Antitussive, expectorant, and anti-inflammatory effects of Adenophorae Radix powder in ICR mice

Adenophora triphylla var. japonica is frequently used as an oriental medicinal plant in Korea, China, and Japan for its anti-inflammatory, antitussive, and hepatoprotective effects. In the present study, the antitussive, expectorant, and anti-inflammatory effects of AR powder were investigated using...

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Veröffentlicht in:Journal of ethnopharmacology 2019-07, Vol.239, p.111915-111915, Article 111915
Hauptverfasser: Hu, Jin-Ryul, Jung, Chul-Jong, Ku, Seong-Min, Jung, Dae-Hwa, Ku, Sae-Kwang, Choi, Jae-Suk
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container_title Journal of ethnopharmacology
container_volume 239
creator Hu, Jin-Ryul
Jung, Chul-Jong
Ku, Seong-Min
Jung, Dae-Hwa
Ku, Sae-Kwang
Choi, Jae-Suk
description Adenophora triphylla var. japonica is frequently used as an oriental medicinal plant in Korea, China, and Japan for its anti-inflammatory, antitussive, and hepatoprotective effects. In the present study, the antitussive, expectorant, and anti-inflammatory effects of AR powder were investigated using animal models to evaluate their potential to treat respiratory disorders. AR powder was administered orally to mice once daily for 11 days, at dose levels of 400, 200, and 100 mg/kg. Theobromine (TB), ambroxol (AM) and dexamethasone (DEXA) were used as standard drugs for antitussive effects, expectorant effects and anti-inflammatory effects, respectively. Evaluations of antitussive effects were based on changes in body weight, the number of cough responses and the histopathology of the lung and trachea. Expectorant effects were based on changes in the body weight, macroscopic observations of body surface redness, the mucous secretion of the trachea and histopathology of lung (secondary bronchus). Anti-inflammatory effects were based on changes in the body weight, macroscopic observations involving redness and edema of the treated ear, absolute and relative ear weights and histopathology of the treated ears. Allergic acute inflammation and coughing induced by exposure to NH4OH and symptoms of xylene-induced contact dermatitis were significantly inhibited by treatment with AR powder in a dose-dependent manner. Histological analyses revealed that AR powder decreased the OD values in trachea lavage fluid, reduced body surface redness, thicknesses of intrapulmonary secondary bronchus mucosa, and the number of PAS-positive mucous producing cells. Overall, AR powder administered at 200 mg/kg displayed superior antitussive and expectorant effects as compared to TB (50 mg/kg), and AM (250 mg/kg). At the highest concentration (400 mg/kg) AR powder displayed only moderately improved anti-inflammatory activities as compared to DEXA (1 mg/kg). The results obtained in this study suggest that AR powder exerts dose-dependent, favorable antitussive, expectorant, and anti-inflammatory activities achieved through modulation of the activity of mast cells and respiratory mucous production. Therefore, AR powder may serve as a therapeutic agent in various respiratory disorders, especially those that occur as a result of environmental toxicants. [Display omitted]
doi_str_mv 10.1016/j.jep.2019.111915
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In the present study, the antitussive, expectorant, and anti-inflammatory effects of AR powder were investigated using animal models to evaluate their potential to treat respiratory disorders. AR powder was administered orally to mice once daily for 11 days, at dose levels of 400, 200, and 100 mg/kg. Theobromine (TB), ambroxol (AM) and dexamethasone (DEXA) were used as standard drugs for antitussive effects, expectorant effects and anti-inflammatory effects, respectively. Evaluations of antitussive effects were based on changes in body weight, the number of cough responses and the histopathology of the lung and trachea. Expectorant effects were based on changes in the body weight, macroscopic observations of body surface redness, the mucous secretion of the trachea and histopathology of lung (secondary bronchus). Anti-inflammatory effects were based on changes in the body weight, macroscopic observations involving redness and edema of the treated ear, absolute and relative ear weights and histopathology of the treated ears. Allergic acute inflammation and coughing induced by exposure to NH4OH and symptoms of