Neuroprotective Effect ofCoptis chinensisin MPP+ and MPTP-Induced Parkinson’s Disease Models

黄连 黄连 黄连碱 MPTP公司 小檗碱 神经保护 药理学 传统医学 巴马汀 氧化应激 生物碱 医学 帕金森病 生物 疾病 中医药 植物 内科学 病理 替代医学
作者
Thomas Friedemann,Yue Ying,Weigang Wang,Edgar R. Kramer,Udo Schumacher,Jian Fei,Sven Schröder
出处
期刊:The American Journal of Chinese Medicine [World Scientific]
卷期号:44 (05): 907-925 被引量:33
标识
DOI:10.1142/s0192415x16500506
摘要

The rhizome of Coptis chinensis is commonly used in traditional Chinese medicine alone or in combination with other herbs to treat diseases characterized by causing oxidative stress including inflammatory diseases, diabetes mellitus and neurodegenerative diseases. In particular, there is emerging evidence that Coptis chinensis is effective in the treatment of neurodegenerative diseases associated with oxidative stress. Hence, the aim of this study was to investigate the neuroprotective effect of Coptis chinensis in vitro and in vivo using MPP[Formula: see text] and MPTP models of Parkinson’s disease. MPP[Formula: see text] treated human SH-SY5Y neuroblastoma cells were used as a cell model of Parkinson’s disease. A 24[Formula: see text]h pre-treatment of the cells with the watery extract of Coptis chinensis significantly increased cell viability, as well as the intracellular ATP concentration and attenuated apoptosis compared to the MPP[Formula: see text] control. Further experiments with the main alkaloids of Coptidis chinensis, berberine, coptisine, jaterorrhizine and palmatine revealed that berberine and coptisine were the main active compounds responsible for the observed neuroprotective effect. However, the full extract of Coptis chinensis was more effective than the tested single alkaloids. In the MPTP-induced animal model of Parkinson’s disease, Coptis chinensis dose-dependently improved motor functions and increased tyrosine hydroxylase-positive neurons in the substantia nigra compared to the MPTP control. Based on the results of this work, Coptis chinensis and its main alkaloids could be considered potential candidates for the development of new treatment options for Parkinson’s disease.

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