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Identification of Alkaloids from Corydalis yanhusuo W. T. Wang as Dopamine D(1) Receptor Antagonists by Using CRE-Luciferase Reporter Gene Assay

Corydalis yanhusuo W. T. Wang (C. yanhusuo) has been traditionally used for drug addiction and pain relief in China. In our previous study, we showed that the extract of C. yanhusuo blocks dopamine receptors, demonstrating that its pharmacological activities are mostly due to the antagonistic effect...

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Detalles Bibliográficos
Autores principales: Wu, Lehao, Zhang, Weiyue, Qiu, Xin, Wang, Chaoran, Liu, Yanfang, Wang, Zhiwei, Yu, Yang, Ye, Richard D., Zhang, Yan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6222624/
https://www.ncbi.nlm.nih.gov/pubmed/30308941
http://dx.doi.org/10.3390/molecules23102585
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author Wu, Lehao
Zhang, Weiyue
Qiu, Xin
Wang, Chaoran
Liu, Yanfang
Wang, Zhiwei
Yu, Yang
Ye, Richard D.
Zhang, Yan
author_facet Wu, Lehao
Zhang, Weiyue
Qiu, Xin
Wang, Chaoran
Liu, Yanfang
Wang, Zhiwei
Yu, Yang
Ye, Richard D.
Zhang, Yan
author_sort Wu, Lehao
collection PubMed
description Corydalis yanhusuo W. T. Wang (C. yanhusuo) has been traditionally used for drug addiction and pain relief in China. In our previous study, we showed that the extract of C. yanhusuo blocks dopamine receptors, demonstrating that its pharmacological activities are mostly due to the antagonistic effects of some of its components at dopamine receptors. As part of our ongoing project on C. yanhusuo, the aim of the present study is to establish a high-throughput and low-cost screening assay system and test the abilities of the isolated alkaloids from C. yanhusuo to inhibit dopamine-induced dopamine D(1) receptor activity. By using our established cyclic adenosine monophosphate (cAMP)-response element (CRE)-luciferase reporter gene assay system, we identified eight alkaloids from C. yanhusuo with D(1) receptor antagonistic activities. We next validated the activities of these compounds using fluorometric imaging plate reader (FLIPR) assay by measuring the intracellular Ca(2+) change. Six out of eight compounds, including tetrahydropalmatine, corydaline, 13-methyldehydrocorydalmine, dehydrocorybubine, dehydrocorydaline, and columbamine, can be confirmed for their inhibitory activities. The dopamine-receptor-antagonistic effects of four compounds, including 13-methyldehydrocorydalmine, dehydrocorydaline, columbamine, and corydaline, are reported for the first time. The present study provides an important pharmacological basis to support the traditional use of C. yanhusuo in China.
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spelling pubmed-62226242018-11-13 Identification of Alkaloids from Corydalis yanhusuo W. T. Wang as Dopamine D(1) Receptor Antagonists by Using CRE-Luciferase Reporter Gene Assay Wu, Lehao Zhang, Weiyue Qiu, Xin Wang, Chaoran Liu, Yanfang Wang, Zhiwei Yu, Yang Ye, Richard D. Zhang, Yan Molecules Article Corydalis yanhusuo W. T. Wang (C. yanhusuo) has been traditionally used for drug addiction and pain relief in China. In our previous study, we showed that the extract of C. yanhusuo blocks dopamine receptors, demonstrating that its pharmacological activities are mostly due to the antagonistic effects of some of its components at dopamine receptors. As part of our ongoing project on C. yanhusuo, the aim of the present study is to establish a high-throughput and low-cost screening assay system and test the abilities of the isolated alkaloids from C. yanhusuo to inhibit dopamine-induced dopamine D(1) receptor activity. By using our established cyclic adenosine monophosphate (cAMP)-response element (CRE)-luciferase reporter gene assay system, we identified eight alkaloids from C. yanhusuo with D(1) receptor antagonistic activities. We next validated the activities of these compounds using fluorometric imaging plate reader (FLIPR) assay by measuring the intracellular Ca(2+) change. Six out of eight compounds, including tetrahydropalmatine, corydaline, 13-methyldehydrocorydalmine, dehydrocorybubine, dehydrocorydaline, and columbamine, can be confirmed for their inhibitory activities. The dopamine-receptor-antagonistic effects of four compounds, including 13-methyldehydrocorydalmine, dehydrocorydaline, columbamine, and corydaline, are reported for the first time. The present study provides an important pharmacological basis to support the traditional use of C. yanhusuo in China. MDPI 2018-10-10 /pmc/articles/PMC6222624/ /pubmed/30308941 http://dx.doi.org/10.3390/molecules23102585 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Wu, Lehao
Zhang, Weiyue
Qiu, Xin
Wang, Chaoran
Liu, Yanfang
Wang, Zhiwei
Yu, Yang
Ye, Richard D.
Zhang, Yan
Identification of Alkaloids from Corydalis yanhusuo W. T. Wang as Dopamine D(1) Receptor Antagonists by Using CRE-Luciferase Reporter Gene Assay
title Identification of Alkaloids from Corydalis yanhusuo W. T. Wang as Dopamine D(1) Receptor Antagonists by Using CRE-Luciferase Reporter Gene Assay
title_full Identification of Alkaloids from Corydalis yanhusuo W. T. Wang as Dopamine D(1) Receptor Antagonists by Using CRE-Luciferase Reporter Gene Assay
title_fullStr Identification of Alkaloids from Corydalis yanhusuo W. T. Wang as Dopamine D(1) Receptor Antagonists by Using CRE-Luciferase Reporter Gene Assay
title_full_unstemmed Identification of Alkaloids from Corydalis yanhusuo W. T. Wang as Dopamine D(1) Receptor Antagonists by Using CRE-Luciferase Reporter Gene Assay
title_short Identification of Alkaloids from Corydalis yanhusuo W. T. Wang as Dopamine D(1) Receptor Antagonists by Using CRE-Luciferase Reporter Gene Assay
title_sort identification of alkaloids from corydalis yanhusuo w. t. wang as dopamine d(1) receptor antagonists by using cre-luciferase reporter gene assay
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6222624/
https://www.ncbi.nlm.nih.gov/pubmed/30308941
http://dx.doi.org/10.3390/molecules23102585
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