Effects of Schisandra chinensis Baillon (Schizandraceae) on lipopolysaccharide induced lung inflammation in mice

Schisandra chinensis Baillon (Sc), an anti-inflammatory herb that has been used in traditional Chinese medicine for thousands of years, is frequently used to treat upper respiratory tract infections. This study was conducted to evaluate the ability of a water extract of Sc to prevent airway inflamma...

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Veröffentlicht in:Journal of ethnopharmacology 2012-06, Vol.142 (1), p.41-47
Hauptverfasser: Bae, Hyunsu, Kim, Ranah, Kim, Youngeun, Lee, Euijeong, Jin Kim, Hye, Pyo Jang, Young, Jung, Sung-Ki, Kim, Jinju
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container_end_page 47
container_issue 1
container_start_page 41
container_title Journal of ethnopharmacology
container_volume 142
creator Bae, Hyunsu
Kim, Ranah
Kim, Youngeun
Lee, Euijeong
Jin Kim, Hye
Pyo Jang, Young
Jung, Sung-Ki
Kim, Jinju
description Schisandra chinensis Baillon (Sc), an anti-inflammatory herb that has been used in traditional Chinese medicine for thousands of years, is frequently used to treat upper respiratory tract infections. This study was conducted to evaluate the ability of a water extract of Sc to prevent airway inflammation both in vitro and in vivo. Human lung alveolar epithelial-derived A549 cells were stimulated with to interleukin-1β, tumor necrosis factor-α, and interferon-γ (IL-1β, TNF-α, and INF-γ; cytokine mixture; CM) and treated with Sc extracts. They were then evaluated using nitric oxide (NO), IL-8 and monocyte chemotactic protein-1 (MCP-1) secretions. In the in vivo study, BALB/c mice were challenged with lipopolysaccharide (LPS) to induce acute airway inflammation. After this challenge, the mice were treated with Sc extracts (10, 50 and 100mg/kg) by oral administration, and inflammatory cells in the bronchoalveolar lavage (BAL) fluid were counted. IL-6 and TNF-α secretions were measured using an enzyme-linked immunosorbent assay. Lung tissues of the LPS treated mice were prepared and stained with hematoxylin and eosin (HE) for histological examination. In the A549 cells, Sc extracts dose-dependently and significantly inhibited CM-induced NO production and reduced IL-8 and MCP-1 secretions. Sc extracts efficiently suppressed neutrophil and macrophage infiltrations of lung tissues and increased IL-6 and TNF-α levels in BAL fluid in LPS-instilled BALB/c mice. In addition, Sc extracts treatment inhibited pathologic progress in the lung tissues, as confirmed by H&E staining. These findings indicate that Sc extracts could be potentially useful for the treatment of acute lung inflammation and acute lung injury. [Display omitted]
doi_str_mv 10.1016/j.jep.2012.04.009
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This study was conducted to evaluate the ability of a water extract of Sc to prevent airway inflammation both in vitro and in vivo. Human lung alveolar epithelial-derived A549 cells were stimulated with to interleukin-1β, tumor necrosis factor-α, and interferon-γ (IL-1β, TNF-α, and INF-γ; cytokine mixture; CM) and treated with Sc extracts. They were then evaluated using nitric oxide (NO), IL-8 and monocyte chemotactic protein-1 (MCP-1) secretions. In the in vivo study, BALB/c mice were challenged with lipopolysaccharide (LPS) to induce acute airway inflammation. After this challenge, the mice were treated with Sc extracts (10, 50 and 100mg/kg) by oral administration, and inflammatory cells in the bronchoalveolar lavage (BAL) fluid were counted. IL-6 and TNF-α secretions were measured using an enzyme-linked immunosorbent assay. Lung tissues of the LPS treated mice were prepared and stained with hematoxylin and eosin (HE) for histological examination. In the A549 cells, Sc extracts dose-dependently and significantly inhibited CM-induced NO production and reduced IL-8 and MCP-1 secretions. Sc extracts efficiently suppressed neutrophil and macrophage infiltrations of lung tissues and increased IL-6 and TNF-α levels in BAL fluid in LPS-instilled BALB/c mice. In addition, Sc extracts treatment inhibited pathologic progress in the lung tissues, as confirmed by H&amp;E staining. These findings indicate that Sc extracts could be potentially useful for the treatment of acute lung inflammation and acute lung injury. 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This study was conducted to evaluate the ability of a water extract of Sc to prevent airway inflammation both in vitro and in vivo. Human lung alveolar epithelial-derived A549 cells were stimulated with to interleukin-1β, tumor necrosis factor-α, and interferon-γ (IL-1β, TNF-α, and INF-γ; cytokine mixture; CM) and treated with Sc extracts. They were then evaluated using nitric oxide (NO), IL-8 and monocyte chemotactic protein-1 (MCP-1) secretions. In the in vivo study, BALB/c mice were challenged with lipopolysaccharide (LPS) to induce acute airway inflammation. After this challenge, the mice were treated with Sc extracts (10, 50 and 100mg/kg) by oral administration, and inflammatory cells in the bronchoalveolar lavage (BAL) fluid were counted. IL-6 and TNF-α secretions were