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Synergistic Neuroprotective Effects of Two Herbal Ingredients via CREB-Dependent Pathway
As two natural oligosaccharide esters, 3,6’-Disinapoyl sucrose (DISS) and tenuifolisideA (TFSA) are originating from the root of Polygala tenuifolia Willd, a traditional Chinese medicine used in treatment of mental disorders. Previous reports have shown that both of them possess in vitro neuroprotec...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5037165/ https://www.ncbi.nlm.nih.gov/pubmed/27729863 http://dx.doi.org/10.3389/fphar.2016.00337 |
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author | Liu, Xu Wang, Dongxiao Zhao, Runqing Dong, Xianzhe Hu, Yuan Liu, Ping |
author_facet | Liu, Xu Wang, Dongxiao Zhao, Runqing Dong, Xianzhe Hu, Yuan Liu, Ping |
author_sort | Liu, Xu |
collection | PubMed |
description | As two natural oligosaccharide esters, 3,6’-Disinapoyl sucrose (DISS) and tenuifolisideA (TFSA) are originating from the root of Polygala tenuifolia Willd, a traditional Chinese medicine used in treatment of mental disorders. Previous reports have shown that both of them possess in vitro neuroprotective effects by stimulating different upstream pathways related with cyclic AMP-responsive element-binding protein (CREB). In the present study, we investigated the additive neuroprotective effects of DISS and TFSA on Glu-induced damage of SY5Y cells and purposed the possible underlying mechanism. The interaction between DISS and TFSA showed a clear-cut synergistic effect as evidenced by combination index (CI). Additional evidence from biochemical (NOS activity) assays confirmed their additive inhibition on the Glu-induced NOS hyperactivation. Moreover, we showed that co-treatment of DISS and TFSA resulted in an additively up-regulated phosphorylation of CREB as well as increased expressions of CRTC1 and BDNF. Neuroprotective effects of DISS and TFSA on Glu-induced decrease in cell viability were blocked by MAPK/ERK1/2 inhibitor (U0126) and PI3-K inhibitor (LY290042). Nevertheless, the CRTC1 or BDNF expression induced by these two compounds was significantly reduced in the presence of either ERK or PI3-K inhibitor, indicating that the two oligosaccharide esters shared some common pathways in the regulation of CREB-BDNF pathway. Taken together, we, for the first time, showed that DISS and TFSA exerted the additive neuroprotective effects on CREB-BDNF signaling pathway through complementary mechanisms. |
format | Online Article Text |
id | pubmed-5037165 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-50371652016-10-11 Synergistic Neuroprotective Effects of Two Herbal Ingredients via CREB-Dependent Pathway Liu, Xu Wang, Dongxiao Zhao, Runqing Dong, Xianzhe Hu, Yuan Liu, Ping Front Pharmacol Pharmacology As two natural oligosaccharide esters, 3,6’-Disinapoyl sucrose (DISS) and tenuifolisideA (TFSA) are originating from the root of Polygala tenuifolia Willd, a traditional Chinese medicine used in treatment of mental disorders. Previous reports have shown that both of them possess in vitro neuroprotective effects by stimulating different upstream pathways related with cyclic AMP-responsive element-binding protein (CREB). In the present study, we investigated the additive neuroprotective effects of DISS and TFSA on Glu-induced damage of SY5Y cells and purposed the possible underlying mechanism. The interaction between DISS and TFSA showed a clear-cut synergistic effect as evidenced by combination index (CI). Additional evidence from biochemical (NOS activity) assays confirmed their additive inhibition on the Glu-induced NOS hyperactivation. Moreover, we showed that co-treatment of DISS and TFSA resulted in an additively up-regulated phosphorylation of CREB as well as increased expressions of CRTC1 and BDNF. Neuroprotective effects of DISS and TFSA on Glu-induced decrease in cell viability were blocked by MAPK/ERK1/2 inhibitor (U0126) and PI3-K inhibitor (LY290042). Nevertheless, the CRTC1 or BDNF expression induced by these two compounds was significantly reduced in the presence of either ERK or PI3-K inhibitor, indicating that the two oligosaccharide esters shared some common pathways in the regulation of CREB-BDNF pathway. Taken together, we, for the first time, showed that DISS and TFSA exerted the additive neuroprotective effects on CREB-BDNF signaling pathway through complementary mechanisms. Frontiers Media S.A. 2016-09-27 /pmc/articles/PMC5037165/ /pubmed/27729863 http://dx.doi.org/10.3389/fphar.2016.00337 Text en Copyright © 2016 Liu, Wang, Zhao, Dong, Hu and Liu. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Pharmacology Liu, Xu Wang, Dongxiao Zhao, Runqing Dong, Xianzhe Hu, Yuan Liu, Ping Synergistic Neuroprotective Effects of Two Herbal Ingredients via CREB-Dependent Pathway |
title | Synergistic Neuroprotective Effects of Two Herbal Ingredients via CREB-Dependent Pathway |
title_full | Synergistic Neuroprotective Effects of Two Herbal Ingredients via CREB-Dependent Pathway |
title_fullStr | Synergistic Neuroprotective Effects of Two Herbal Ingredients via CREB-Dependent Pathway |
title_full_unstemmed | Synergistic Neuroprotective Effects of Two Herbal Ingredients via CREB-Dependent Pathway |
title_short | Synergistic Neuroprotective Effects of Two Herbal Ingredients via CREB-Dependent Pathway |
title_sort | synergistic neuroprotective effects of two herbal ingredients via creb-dependent pathway |
topic | Pharmacology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5037165/ https://www.ncbi.nlm.nih.gov/pubmed/27729863 http://dx.doi.org/10.3389/fphar.2016.00337 |
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