xylene-induced contact dermatitis were significantly inhibited by treatment with AR powder in a dose-dependent manner. Histological analyses revealed that AR powder decreased the OD values in trachea lavage fluid, reduced body surface redness, thicknesses of intrapulmonary secondary bronchus mucosa, and the number of PAS-positive mucous producing cells. Overall, AR powder administered at 200 mg/kg displayed superior antitussive and expectorant effects as compared to TB (50 mg/kg), and AM (250 mg/kg). At the highest concentration (400 mg/kg) AR powder displayed only moderately improved anti-inflammatory activities as compared to DEXA (1 mg/kg). The results obtained in this study suggest that AR powder exerts dose-dependent, favorable antitussive, expectorant, and anti-inflammatory activities achieved through modulation of the activity of mast cells and respiratory mucous production. Therefore, AR powder may serve as a therapeutic agent in various respiratory disorders, especially those that occur as a result of environmental toxicants. 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In the present study, the antitussive, expectorant, and anti-inflammatory effects of AR powder were investigated using animal models to evaluate their potential to treat respiratory disorders. AR powder was administered orally to mice once daily for 11 days, at dose levels of 400, 200, and 100 mg/kg. Theobromine (TB), ambroxol (AM) and dexamethasone (DEXA) were used as standard drugs for antitussive effects, expectorant effects and anti-inflammatory effects, respectively. Evaluations of antitussive effects were based on changes in body weight, the number of cough responses and the histopathology of the lung and trachea. Expectorant effects were based on changes in the body weight, macroscopic observations of body surface redness, the mucous secretion of the trachea and histopathology of lung (secondary bronchus). Anti-inflammatory effects were based on changes in the body weight, macroscopic observations involving redness and edema of the treated ear, absolute and relative ear weights and histopathology of the treated ears. Allergic acute inflammation and coughing induced by exposure to NH4OH and symptoms of xylene-induced contact dermatitis were significantly inhibited by treatment with AR powder in a dose-dependent manner. Histological analyses revealed that AR powder decreased the OD values in trachea lavage fluid, reduced body surface redness, thicknesses of intrapulmonary secondary bronchus mucosa, and the number of PAS-positive mucous producing cells. Overall, AR powder administered at 200 mg/kg displayed superior antitussive and expectorant effects as compared to TB (50 mg/kg), and AM (250 mg/kg). At the highest concentration (400 mg/kg) AR powder displayed only moderately improved anti-inflammatory activities as compared to DEXA (1 mg/kg). The results obtained in this study suggest that AR powder exerts dose-dependent, favorable antitussive, expectorant, and anti-inflammatory activities achieved through modulation of the activity of mast cells and respiratory mucous production. Therefore, AR powder may serve as a therapeutic agent in various respiratory disorders, especially those that occur as a result of environmental toxicants. [Display omitted]</description><subject>Adenophorae radix powder</subject><subject>Ammonium Hydroxide</subject><subject>Animals</subject><subject>Anti-Inflammatory Agents - therapeutic use</subject><subject>Anti-inflammatory effects</subject><subject>Antitussive</subject><subject>Antitussive Agents - therapeutic use</subject><subject>Campanulaceae</subject><subject>Cough - chemically induced</subject><subject>Cough - drug therapy</subject><subject>Cough - metabolism</subject><subject>Cough - pathology</subject><subject>Dermatitis, Contact - drug therapy</subject><subject>Dermatitis, Contact - pathology</subject><subject>Expectorant</subject><subject>Expectorants - therapeutic use</subject><subject>Lung - drug effects</subject><subject>Lung - pathology</subject><subject>Male</subject><subject>Mast cells</subject><subject>Mice, Inbred ICR</subject><subject>Mouse</subject><subject>Mucus - drug effects</subject><subject>Mucus - metabolism</subject><subject>Periodic acid schiff</subject><subject>Plant Roots</subject><subject>Powders</subject><subject>Respiratory Mucosa - drug effects</subject><subject>Respiratory Mucosa - metabolism</subject><subject>Skin - drug