measured using an enzyme-linked immunosorbent assay. Lung tissues of the LPS treated mice were prepared and stained with hematoxylin and eosin (HE) for histological examination. In the A549 cells, Sc extracts dose-dependently and significantly inhibited CM-induced NO production and reduced IL-8 and MCP-1 secretions. Sc extracts efficiently suppressed neutrophil and macrophage infiltrations of lung tissues and increased IL-6 and TNF-α levels in BAL fluid in LPS-instilled BALB/c mice. In addition, Sc extracts treatment inhibited pathologic progress in the lung tissues, as confirmed by H&amp;E staining. These findings indicate that Sc extracts could be potentially useful for the treatment of acute lung inflammation and acute lung injury. [Display omitted]</description><subject>Acute lung inflammation</subject><subject>Animals</subject><subject>Anti-inflammatory</subject><subject>Anti-Inflammatory Agents - pharmacology</subject><subject>Anti-Inflammatory Agents - therapeutic use</subject><subject>Bronchoalveolar Lavage Fluid - chemistry</subject><subject>Bronchoalveolar Lavage Fluid - cytology</subject><subject>Cell Count</subject><subject>Cell Line, Tumor</subject><subject>Cell Survival - drug effects</subject><subject>Cytokines - metabolism</subject><subject>Drugs, Chinese Herbal - analysis</subject><subject>Drugs, Chinese Herbal - pharmacology</subject><subject>Drugs, Chinese Herbal - therapeutic use</subject><subject>Humans</subject><subject>Lignans - analysis</subject><subject>Lignans - pharmacology</subject><subject>Lignans - therapeutic use</subject><subject>Lipopolysaccharides</subject><subject>Male</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>Nitric Oxide - metabolism</subject><subject>Phytotherapy</subject><subject>Pneumonia - chemically induced</subject><subject>Pneumonia - drug therapy</subject><subject>Pneumonia - metabolism</subject><subject>Pneumonia - pathology</subject><subject>Pulmonary inflammations</subject><subject>Schisandra</subject><subject>Schisandra chinensis Baillon (Schizandraceae)</subject><issn>0378-8741</issn><issn>1872-7573</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kE1v1DAQhi1ERbeFH8AF-VgOSf0ZJ-JEqxaQKnEAztasM6ZeOU6wN0jl19fbLRw5jcfzzCvNQ8hbzlrOeHe5a3e4tIJx0TLVMja8IBveG9EYbeRLsmHS9E1vFD8lZ6XsGGOGK_aKnAqhleRGbshy4z26faGzp9_cfSiQxgy0vhKmEgq9ghDjnOjFYfrnaeoQ8D2tfzEs8zLHhwLO3UMOI9KQxtXhSOOaftbGR5gm2IcKh0Sn4PA1OfEQC755rufkx-3N9-vPzd3XT1-uP941Tmq5byQ67WBEBBi4EM5sheHSdIhMKM0HqY2CAXrBhVfAtdz2jkvtB9312Bsvz8nFMXfJ868Vy95OoTiMERLOa7FV4NBxZURfUX5EXZ5LyejtksME-aFCB66zO1tF24Noy5StouvOu-f4dTvh-G_jr9kKfDgCWI_8HTDb4gKm6ibkKtyOc_hP_COJvY8G</recordid><startdate>20120626</startdate><enddate>20120626</enddate><creator>Bae, Hyunsu</creator><creator>Kim, Ranah</creator><creator>Kim, Youngeun</creator><creator>Lee, Euijeong</creator><creator>Jin Kim, Hye</creator><creator>Pyo Jang, Young</creator><creator>Jung, Sung-Ki</creator><creator>Kim, Jinju</creator><general>Elsevier Ireland Ltd</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>20120626</creationdate><title>Effects of Schisandra chinensis Baillon (Schizandraceae) on lipopolysaccharide induced lung inflammation in mice</title><author>Bae, Hyunsu ; 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This study was conducted to evaluate the ability of a water extract of Sc to prevent airway inflammation both in vitro and in vivo. Human lung alveolar epithelial-derived A549 cells were stimulated with to interleukin-1β, tumor necrosis factor-α, and interferon-γ (IL-1β, TNF-α, and INF-γ; cytokine mixture; CM) and treated with Sc extracts. They were then evaluated using nitric oxide (NO), IL-8 and monocyte chemotactic protein-1 (MCP-1) secretions. In the in vivo study, BALB/c mice were challenged with lipopolysaccharide (LPS) to induce acute airway inflammation. After this challenge, the mice were treated with Sc extracts (10, 50 and 100mg/kg) by oral administration, and inflammatory cells in the bronchoalveolar lavage (BAL) fluid were counted. IL-6 and TNF-α secretions were measured using an enzyme-linked immunosorbent assay. Lung tissues of the LPS treated mice were prepared and stained with hematoxylin and eosin (HE) for histological examination. 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subjects Acute lung inflammation
Animals
Anti-inflammatory
Anti-Inflammatory Agents - pharmacology
Anti-Inflammatory Agents - therapeutic use
Bronchoalveolar Lavage Fluid - chemistry
Bronchoalveolar Lavage Fluid - cytology
Cell Count
Cell Line, Tumor
Cell Survival - drug effects
Cytokines - metabolism
Drugs, Chinese Herbal - analysis
Drugs, Chinese Herbal - pharmacology
Drugs, Chinese Herbal - therapeutic use
Humans
Lignans - analysis
Lignans - pharmacology
Lignans - therapeutic use
Lipopolysaccharides
Male
Mice
Mice, Inbred BALB C
Nitric Oxide - metabolism
Phytotherapy
Pneumonia - chemically induced
Pneumonia - drug therapy
Pneumonia - metabolism
Pneumonia - pathology
Pulmonary inflammations
Schisandra
Schisandra chinensis Baillon (Schizandraceae)
title Effects of Schisandra chinensis Baillon (Schizandraceae) on lipopolysaccharide induced lung inflammation in mice
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