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Sodium Tanshinone II-A Sulfonate (DS-201) Induces Vasorelaxation of Rat Mesenteric Arteries via Inhibition of L-Type Ca(2+) Channel
Background: We previously have proved that sodium tanshinone II-A sulfonate (DS-201), a derivative of traditional Chinese medicinal herb Danshen (Salvia miltiorrhiza), is an opener and vasodilator of BK(Ca) channel in the vascular smooth muscle cells (VSMCs). Vascular tension is closely associated w...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5801295/ https://www.ncbi.nlm.nih.gov/pubmed/29456510 http://dx.doi.org/10.3389/fphar.2018.00062 |
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author | Zhang, Xiao-Dong He, Chun-Xia Cheng, Jun Wen, Jing Li, Peng-Yun Wang, Na Li, Guang Zeng, Xiao-Rong Cao, Ji-Min Yang, Yan |
author_facet | Zhang, Xiao-Dong He, Chun-Xia Cheng, Jun Wen, Jing Li, Peng-Yun Wang, Na Li, Guang Zeng, Xiao-Rong Cao, Ji-Min Yang, Yan |
author_sort | Zhang, Xiao-Dong |
collection | PubMed |
description | Background: We previously have proved that sodium tanshinone II-A sulfonate (DS-201), a derivative of traditional Chinese medicinal herb Danshen (Salvia miltiorrhiza), is an opener and vasodilator of BK(Ca) channel in the vascular smooth muscle cells (VSMCs). Vascular tension is closely associated with Ca(2+) dynamics and activation of BK(Ca) channel may not be the sole mechanism for the relaxation of the vascular tension by DS-201. Therefore, we hypothesized that the vasorelaxing effect of DS-20 may be also related to Ca(2+) channel and cytoplasmic Ca(2+) level in the VSMCs. Methods: Arterial tension was measured by Danish Myo Technology (DMT) myograph system in the mesentery vessels of rats, intracellular Ca(2+) level by fluorescence imaging system in the VSMCs of rats, and L-type Ca(2+) current by patch clamp technique in Ca(2+) channels transfected human embryonic kidney 293 (HEK-293) cells. Results: DS-201 relaxed the endothelium-denuded artery rings pre-constricted with PE or high K(+) and the vasorelaxation was reversible. Blockade of K(+) channel did not totally block the effect of DS-201 on vasorelaxation. DS-201 suppressed [Ca(2+)](i) transient induced by high K(+) in a concentration-dependent manner in the VSMCs, including the amplitude of Ca(2+) transient, the time for Ca(2+) transient reaching to the [Ca(2+)](i) peak and the time to remove Ca(2+) from the cytoplasm. DS-201 inhibited L-type Ca(2+) channel with an EC(50) of 59.5 μM and at about 40% efficacy of inhibition. However, DS-201did not significantly affect the kinetics of Ca(2+) channel. The effect of DS-201 on L-type Ca(2+) channel was rate-independent. Conclusion: The effect of DS-201 on vasorelaxation was not only via activating BK(Ca) channel, but also blocking Ca(2+) channel and inhibiting Ca(2+) influx in the VSMCs of rats. The results favor the use of DS-201 and Danshen in the treatment of cardiovascular diseases clinically. |
format | Online Article Text |
