Cassiae semen, a seed of Cassia obtusifolia, has neuroprotective effects in Parkinson's disease models

被引:95
作者
Ju, Mi Sun [1 ]
Kim, Hyo Geun [1 ]
Choi, Jin Gyu [1 ]
Ryu, Jong Hoon [1 ,2 ,3 ]
Hur, Jinyoung [4 ]
Kim, Youn Jung [5 ]
Oh, Myung Sook [1 ,2 ,3 ]
机构
[1] Kyung Hee Univ, Dept Oriental Pharmaceut Sci, Coll Pharm, Seoul 130701, South Korea
[2] Kyung Hee Univ, Dept Life & Nanopharmaceut Sci, Seoul 130701, South Korea
[3] Kyung Hee Univ, Kyung Hee EW Pharmaceut Res Inst, Seoul 130701, South Korea
[4] Kyung Hee Univ, Brain Korea Project Ctr 21, Sch Med, Seoul 130701, South Korea
[5] Kyung Hee Univ, Coll Nursing Sci, EW Nursing Res Inst, Seoul 130701, South Korea
关键词
Cassiae semen; Parkinson's disease; 6-Hydroxydopamine; 1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine; SCUTELLARIA-BAICALENSIS GEORGI; OXIDATIVE STRESS; NEURODEGENERATIVE DISORDERS; DOPAMINERGIC-NEURONS; MPTP; NEUROTOXICITY; MECHANISM; 6-HYDROXYDOPAMINE; PATHOGENESIS; GLUTATHIONE;
D O I
10.1016/j.fct.2010.05.002
中图分类号
TS2 [食品工业];
学科分类号
100403 [营养与食品卫生学];
摘要
Cassiae semen, a commonly consumed tea and medicinal food, has been shown to have multiple therapeutic actions related to the prevention of dementia and ischemia. In this study, we investigated the effects of extract of Cassiae semen (COE) against neurotoxicities in in vitro and in vivo Parkinson's disease (PD) models. In PC12 cells, COE attenuated the cell damage induced by 100 mu M 6-hydroxydopamine (6-OHDA) stress in MTT assay, and it inhibited the overproduction of reactive oxygen species, glutathione depletion, mitochondrial membrane depolarization and caspase-3 activation at 0.1-10 mu g/ml. In addition. COE showed radical scavenging activity in the DPPH and ABTS assays. In mesencephalic dopaminergic (DA) culture, COE protected DA cells against 10 mu M 6-OHDA- and 10 mu M 1-methyl-4-phenylpyridine-induced toxicities at 0.1-1 mu g/ml. We also evaluated the effect of COE in a mouse PD model induced by 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP). In the pole test, COE (50 mg/kg, 15 days) + MPTP (30 mg/kg. 5 days)-treated group had decreased T-turn and T-LA which were longer in MPTP group. Moreover, COE significantly protected DA neuronal degeneration induced by MPTP in the substantia nigra and striatum of these mice. These results demonstrate that COE can prevent DA neurons against the toxicities involved in PD. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2037 / 2044
页数:8
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