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A Chinese Herbal Preparation, Xiao-Er-An-Shen Decoction, Exerts Neuron Protection by Modulation of Differentiation and Antioxidant Activity in Cultured PC12 Cells

Xiao-Er-An-Shen Decoction (XEASD), a Chinese herbal formula, has been used in clinic for treating insomnia and mental excitement in children and adolescents. However, less of scientific data supports its effectiveness in clinic. Here, we aim to study the role of XEASD in regulating neuron differenti...

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Autores principales: Li, Zhonggui, Lam, Kelly Y. C., Liu, Xiaoyan, Qi, Airong, Yao, Ping, Dong, Tina T. X., Yi, Tiegang, Tsim, Karl W. K., Chen, Jianping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5960539/
https://www.ncbi.nlm.nih.gov/pubmed/29853977
http://dx.doi.org/10.1155/2018/8670421
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author Li, Zhonggui
Lam, Kelly Y. C.
Liu, Xiaoyan
Qi, Airong
Yao, Ping
Dong, Tina T. X.
Yi, Tiegang
Tsim, Karl W. K.
Chen, Jianping
author_facet Li, Zhonggui
Lam, Kelly Y. C.
Liu, Xiaoyan
Qi, Airong
Yao, Ping
Dong, Tina T. X.
Yi, Tiegang
Tsim, Karl W. K.
Chen, Jianping
author_sort Li, Zhonggui
collection PubMed
description Xiao-Er-An-Shen Decoction (XEASD), a Chinese herbal formula, has been used in clinic for treating insomnia and mental excitement in children and adolescents. However, less of scientific data supports its effectiveness in clinic. Here, we aim to study the role of XEASD in regulating neuron differentiation and antioxidant activity. An HPLC-MS was used to chemically standardize herbal extract of XEASD. The standardized herbal extracts of XEASD (0.3–3.0 mg/mL) were applied onto cultured PC12 cells for 48 hours. The treatment with XEASD extract induced neurite outgrowth of PC12 cells in a dose-dependent manner, having the highest response by ~50% of differentiated cells. Application of XEASD extract dose dependently stimulated expressions of NF68, NF160, and NF200 in cultured PC12 cells. Furthermore, XEASD activated the phosphorylation of cAMP responsive element binding protein on PC12 cells, the effect of which was blocked by H89, a protein kinase A inhibitor. Moreover, XEASD showed free radical scavenging activity and stimulated the transcriptional activity of ARE. These results supported the neurobeneficial effects of XEASD in the induction of neurite outgrowth and protection against oxidative stress and could be useful for neurological diseases, in which neurotrophin deficiency and oxidation insult are involved.
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spelling pubmed-59605392018-05-31 A Chinese Herbal Preparation, Xiao-Er-An-Shen Decoction, Exerts Neuron Protection by Modulation of Differentiation and Antioxidant Activity in Cultured PC12 Cells Li, Zhonggui Lam, Kelly Y. C. Liu, Xiaoyan Qi, Airong Yao, Ping Dong, Tina T. X. Yi, Tiegang Tsim, Karl W. K. Chen, Jianping Evid Based Complement Alternat Med Research Article Xiao-Er-An-Shen Decoction (XEASD), a Chinese herbal formula, has been used in clinic for treating insomnia and mental excitement in children and adolescents. However, less of scientific data supports its effectiveness in clinic. Here, we aim to study the role of XEASD in regulating neuron differentiation and antioxidant activity. An HPLC-MS was used to chemically standardize herbal extract of XEASD. The standardized herbal extracts of XEASD (0.3–3.0 mg/mL) were applied onto cultured PC12 cells for 48 hours. The treatment with XEASD extract induced neurite outgrowth of PC12 cells in a dose-dependent manner, having the highest response by ~50% of differentiated cells. Application of XEASD extract dose dependently stimulated expressions of NF68, NF160, and NF200 in cultured PC12 cells. Furthermore, XEASD activated the phosphorylation of cAMP responsive element binding protein on PC12 cells, the effect of which was blocked by H89, a protein kinase A inhibitor. Moreover, XEASD showed free radical scavenging activity and stimulated the transcriptional activity of ARE. These results supported the neurobeneficial effects of XEASD in the induction of neurite outgrowth and protection against oxidative stress and could be useful for neurological diseases, in which neurotrophin deficiency and oxidation insult are involved. Hindawi 2018-05-03 /pmc/articles/PMC5960539/ /pubmed/29853977 http://dx.doi.org/10.1155/2018/8670421 Text en Copyright © 2018 Zhonggui Li 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
Li, Zhonggui
Lam, Kelly Y. C.
Liu, Xiaoyan
Qi, Airong
Yao, Ping
Dong, Tina T. X.
Yi, Tiegang
Tsim, Karl W. K.
Chen, Jianping
A Chinese Herbal Preparation, Xiao-Er-An-Shen Decoction, Exerts Neuron Protection by Modulation of Differentiation and Antioxidant Activity in Cultured PC12 Cells
title A Chinese Herbal Preparation, Xiao-Er-An-Shen Decoction, Exerts Neuron Protection by Modulation of Differentiation and Antioxidant Activity in Cultured PC12 Cells
title_full A Chinese Herbal Preparation, Xiao-Er-An-Shen Decoction, Exerts Neuron Protection by Modulation of Differentiation and Antioxidant Activity in Cultured PC12 Cells
title_fullStr A Chinese Herbal Preparation, Xiao-Er-An-Shen Decoction, Exerts Neuron Protection by Modulation of Differentiation and Antioxidant Activity in Cultured PC12 Cells
title_full_unstemmed A Chinese Herbal Preparation, Xiao-Er-An-Shen Decoction, Exerts Neuron Protection by Modulation of Differentiation and Antioxidant Activity in Cultured PC12 Cells
title_short A Chinese Herbal Preparation, Xiao-Er-An-Shen Decoction, Exerts Neuron Protection by Modulation of Differentiation and Antioxidant Activity in Cultured PC12 Cells
title_sort chinese herbal preparation, xiao-er-an-shen decoction, exerts neuron protection by modulation of differentiation and antioxidant activity in cultured pc12 cells
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5960539/
https://www.ncbi.nlm.nih.gov/pubmed/29853977
http://dx.doi.org/10.1155/2018/8670421
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