id | pubmed-5801295 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-58012952018-02-16 Sodium Tanshinone II-A Sulfonate (DS-201) Induces Vasorelaxation of Rat Mesenteric Arteries via Inhibition of L-Type Ca(2+) Channel Zhang, Xiao-Dong He, Chun-Xia Cheng, Jun Wen, Jing Li, Peng-Yun Wang, Na Li, Guang Zeng, Xiao-Rong Cao, Ji-Min Yang, Yan Front Pharmacol Pharmacology Background: We previously have proved that sodium tanshinone II-A sulfonate (DS-201), a derivative of traditional Chinese medicinal herb Danshen (Salvia miltiorrhiza), is an opener and vasodilator of BK(Ca) channel in the vascular smooth muscle cells (VSMCs). Vascular tension is closely associated with Ca(2+) dynamics and activation of BK(Ca) channel may not be the sole mechanism for the relaxation of the vascular tension by DS-201. Therefore, we hypothesized that the vasorelaxing effect of DS-20 may be also related to Ca(2+) channel and cytoplasmic Ca(2+) level in the VSMCs. Methods: Arterial tension was measured by Danish Myo Technology (DMT) myograph system in the mesentery vessels of rats, intracellular Ca(2+) level by fluorescence imaging system in the VSMCs of rats, and L-type Ca(2+) current by patch clamp technique in Ca(2+) channels transfected human embryonic kidney 293 (HEK-293) cells. Results: DS-201 relaxed the endothelium-denuded artery rings pre-constricted with PE or high K(+) and the vasorelaxation was reversible. Blockade of K(+) channel did not totally block the effect of DS-201 on vasorelaxation. DS-201 suppressed [Ca(2+)](i) transient induced by high K(+) in a concentration-dependent manner in the VSMCs, including the amplitude of Ca(2+) transient, the time for Ca(2+) transient reaching to the [Ca(2+)](i) peak and the time to remove Ca(2+) from the cytoplasm. DS-201 inhibited L-type Ca(2+) channel with an EC(50) of 59.5 μM and at about 40% efficacy of inhibition. However, DS-201did not significantly affect the kinetics of Ca(2+) channel. The effect of DS-201 on L-type Ca(2+) channel was rate-independent. Conclusion: The effect of DS-201 on vasorelaxation was not only via activating BK(Ca) channel, but also blocking Ca(2+) channel and inhibiting Ca(2+) influx in the VSMCs of rats. The results favor the use of DS-201 and Danshen in the treatment of cardiovascular diseases clinically. Frontiers Media S.A. 2018-02-02 /pmc/articles/PMC5801295/ /pubmed/29456510 http://dx.doi.org/10.3389/fphar.2018.00062 Text en Copyright © 2018 Zhang, He, Cheng, Wen, Li, Wang, Li, Zeng, Cao and Yang. 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) and the copyright owner 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 Zhang, Xiao-Dong He, Chun-Xia Cheng, Jun Wen, Jing Li, Peng-Yun Wang, Na Li, Guang Zeng, Xiao-Rong Cao, Ji-Min Yang, Yan Sodium Tanshinone II-A Sulfonate (DS-201) Induces Vasorelaxation of Rat Mesenteric Arteries via Inhibition of L-Type Ca(2+) Channel |
title | Sodium Tanshinone II-A Sulfonate (DS-201) Induces Vasorelaxation of Rat Mesenteric Arteries via Inhibition of L-Type Ca(2+) Channel |
title_full | Sodium Tanshinone II-A Sulfonate (DS-201) Induces Vasorelaxation of Rat Mesenteric Arteries via Inhibition of L-Type Ca(2+) Channel |
title_fullStr | Sodium Tanshinone II-A Sulfonate (DS-201) Induces Vasorelaxation of Rat Mesenteric Arteries via Inhibition of L-Type Ca(2+) Channel |
title_full_unstemmed | Sodium Tanshinone II-A Sulfonate (DS-201) Induces Vasorelaxation of Rat Mesenteric Arteries via Inhibition of L-Type Ca(2+) Channel |
title_short | Sodium Tanshinone II-A Sulfonate (DS-201) Induces Vasorelaxation of Rat Mesenteric Arteries via Inhibition of L-Type Ca(2+) Channel |
title_sort | sodium tanshinone ii-a sulfonate (ds-201) induces vasorelaxation of rat mesenteric arteries via inhibition of l-type ca(2+) channel |
topic | Pharmacology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5801295/ https://www.ncbi.nlm.nih.gov/pubmed/29456510 http://dx.doi.org/10.3389/fphar.2018.00062 |
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