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Sodium tanshinone IIA sulfonate stimulated Cl(−) secretion in mouse trachea
Sodium tanshinone IIA sulfonate (STS) is a derivate of tanshinone IIA, a lipophilic compound in Salvia miltiorrhiza. This study aimed to investigate the effect of STS on ion transport in mouse tracheal epithelium and the mechanisms underlying it. Short-circuit current (I(sc)) was measured to evaluat...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5440052/ https://www.ncbi.nlm.nih.gov/pubmed/28542554 http://dx.doi.org/10.1371/journal.pone.0178226 |
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author | Chen, Peng-Xiao Zhang, Yi-Lin Xu, Jia-Wen Yu, Ming-Hao Huang, Jie-Hong Zhao, Lei Zhou, Wen-Liang |
author_facet | Chen, Peng-Xiao Zhang, Yi-Lin Xu, Jia-Wen Yu, Ming-Hao Huang, Jie-Hong Zhao, Lei Zhou, Wen-Liang |
author_sort | Chen, Peng-Xiao |
collection | PubMed |
description | Sodium tanshinone IIA sulfonate (STS) is a derivate of tanshinone IIA, a lipophilic compound in Salvia miltiorrhiza. This study aimed to investigate the effect of STS on ion transport in mouse tracheal epithelium and the mechanisms underlying it. Short-circuit current (I(sc)) was measured to evaluate the effect of STS on transepithelial ion transport. Intracellular Ca(2+) imaging was performed to observe intracellular Ca(2+) concentration ([Ca(2+)](i)) changes induced by STS in primary cultured mouse tracheal epithelial cells. Results showed that the apical application of STS at mouse trachea elicited an increase of I(sc), which was abrogated by atropine, an antagonist of muscarinic acetylcholine receptor (mAChR). By removing ambient Cl(−) or applying blockers of Ca(2+)-activated Cl(−) channel (CaCC), the response of STS-induced I(sc) was suppressed. Moreover, STS elevated the [Ca(2+)](i) in mouse tracheal epithelial cells. As a result, STS stimulated Cl(−) secretion in mouse tracheal epithelium via CaCC in an mAChR-dependent way. Due to the critical role of Cl(−) secretion in airway hydration, our findings suggested that STS may be used to ameliorate the airway dehydration symptom in cystic fibrosis (CF) and chronic obstructive pulmonary disease (COPD). |
format | Online Article Text |
id | pubmed-5440052 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-54400522017-06-06 Sodium tanshinone IIA sulfonate stimulated Cl(−) secretion in mouse trachea Chen, Peng-Xiao Zhang, Yi-Lin Xu, Jia-Wen Yu, Ming-Hao Huang, Jie-Hong Zhao, Lei Zhou, Wen-Liang PLoS One Research Article Sodium tanshinone IIA sulfonate (STS) is a derivate of tanshinone IIA, a lipophilic compound in Salvia miltiorrhiza. This study aimed to investigate the effect of STS on ion transport in mouse tracheal epithelium and the mechanisms underlying it. Short-circuit current (I(sc)) was measured to evaluate the effect of STS on transepithelial ion transport. Intracellular Ca(2+) imaging was performed to observe intracellular Ca(2+) concentration ([Ca(2+)](i)) changes induced by STS in primary cultured mouse tracheal epithelial cells. Results showed that the apical application of STS at mouse trachea elicited an increase of I(sc), which was abrogated by atropine, an antagonist of muscarinic acetylcholine receptor (mAChR). By removing ambient Cl(−) or applying blockers of Ca(2+)-activated Cl(−) channel (CaCC), the response of STS-induced I(sc) was suppressed. Moreover, STS elevated the [Ca(2+)](i) in mouse tracheal epithelial cells. As a result, STS stimulated Cl(−) secretion in mouse tracheal epithelium via CaCC in an mAChR-dependent way. Due to the critical role of Cl(−) secretion in airway hydration, our findings suggested that STS may be used to ameliorate the airway dehydration symptom in cystic fibrosis (CF) and chronic obstructive pulmonary disease (COPD). Public Library of Science 2017-05-22 /pmc/articles/PMC5440052/ /pubmed/28542554 http://dx.doi.org/10.1371/journal.pone.0178226 Text en © 2017 Chen et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Chen, Peng-Xiao Zhang, Yi-Lin Xu, Jia-Wen Yu, Ming-Hao Huang, Jie-Hong Zhao, Lei Zhou, Wen-Liang Sodium tanshinone IIA sulfonate stimulated Cl(−) secretion in mouse trachea |
title | Sodium tanshinone IIA sulfonate stimulated Cl(−) secretion in mouse trachea |
title_full | Sodium tanshinone IIA sulfonate stimulated Cl(−) secretion in mouse trachea |
title_fullStr | Sodium tanshinone IIA sulfonate stimulated Cl(−) secretion in mouse trachea |
title_full_unstemmed | Sodium tanshinone IIA sulfonate stimulated Cl(−) secretion in mouse trachea |
title_short | Sodium tanshinone IIA sulfonate stimulated Cl(−) secretion in mouse trachea |
title_sort | sodium tanshinone iia sulfonate stimulated cl(−) secretion in mouse trachea |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5440052/ https://www.ncbi.nlm.nih.gov/pubmed/28542554 http://dx.doi.org/10.1371/journal.pone.0178226 |
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