Neuroprotective effect of modified Chungsimyeolda-tang, a traditional Korean herbal formula, via autophagy induction in models of Parkinson's disease

被引:17
作者
Bae, Nayoung [1 ,2 ]
Chung, Sungkwon [3 ]
Kim, Hee Ju [1 ]
Cha, Jin Wook [1 ]
Oh, Hyungun [3 ]
Gu, Ming-Yao [1 ]
Oh, Myung Sook [4 ,5 ]
Yang, Hyun Ok [1 ]
机构
[1] Korea Inst Sci & Technol, Nat Prod Res Ctr, Kangnung 210340, Gangwon Do, South Korea
[2] Pusan Natl Univ, Sch Korean Med, Dept Sasang Constitut Med, Yangsan 626870, South Korea
[3] Sungkyunkwan Univ, Sch Med, Samsung Biomed Res Inst, Dept Physiol, Suwon 440746, South Korea
[4] Kyung Hee Univ, Dept Life & Nanopharrnaceut Sci, Seoul 130701, South Korea
[5] Kyung Hee Univ, Kyung Hee East West Pharmaceut Res Inst, Seoul 130701, South Korea
基金
新加坡国家研究基金会;
关键词
DG; Parkinson's disease; Neuroprotection; Autophagy; Lactacystin; PC12; cells; CHAPERONE-MEDIATED AUTOPHAGY; POLYGALA-TENUIFOLIA WILLD; ALPHA-SYNUCLEIN; 1-METHYL-4-PHENYL-1,2,3,6-TETRAHYDROPYRIDINE MPTP; CELL-DEATH; PROTEASOME; INHIBITION; NEUROTOXIN; BRAIN; HEPATOCYTES;
D O I
10.1016/j.jep.2014.11.007
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Aim of the study: Previous studies in our laboratory revealed the neuroprotective effect of modified Yeoldahanso-tang (MYH) in models of Parkinson's disease (PD). In this study, we investigated another traditional Korean herbal formula, modified Chungsimyeolda-tang (termed DG), as a potential treatment for PD. Chungsimyeolda-tang has been used in Korea to treat cerebrovascular diseases, such as stroke. Here, we verify the neuroprotective and autophagy-inducing effects of DG to evaluate any potential anti-parkinsonian properties. Materials and methods: 1-Methyl-4-phenylpyridinium (MPP+) and rotenone were used to induce cytotoxicity in nerve growth factor (NGF)-differentiated rat pheochromocytoma (PC12) cells. Cell viability was measured using an MTT assay. Induction of autophagy by DG in NGF-differentiated PC12 cells was measured using an immunoblotting assay with an LC3 antibody. The proteasomal inhibitor lactacystin was used to induce ubiquitin-proteasome system (UPS) dysfunction in NGF-differentiated PC12 cells. DG-mediated clearance of aggregated proteins was measured using an immunoblotting assay with a ubiquitin antibody. Results and conclusions: Our findings indicate that DG robustly protects NGF-differentiated PC12 cells against the neurotoxic effects of MPP+ and rotenone in an in vitro model. Furthermore, DG protects NGFdifferentiated PC12 cells against lactacystin-induced cell death. This effect is partially mediated by an increased autophagy associated with the enhanced degradation of aggregated proteins. This study suggests that DG is an attractive candidate drug for inducing autophagy and, therefore, may represent a promising strategy to prevent diseases associated with misfolded/aggregated proteins in various neurodegenerative disorders, including Parkinson's disease. (C) 2014 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:93 / 101
页数:9
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