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Anti-malarial activity of traditional Kampo medicine Coptis rhizome extract and its major active compounds

BACKGROUND: Herbal medicine has been a rich source of new drugs exemplified by quinine and artemisinin. In this study, a variety of Japanese traditional herbal medicine (‘Kampo’) were examined for their potential anti-malarial activities. METHODS: A comprehensive screening methods were designed to i...

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Autores principales: Teklemichael, Awet Alem, Mizukami, Shusaku, Toume, Kazufumi, Mosaddeque, Farhana, Kamel, Mohamed Gomaa, Kaneko, Osamu, Komatsu, Katsuko, Karbwang, Juntra, Huy, Nguyen Tien, Hirayama, Kenji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7282140/
https://www.ncbi.nlm.nih.gov/pubmed/32513250
http://dx.doi.org/10.1186/s12936-020-03273-x
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author Teklemichael, Awet Alem
Mizukami, Shusaku
Toume, Kazufumi
Mosaddeque, Farhana
Kamel, Mohamed Gomaa
Kaneko, Osamu
Komatsu, Katsuko
Karbwang, Juntra
Huy, Nguyen Tien
Hirayama, Kenji
author_facet Teklemichael, Awet Alem
Mizukami, Shusaku
Toume, Kazufumi
Mosaddeque, Farhana
Kamel, Mohamed Gomaa
Kaneko, Osamu
Komatsu, Katsuko
Karbwang, Juntra
Huy, Nguyen Tien
Hirayama, Kenji
author_sort Teklemichael, Awet Alem
collection PubMed
description BACKGROUND: Herbal medicine has been a rich source of new drugs exemplified by quinine and artemisinin. In this study, a variety of Japanese traditional herbal medicine (‘Kampo’) were examined for their potential anti-malarial activities. METHODS: A comprehensive screening methods were designed to identify novel anti-malarial drugs from a library of Kampo herbal extracts (n = 120) and related compounds (n = 96). The anti-malarial activity was initially evaluated in vitro against chloroquine/mefloquine-sensitive (3D7) and-resistant (Dd2) strains of Plasmodium falciparum. The cytotoxicity was also evaluated using primary adult mouse brain cells. After being selected through the first in vitro assay, positive extracts and compounds were examined for possible in vivo anti-malarial activity. RESULTS: Out of 120 herbal extracts, Coptis rhizome showed the highest anti-malarial activity (IC(50) 1.9 µg/mL of 3D7 and 4.85 µg/mL of Dd2) with a high selectivity index (SI) > 263 (3D7) and > 103 (Dd2). Three major chlorinated compounds (coptisine, berberine, and palmatine) related to Coptis rhizome also showed anti-malarial activities with IC(50) 1.1, 2.6, and 6.0 µM (against 3D7) and 3.1, 6.3, and 11.8 µM (against Dd2), respectively. Among them, coptisine chloride exhibited the highest anti-malarial activity (IC(50) 1.1 µM against 3D7 and 3.1 µM against Dd2) with SI of 37.8 and 13.2, respectively. Finally, the herbal extract of Coptis rhizome and its major active compound coptisine chloride exhibited significant anti-malarial activity in mice infected with Plasmodium yoelii 17X strain with respect to its activity on parasite suppression consistently from day 3 to day 7 post-challenge. The effect ranged from 50.38 to 72.13% (P < 0.05) for Coptis rhizome and from 81 to 89% (P < 0.01) for coptisine chloride. CONCLUSION: Coptis rhizome and its major active compound coptisine chloride showed promising anti-malarial activity against chloroquine-sensitive (3D7) and -resistant (Dd2) strains in vitro as well as in vivo mouse malaria model. Thus, Kampo herbal medicine is a potential natural resource for novel anti-malarial agents.
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spelling pubmed-72821402020-06-10 Anti-malarial activity of traditional Kampo medicine Coptis rhizome extract and its major active compounds Teklemichael, Awet Alem Mizukami, Shusaku Toume, Kazufumi Mosaddeque, Farhana Kamel, Mohamed Gomaa Kaneko, Osamu Komatsu, Katsuko Karbwang, Juntra Huy, Nguyen Tien Hirayama, Kenji Malar J Research BACKGROUND: Herbal medicine has been a rich source of new drugs exemplified by quinine and artemisinin. In this study, a variety of Japanese traditional herbal medicine (‘Kampo’) were examined for their potential anti-malarial activities. METHODS: A comprehensive screening methods were designed to identify novel anti-malarial drugs from a library of Kampo herbal extracts (n = 120) and related compounds (n = 96). The anti-malarial activity was initially evaluated in vitro against chloroquine/mefloquine-sensitive (3D7) and-resistant (Dd2) strains of Plasmodium falciparum. The cytotoxicity was also evaluated using primary adult mouse brain cells. After being selected through the first in vitro assay, positive extracts and compounds were examined for possible in vivo anti-malarial activity. RESULTS: Out of 120 herbal extracts, Coptis rhizome showed the highest anti-malarial activity (IC(50) 1.9 µg/mL of 3D7 and 4.85 µg/mL of Dd2) with a high selectivity index (SI) > 263 (3D7) and > 103 (Dd2). Three major chlorinated compounds (coptisine, berberine, and palmatine) related to Coptis rhizome also showed anti-malarial activities with IC(50) 1.1, 2.6, and 6.0 µM (against 3D7) and 3.1, 6.3, and 11.8 µM (against Dd2), respectively. Among them, coptisine chloride exhibited the highest anti-malarial activity (IC(50) 1.1 µM against 3D7 and 3.1 µM against Dd2) with SI of 37.8 and 13.2, respectively. Finally, the herbal extract of Coptis rhizome and its major active compound coptisine chloride exhibited significant anti-malarial activity in mice infected with Plasmodium yoelii 17X strain with respect to its activity on parasite suppression consistently from day 3 to day 7 post-challenge. The effect ranged from 50.38 to 72.13% (P < 0.05) for Coptis rhizome and from 81 to 89% (P < 0.01) for coptisine chloride. CONCLUSION: Coptis rhizome and its major active compound coptisine chloride showed promising anti-malarial activity against chloroquine-sensitive (3D7) and -resistant (Dd2) strains in vitro as well as in vivo mouse malaria model. Thus, Kampo herbal medicine is a potential natural resource for novel anti-malarial agents. BioMed Central 2020-06-08 /pmc/articles/PMC7282140/ /pubmed/32513250 http://dx.doi.org/10.1186/s12936-020-03273-x Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Teklemichael, Awet Alem
Mizukami, Shusaku
Toume, Kazufumi
Mosaddeque, Farhana
Kamel, Mohamed Gomaa
Kaneko, Osamu
Komatsu, Katsuko
Karbwang, Juntra
Huy, Nguyen Tien
Hirayama, Kenji
Anti-malarial activity of traditional Kampo medicine Coptis rhizome extract and its major active compounds
title Anti-malarial activity of traditional Kampo medicine Coptis rhizome extract and its major active compounds
title_full Anti-malarial activity of traditional Kampo medicine Coptis rhizome extract and its major active compounds
title_fullStr Anti-malarial activity of traditional Kampo medicine Coptis rhizome extract and its major active compounds
title_full_unstemmed Anti-malarial activity of traditional Kampo medicine Coptis rhizome extract and its major active compounds
title_short Anti-malarial activity of traditional Kampo medicine Coptis rhizome extract and its major active compounds
title_sort anti-malarial activity of traditional kampo medicine coptis rhizome extract and its major active compounds
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7282140/
https://www.ncbi.nlm.nih.gov/pubmed/32513250
http://dx.doi.org/10.1186/s12936-020-03273-x
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