINS; STRAWBERRY; APOPTOSIS; 6-HYDROXYDOPAMINE; POLYPHENOLICS; MECHANISMS; CASPASES;
D O I
10.1017/S0007114510000218
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Parkinson's disease (PD), one of the most common neurodegenerative disorders, is characterised by the loss of dopaminergic neurons in the substantia nigra pars compacta (SNpc) to the striatum (ST), and involves oxidative stress. Mulberry fruit from Morus alba L. (Moraceae) is commonly eaten, and has long been used in traditional oriental medicine. It contains well-known antioxidant agents such as anthocyanins. The present study examined the protective effects of 70% ethanol extract of mulberry fruit (ME) against neurotoxicity in in vitro and in vivo PD models. In SH-SY5Y cells stressed with 6-hydroxydopamine (6-OHDA), ME significantly protected the cells from neurotoxicity in a dose-dependent manner. Other assays demonstrated that the protective effect of ME was mediated by its antioxidant and anti-apoptotic effects, regulating reactive oxygen species and NO generation, Bcl-2 and Bax proteins, mitochondrial membrane depolarisation and caspase-3 activation. In mesencephalic primary cells stressed with 6-OHDA or 1-methy1-4-phenylpyridinium (MPP+), pre-treatment with ME also protected dopamine neurons, showing a wide range of effective concentrations in MPP+-induced toxicity. In the sub-acute mouse PD model induced by 1-methyl-4-phenyl-1,2,3, 6-tetrahydropyridine (MPTP), ME showed a preventative effect against PD-like symptoms (bradykinesia) in the behavioural test and prevented MPTP-induced dopaminergic neuronal damage in an immunocytochemical analysis of the SNpc and ST. These results indicate that ME has neuroprotective effects in in vitro and in vivo PD models, and that it may be useful in preventing or treating PD.
引用
收藏
页码:8 / 16
页数:9
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