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Anti-oxidative effects of the biennial flower of Panax notoginseng against H(2)O(2)-induced cytotoxicity in cultured PC12 cells
BACKGROUND: Radix notoginseng is used in Chinese medicine to improve blood circulation and clotting; however, the pharmacological activities of other parts of Panax notoginseng have yet to be explored. The present study reports the anti-oxidative effects of various parts of Panax notoginseng. METHOD...
Autores principales: | , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2010
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2978211/ https://www.ncbi.nlm.nih.gov/pubmed/21029415 http://dx.doi.org/10.1186/1749-8546-5-38 |
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author | Choi, Roy Chi-Yan Jiang, Zhiyong Xie, Heidi Qun Cheung, Anna Wing-Han Lau, David Tai-Wai Fu, Qiang Dong, Tina Tingxia Chen, Jijun Wang, Zhengtao Tsim, Karl Wah-Keung |
author_facet | Choi, Roy Chi-Yan Jiang, Zhiyong Xie, Heidi Qun Cheung, Anna Wing-Han Lau, David Tai-Wai Fu, Qiang Dong, Tina Tingxia Chen, Jijun Wang, Zhengtao Tsim, Karl Wah-Keung |
author_sort | Choi, Roy Chi-Yan |
collection | PubMed |
description | BACKGROUND: Radix notoginseng is used in Chinese medicine to improve blood circulation and clotting; however, the pharmacological activities of other parts of Panax notoginseng have yet to be explored. The present study reports the anti-oxidative effects of various parts of Panax notoginseng. METHODS: Various parts of Panax notoginseng, including the biennial flower, stem-leaf, root-rhizome, fiber root and sideslip, were used to prepare extracts and analyzed for their anti-oxidation effects, namely suppressing xanthine oxidase activity, H(2)O(2)-induced cytotoxicity and H(2)O(2)-induced ROS formation. RESULTS: Among various parts of the herb (biennial flower, stem-leaf, root-rhizome, fiber root and sideslip), the water extract of the biennial flower showed the strongest effects in (i) inhibiting the enzymatic activity of xanthine oxidase and (ii) protecting neuronal PC12 cells against H(2)O(2)-induced cytotoxicity. Only the water extracts demonstrated such anti-oxidative effects while the ethanol extracts did not exert significant effects in suppressing xanthine oxidase and H(2)O(2)-induced neuronal cytotoxicity. CONCLUSIONS: The present study demonstrates the biennial flower of Panax notoginseng to have neuroprotection effect on cultured neurons and the underlying protection mechanism may involve anti-oxidation. |
format | Text |
id | pubmed-2978211 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-29782112010-11-11 Anti-oxidative effects of the biennial flower of Panax notoginseng against H(2)O(2)-induced cytotoxicity in cultured PC12 cells Choi, Roy Chi-Yan Jiang, Zhiyong Xie, Heidi Qun Cheung, Anna Wing-Han Lau, David Tai-Wai Fu, Qiang Dong, Tina Tingxia Chen, Jijun Wang, Zhengtao Tsim, Karl Wah-Keung Chin Med Research BACKGROUND: Radix notoginseng is used in Chinese medicine to improve blood circulation and clotting; however, the pharmacological activities of other parts of Panax notoginseng have yet to be explored. The present study reports the anti-oxidative effects of various parts of Panax notoginseng. METHODS: Various parts of Panax notoginseng, including the biennial flower, stem-leaf, root-rhizome, fiber root and sideslip, were used to prepare extracts and analyzed for their anti-oxidation effects, namely suppressing xanthine oxidase activity, H(2)O(2)-induced cytotoxicity and H(2)O(2)-induced ROS formation. RESULTS: Among various parts of the herb (biennial flower, stem-leaf, root-rhizome, fiber root and sideslip), the water extract of the biennial flower showed the strongest effects in (i) inhibiting the enzymatic activity of xanthine oxidase and (ii) protecting neuronal PC12 cells against H(2)O(2)-induced cytotoxicity. Only the water extracts demonstrated such anti-oxidative effects while the ethanol extracts did not exert significant effects in suppressing xanthine oxidase and H(2)O(2)-induced neuronal cytotoxicity. CONCLUSIONS: The present study demonstrates the biennial flower of Panax notoginseng to have neuroprotection effect on cultured neurons and the underlying protection mechanism may involve anti-oxidation. BioMed Central 2010-10-28 /pmc/articles/PMC2978211/ /pubmed/21029415 http://dx.doi.org/10.1186/1749-8546-5-38 Text en Copyright ©2010 Choi et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Choi, Roy Chi-Yan Jiang, Zhiyong Xie, Heidi Qun Cheung, Anna Wing-Han Lau, David Tai-Wai Fu, Qiang Dong, Tina Tingxia Chen, Jijun Wang, Zhengtao Tsim, Karl Wah-Keung Anti-oxidative effects of the biennial flower of Panax notoginseng against H(2)O(2)-induced cytotoxicity in cultured PC12 cells |
title | Anti-oxidative effects of the biennial flower of Panax notoginseng against H(2)O(2)-induced cytotoxicity in cultured PC12 cells |
title_full | Anti-oxidative effects of the biennial flower of Panax notoginseng against H(2)O(2)-induced cytotoxicity in cultured PC12 cells |
title_fullStr | Anti-oxidative effects of the biennial flower of Panax notoginseng against H(2)O(2)-induced cytotoxicity in cultured PC12 cells |
title_full_unstemmed | Anti-oxidative effects of the biennial flower of Panax notoginseng against H(2)O(2)-induced cytotoxicity in cultured PC12 cells |
title_short | Anti-oxidative effects of the biennial flower of Panax notoginseng against H(2)O(2)-induced cytotoxicity in cultured PC12 cells |
title_sort | anti-oxidative effects of the biennial flower of panax notoginseng against h(2)o(2)-induced cytotoxicity in cultured pc12 cells |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2978211/ https://www.ncbi.nlm.nih.gov/pubmed/21029415 http://dx.doi.org/10.1186/1749-8546-5-38 |
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