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Effects of Morus alba L. and Natural Products Including Morusin on In Vivo Secretion and In Vitro Production of Airway MUC5AC Mucin

BACKGROUND: It is valuable to find the potential activity of regulating the excessive mucin secretion by the compounds derived from various medicinal plants. We investigated whether aqueous extract of the root bark of Morus alba L. (AMA), kuwanon E, kuwanon G, mulberrofuran G, and morusin significan...

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Autores principales: Lee, Hyun Jae, Ryu, Jiho, Park, Su Hyun, Woo, Eun-Rhan, Kim, A Ryun, Lee, Sang Kook, Kim, Yeong Shik, Kim, Ju-Ock, Hong, Jang-Hee, Lee, Choong Jae
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Academy of Tuberculosis and Respiratory Diseases 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4165662/
https://www.ncbi.nlm.nih.gov/pubmed/25237377
http://dx.doi.org/10.4046/trd.2014.77.2.65
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author Lee, Hyun Jae
Ryu, Jiho
Park, Su Hyun
Woo, Eun-Rhan
Kim, A Ryun
Lee, Sang Kook
Kim, Yeong Shik
Kim, Ju-Ock
Hong, Jang-Hee
Lee, Choong Jae
author_facet Lee, Hyun Jae
Ryu, Jiho
Park, Su Hyun
Woo, Eun-Rhan
Kim, A Ryun
Lee, Sang Kook
Kim, Yeong Shik
Kim, Ju-Ock
Hong, Jang-Hee
Lee, Choong Jae
author_sort Lee, Hyun Jae
collection PubMed
description BACKGROUND: It is valuable to find the potential activity of regulating the excessive mucin secretion by the compounds derived from various medicinal plants. We investigated whether aqueous extract of the root bark of Morus alba L. (AMA), kuwanon E, kuwanon G, mulberrofuran G, and morusin significantly affect the secretion and production of airway mucin using in vivo and in vitro experimental models. METHODS: Effect of AMA was examined on hypersecretion of airway mucin in sulfur dioxide-induced acute bronchitis in rats. Confluent NCI-H292 cells were pretreated with ethanolic extract, kuwanon E, kuwanon G, mulberrofuran G, or morusin for 30 minutes and then stimulated with phorbol 12-myristate 13-acetate (PMA) for 24 hours. The MUC5AC mucin secretion and production were measured by enzyme-linked immunosorbent assay. RESULTS: AMA stimulated the secretion of airway mucin in sulfur dioxide-induced bronchitis rat model; aqueous extract, ethanolic extract, kuwanon E, kuwanon G, mulberrofuran G and morusin inhibited the production of MUC5AC mucin induced by PMA from NCI-H292 cells, respectively. CONCLUSION: These results suggest that extract of the root bark and the natural products derived from Morus alba L. can regulate the secretion and production of airway mucin and, at least in part, explains the folk use of extract of Morus alba L. as mucoregulators in diverse inflammatory pulmonary diseases.
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spelling pubmed-41656622014-09-18 Effects of Morus alba L. and Natural Products Including Morusin on In Vivo Secretion and In Vitro Production of Airway MUC5AC Mucin Lee, Hyun Jae Ryu, Jiho Park, Su Hyun Woo, Eun-Rhan Kim, A Ryun Lee, Sang Kook Kim, Yeong Shik Kim, Ju-Ock Hong, Jang-Hee Lee, Choong Jae Tuberc Respir Dis (Seoul) Original Article BACKGROUND: It is valuable to find the potential activity of regulating the excessive mucin secretion by the compounds derived from various medicinal plants. We investigated whether aqueous extract of the root bark of Morus alba L. (AMA), kuwanon E, kuwanon G, mulberrofuran G, and morusin significantly affect the secretion and production of airway mucin using in vivo and in vitro experimental models. METHODS: Effect of AMA was examined on hypersecretion of airway mucin in sulfur dioxide-induced acute bronchitis in rats. Confluent NCI-H292 cells were pretreated with ethanolic extract, kuwanon E, kuwanon G, mulberrofuran G, or morusin for 30 minutes and then stimulated with phorbol 12-myristate 13-acetate (PMA) for 24 hours. The MUC5AC mucin secretion and production were measured by enzyme-linked immunosorbent assay. RESULTS: AMA stimulated the secretion of airway mucin in sulfur dioxide-induced bronchitis rat model; aqueous extract, ethanolic extract, kuwanon E, kuwanon G, mulberrofuran G and morusin inhibited the production of MUC5AC mucin induced by PMA from NCI-H292 cells, respectively. CONCLUSION: These results suggest that extract of the root bark and the natural products derived from Morus alba L. can regulate the secretion and production of airway mucin and, at least in part, explains the folk use of extract of Morus alba L. as mucoregulators in diverse inflammatory pulmonary diseases. The Korean Academy of Tuberculosis and Respiratory Diseases 2014-08 2014-08-29 /pmc/articles/PMC4165662/ /pubmed/25237377 http://dx.doi.org/10.4046/trd.2014.77.2.65 Text en Copyright©2014. The Korean Academy of Tuberculosis and Respiratory Diseases. All rights reserved. http://creativecommons.org/licenses/by-nc/3.0/ It is identical to the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/)
spellingShingle Original Article
Lee, Hyun Jae
Ryu, Jiho
Park, Su Hyun
Woo, Eun-Rhan
Kim, A Ryun
Lee, Sang Kook
Kim, Yeong Shik
Kim, Ju-Ock
Hong, Jang-Hee
Lee, Choong Jae
Effects of Morus alba L. and Natural Products Including Morusin on In Vivo Secretion and In Vitro Production of Airway MUC5AC Mucin
title Effects of Morus alba L. and Natural Products Including Morusin on In Vivo Secretion and In Vitro Production of Airway MUC5AC Mucin
title_full Effects of Morus alba L. and Natural Products Including Morusin on In Vivo Secretion and In Vitro Production of Airway MUC5AC Mucin
title_fullStr Effects of Morus alba L. and Natural Products Including Morusin on In Vivo Secretion and In Vitro Production of Airway MUC5AC Mucin
title_full_unstemmed Effects of Morus alba L. and Natural Products Including Morusin on In Vivo Secretion and In Vitro Production of Airway MUC5AC Mucin
title_short Effects of Morus alba L. and Natural Products Including Morusin on In Vivo Secretion and In Vitro Production of Airway MUC5AC Mucin
title_sort effects of morus alba l. and natural products including morusin on in vivo secretion and in vitro production of airway muc5ac mucin
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4165662/
https://www.ncbi.nlm.nih.gov/pubmed/25237377
http://dx.doi.org/10.4046/trd.2014.77.2.65
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