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Chinese Herbal Complex ‘Bu Shen Jie Du Fang' (BSJDF) Modulated Autophagy in an MPP(+)-Induced Cell Model of Parkinson's Disease
Autophagy plays an important role in the development of Parkinson disease (PD). Previous studies showed that autophagy could protect cells from α-synuclein toxicity and promote functional coupling of mitochondria. But it is still a question whether modulating autophagy can be used to treat PD. In tr...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6436328/ https://www.ncbi.nlm.nih.gov/pubmed/31001356 http://dx.doi.org/10.1155/2019/8920813 |
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author | Liu, Cuifang Huang, Xiaobo Qiu, Shengxiang Chen, Wenqiang Li, Weihong Zhang, Haiyan Wang, Tao Wang, Xue Wu, Xiling |
author_facet | Liu, Cuifang Huang, Xiaobo Qiu, Shengxiang Chen, Wenqiang Li, Weihong Zhang, Haiyan Wang, Tao Wang, Xue Wu, Xiling |
author_sort | Liu, Cuifang |
collection | PubMed |
description | Autophagy plays an important role in the development of Parkinson disease (PD). Previous studies showed that autophagy could protect cells from α-synuclein toxicity and promote functional coupling of mitochondria. But it is still a question whether modulating autophagy can be used to treat PD. In traditional Chinese medicine, a specific Chinese herbal complex called Bu Shen Jie Du Fang (BSJDF) has a long history of treating motor impairments similar to Parkinson disease, while its mechanism is still unclear. As a pilot study, we aimed to evaluate the efficacy and its mechanism of Bu Shen Jie Du Fang in an MPP(+)-induced cell model of Parkinson's disease. And the phase contrast microscope (PCM) revealed that the BSJDF group had the greatest surviving cell counts compared with all other treated cell groups except the normal group. And Cell Counting Kit 8 (CCK8) assays showed a similar result. In BSJDF group, 3.7 ×10(7) cells/dish was identified by hemocytometer counts, which was significantly higher than other groups except the normal cells (p<0.05). In the BSJDF group, autophagy can be observed by transmission electron microscopy (TEM). Protein expression of Atg12 and LC3 in the BSJDF group was upregulated compared to the PD model group (p<0.05). Atg12 mRNA expression was also upregulated in the BSJDF group (p<0.05). In conclusion, our study indicated that the therapeutic mechanisms of BSJDF may be mediated by stimulating autophagy, and modulating autophagy can be used to treat PD. |
format | Online Article Text |
id | pubmed-6436328 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-64363282019-04-18 Chinese Herbal Complex ‘Bu Shen Jie Du Fang' (BSJDF) Modulated Autophagy in an MPP(+)-Induced Cell Model of Parkinson's Disease Liu, Cuifang Huang, Xiaobo Qiu, Shengxiang Chen, Wenqiang Li, Weihong Zhang, Haiyan Wang, Tao Wang, Xue Wu, Xiling Evid Based Complement Alternat Med Research Article Autophagy plays an important role in the development of Parkinson disease (PD). Previous studies showed that autophagy could protect cells from α-synuclein toxicity and promote functional coupling of mitochondria. But it is still a question whether modulating autophagy can be used to treat PD. In traditional Chinese medicine, a specific Chinese herbal complex called Bu Shen Jie Du Fang (BSJDF) has a long history of treating motor impairments similar to Parkinson disease, while its mechanism is still unclear. As a pilot study, we aimed to evaluate the efficacy and its mechanism of Bu Shen Jie Du Fang in an MPP(+)-induced cell model of Parkinson's disease. And the phase contrast microscope (PCM) revealed that the BSJDF group had the greatest surviving cell counts compared with all other treated cell groups except the normal group. And Cell Counting Kit 8 (CCK8) assays showed a similar result. In BSJDF group, 3.7 ×10(7) cells/dish was identified by hemocytometer counts, which was significantly higher than other groups except the normal cells (p<0.05). In the BSJDF group, autophagy can be observed by transmission electron microscopy (TEM). Protein expression of Atg12 and LC3 in the BSJDF group was upregulated compared to the PD model group (p<0.05). Atg12 mRNA expression was also upregulated in the BSJDF group (p<0.05). In conclusion, our study indicated that the therapeutic mechanisms of BSJDF may be mediated by stimulating autophagy, and modulating autophagy can be used to treat PD. Hindawi 2019-03-13 /pmc/articles/PMC6436328/ /pubmed/31001356 http://dx.doi.org/10.1155/2019/8920813 Text en Copyright © 2019 Cuifang Liu et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Liu, Cuifang Huang, Xiaobo Qiu, Shengxiang Chen, Wenqiang Li, Weihong Zhang, Haiyan Wang, Tao Wang, Xue Wu, Xiling Chinese Herbal Complex ‘Bu Shen Jie Du Fang' (BSJDF) Modulated Autophagy in an MPP(+)-Induced Cell Model of Parkinson's Disease |
title | Chinese Herbal Complex ‘Bu Shen Jie Du Fang' (BSJDF) Modulated Autophagy in an MPP(+)-Induced Cell Model of Parkinson's Disease |
title_full | Chinese Herbal Complex ‘Bu Shen Jie Du Fang' (BSJDF) Modulated Autophagy in an MPP(+)-Induced Cell Model of Parkinson's Disease |
title_fullStr | Chinese Herbal Complex ‘Bu Shen Jie Du Fang' (BSJDF) Modulated Autophagy in an MPP(+)-Induced Cell Model of Parkinson's Disease |
title_full_unstemmed | Chinese Herbal Complex ‘Bu Shen Jie Du Fang' (BSJDF) Modulated Autophagy in an MPP(+)-Induced Cell Model of Parkinson's Disease |
title_short | Chinese Herbal Complex ‘Bu Shen Jie Du Fang' (BSJDF) Modulated Autophagy in an MPP(+)-Induced Cell Model of Parkinson's Disease |
title_sort | chinese herbal complex ‘bu shen jie du fang' (bsjdf) modulated autophagy in an mpp(+)-induced cell model of parkinson's disease |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6436328/ https://www.ncbi.nlm.nih.gov/pubmed/31001356 http://dx.doi.org/10.1155/2019/8920813 |
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