effects</subject><subject>Skin - pathology</subject><subject>Trachea - drug effects</subject><subject>Trachea - pathology</subject><subject>Xylenes</subject><issn>0378-8741</issn><issn>1872-7573</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kEtLAzEQx4MoWh8fwIvk6MGtmc2m2cVTKT4KBaHoOWQ3E8zSfZhsfXx7U7Z69DAMzPzmD_Mj5BLYFBjMbutpjf00ZVBMAaAAcUAmkMs0kULyQzJhXOZJLjM4Iach1IwxCRk7JiccGC-yNJ8QNW8HN2xDcB94Q_Grx2rovG6HG6pbE2twiWvtRjeNjotvitZGJNDO0rnBtuvfIo50rY37on33adBT19LlYk0bV-E5ObJ6E_Bi38_I68P9y-IpWT0_LhfzVVJxwYdE2pnIeKG1sUZDCaXgM86FzDMDIgVRCCGsKEouQcah0IYbTBlaU2QaZyU_I9djbu-79y2GQTUuVLjZ6Ba7bVBpCjlnMZJFFEa08l0IHq3qvWu0_1bA1M6rqlX0qnZe1eg13lzt47dlg-bv4ldkBO5GAOOTHw69CpXDtkLjfPSlTOf-if8BMomH-Q</recordid><startdate>20190715</startdate><enddate>20190715</enddate><creator>Hu, Jin-Ryul</creator><creator>Jung, Chul-Jong</creator><creator>Ku, Seong-Min</creator><creator>Jung, Dae-Hwa</creator><creator>Ku, Sae-Kwang</creator><creator>Choi, Jae-Suk</creator><general>Elsevier B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20190715</creationdate><title>Antitussive, expectorant, and anti-inflammatory effects of Adenophorae Radix powder in ICR mice</title><author>Hu, Jin-Ryul ; 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In the present study, the antitussive, expectorant, and anti-inflammatory effects of AR powder were investigated using animal models to evaluate their potential to treat respiratory disorders. AR powder was administered orally to mice once daily for 11 days, at dose levels of 400, 200, and 100 mg/kg. Theobromine (TB), ambroxol (AM) and dexamethasone (DEXA) were used as standard drugs for antitussive effects, expectorant effects and anti-inflammatory effects, respectively. Evaluations of antitussive effects were based on changes in body weight, the number of cough responses and the histopathology of the lung and trachea. Expectorant effects were based on changes in the body weight, macroscopic observations of body surface redness, the mucous secretion of the trachea and histopathology of lung (secondary bronchus). Anti-inflammatory effects were based on changes in the body weight, macroscopic observations involving redness and edema of the treated ear, absolute and relative ear weights and histopathology of the treated ears. Allergic acute inflammation and coughing induced by exposure to NH4OH and symptoms of xylene-induced contact dermatitis were significantly inhibited by treatment with AR powder in a dose-dependent manner. Histological analyses revealed that AR powder decreased the OD values in trachea lavage fluid, reduced body surface redness, thicknesses of intrapulmonary secondary bronchus mucosa, and the number of PAS-positive mucous producing cells. Overall, AR powder administered at 200 mg/kg displayed superior antitussive and expectorant effects as compared to TB (50 mg/kg), and AM (250 mg/kg). At the highest concentration (400 mg/kg) AR powder displayed only moderately improved anti-inflammatory activities as compared to DEXA (1 mg/kg). The results obtained in this study suggest that AR powder exerts dose-dependent, favorable antitussive, expectorant, and anti-inflammatory activities achieved through modulation of the activity of mast cells and respiratory mucous production. Therefore, AR powder may serve as a therapeutic agent in various respiratory disorders, especially those that occur as a result of environmental toxicants. [Display omitted]</abstract><cop>Ireland</cop><pub>Elsevier B.V</pub><pmid>31039428</pmid><doi>10.1016/j.jep.2019.111915</doi><tpages>1</tpages></addata></record>
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subjects Adenophorae radix powder
Ammonium Hydroxide
Animals
Anti-Inflammatory Agents - therapeutic use
Anti-inflammatory effects
Antitussive
Antitussive Agents - therapeutic use
Campanulaceae
Cough - chemically induced
Cough - drug therapy
Cough - metabolism
Cough - pathology
Dermatitis, Contact - drug therapy
Dermatitis, Contact - pathology
Expectorant
Expectorants - therapeutic use
Lung - drug effects
Lung - pathology
Male
Mast cells
Mice, Inbred ICR
Mouse
Mucus - drug effects
Mucus - metabolism
Periodic acid schiff
Plant Roots
Powders
Respiratory Mucosa - drug effects
Respiratory Mucosa - metabolism
Skin - drug effects
Skin - pathology
Trachea - drug effects
Trachea - pathology
Xylenes
title Antitussive, expectorant, and anti-inflammatory effects of Adenophorae Radix powder in ICR mice
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