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Anti-inflammatory, expectorant, and antitussive properties of Kyeongok-go in ICR mice

CONTEXT: Kyeongok-go (KOG) is a traditional mixed herb preparation consisting of Panax ginseng CA Meyer (Araliaceae), Poria cocos Wolf (Polyporaceae), Rehmannia glutinosa (Gaertner) Liboschitz ex Steudel (Orobanchaceae), and honey. Various pharmacological effects of KOG are reported, but the efficac...

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Autores principales: Hu, Jin-Ryul, Jung, Chul-Jong, Ku, Seong-Min, Jung, Dae-Hwa, Bashir, Khawaja Muhammad Imran, Ku, Sae-Kwang, Choi, Jae-Suk
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8008926/
https://www.ncbi.nlm.nih.gov/pubmed/33770452
http://dx.doi.org/10.1080/13880209.2021.1892155
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author Hu, Jin-Ryul
Jung, Chul-Jong
Ku, Seong-Min
Jung, Dae-Hwa
Bashir, Khawaja Muhammad Imran
Ku, Sae-Kwang
Choi, Jae-Suk
author_facet Hu, Jin-Ryul
Jung, Chul-Jong
Ku, Seong-Min
Jung, Dae-Hwa
Bashir, Khawaja Muhammad Imran
Ku, Sae-Kwang
Choi, Jae-Suk
author_sort Hu, Jin-Ryul
collection PubMed
description CONTEXT: Kyeongok-go (KOG) is a traditional mixed herb preparation consisting of Panax ginseng CA Meyer (Araliaceae), Poria cocos Wolf (Polyporaceae), Rehmannia glutinosa (Gaertner) Liboschitz ex Steudel (Orobanchaceae), and honey. Various pharmacological effects of KOG are reported, but the efficacy on respiratory diseases has not been evaluated. OBJECTIVE: The anti-inflammatory, expectorant, and antitussive properties of KOG were examined using animal models of respiratory diseases. MATERIALS AND METHODS: KOG (100, 200, and 400 mg/kg) was orally administered to ICR mice (n = 8) once a day for 11 days. Anti-inflammatory effects of vehicle, xylene, KOG and DEXA (1 mg/kg) were determined by monitoring edoema and redness of treated ears, and measuring the relative and absolute weight of each ear. Expectorant properties of vehicle, KOG and AM (250 mg/kg) were evaluated by observing body surface redness, and the amount of mucous secreted by the trachea. The antitussive potential of vehicle, NH(4)OH, KOG and TB (50 mg/kg) was evaluated by monitoring changes in the number of coughs (for 6 min). RESULTS: KOG (400 mg/kg) treated mice showed 31.29% and 30.72% (p < 0.01) decreases in the relative and absolute weights of each ear relative to xylene control mice, 39.06% increases (p < 0.01) in TLF OD values relative to intact vehicle control mice, and 59.53% decrease (p < 0.01) in coughing compared to NH(4)OH control mice. Dose-dependent changes were observed in all experimental models. CONCLUSIONS: KOG may be a potential therapeutic agent for the treatment of various respiratory diseases, particularly those caused by environmental toxins.
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spelling pubmed-80089262021-04-06 Anti-inflammatory, expectorant, and antitussive properties of Kyeongok-go in ICR mice Hu, Jin-Ryul Jung, Chul-Jong Ku, Seong-Min Jung, Dae-Hwa Bashir, Khawaja Muhammad Imran Ku, Sae-Kwang Choi, Jae-Suk Pharm Biol Research Article CONTEXT: Kyeongok-go (KOG) is a traditional mixed herb preparation consisting of Panax ginseng CA Meyer (Araliaceae), Poria cocos Wolf (Polyporaceae), Rehmannia glutinosa (Gaertner) Liboschitz ex Steudel (Orobanchaceae), and honey. Various pharmacological effects of KOG are reported, but the efficacy on respiratory diseases has not been evaluated. OBJECTIVE: The anti-inflammatory, expectorant, and antitussive properties of KOG were examined using animal models of respiratory diseases. MATERIALS AND METHODS: KOG (100, 200, and 400 mg/kg) was orally administered to ICR mice (n = 8) once a day for 11 days. Anti-inflammatory effects of vehicle, xylene, KOG and DEXA (1 mg/kg) were determined by monitoring edoema and redness of treated ears, and measuring the relative and absolute weight of each ear. Expectorant properties of vehicle, KOG and AM (250 mg/kg) were evaluated by observing body surface redness, and the amount of mucous secreted by the trachea. The antitussive potential of vehicle, NH(4)OH, KOG and TB (50 mg/kg) was evaluated by monitoring changes in the number of coughs (for 6 min). RESULTS: KOG (400 mg/kg) treated mice showed 31.29% and 30.72% (p < 0.01) decreases in the relative and absolute weights of each ear relative to xylene control mice, 39.06% increases (p < 0.01) in TLF OD values relative to intact vehicle control mice, and 59.53% decrease (p < 0.01) in coughing compared to NH(4)OH control mice. Dose-dependent changes were observed in all experimental models. CONCLUSIONS: KOG may be a potential therapeutic agent for the treatment of various respiratory diseases, particularly those caused by environmental toxins. Taylor & Francis 2021-03-26 /pmc/articles/PMC8008926/ /pubmed/33770452 http://dx.doi.org/10.1080/13880209.2021.1892155 Text en © 2021 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://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/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Hu, Jin-Ryul
Jung, Chul-Jong
Ku, Seong-Min
Jung, Dae-Hwa
Bashir, Khawaja Muhammad Imran
Ku, Sae-Kwang
Choi, Jae-Suk
Anti-inflammatory, expectorant, and antitussive properties of Kyeongok-go in ICR mice
title Anti-inflammatory, expectorant, and antitussive properties of Kyeongok-go in ICR mice
title_full Anti-inflammatory, expectorant, and antitussive properties of Kyeongok-go in ICR mice
title_fullStr Anti-inflammatory, expectorant, and antitussive properties of Kyeongok-go in ICR mice
title_full_unstemmed Anti-inflammatory, expectorant, and antitussive properties of Kyeongok-go in ICR mice
title_short Anti-inflammatory, expectorant, and antitussive properties of Kyeongok-go in ICR mice
title_sort anti-inflammatory, expectorant, and antitussive properties of kyeongok-go in icr mice
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8008926/
https://www.ncbi.nlm.nih.gov/pubmed/33770452
http://dx.doi.org/10.1080/13880209.2021.1892155
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