Antioxidant and antiasthmatic effects of saucerneol D in a mouse model of airway inflammation

Chronic airway inflammation is a hallmark of asthma, which is an immune-based disease. We evaluated the ability of saucerneol D, a tetrahydrofuran-type sesquilignan isolated from Saururus chinensis, to regulate airway inflammation in an ovalbumin (OVA)-induced airway inflammation model. Furthermore,...

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Published inInternational immunopharmacology Vol. 11; no. 6; pp. 698 - 705
Main Authors Jung, Ju-Young, Lee, Kyoung-youl, Lee, Mee-Young, Jung, Dayoung, Cho, Eun-Sang, Son, Hwa-Young
Format Journal Article
LanguageEnglish
Published Kidlington Elsevier B.V 01.06.2011
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Abstract Chronic airway inflammation is a hallmark of asthma, which is an immune-based disease. We evaluated the ability of saucerneol D, a tetrahydrofuran-type sesquilignan isolated from Saururus chinensis, to regulate airway inflammation in an ovalbumin (OVA)-induced airway inflammation model. Furthermore, we determined whether heme oxygenase (HO)-1 was required for the protective activity of saucerneol D. The airways of OVA-sensitized mice exposed to an OVA challenge developed eosinophilia and mucus hypersecretion and exhibited increased cytokine levels. Mice were administered saucerneol D orally at doses of 20 and 40 mg/kg once daily on days 26–30. Saucerneol D administered orally significantly inhibited the number of OVA-induced inflammatory cells and the production of immunoglobulin E as well as Th2-type cytokines. Histopathology studies revealed a marked decrease in lung inflammation and goblet cell hyperplasia after saucerneol D treatment. In addition, saucerneol D induced HO-1 and led to a marked decrease in OVA-induced reactive oxygen species and malondialdehyde and an increase in superoxide dismutase and glutathione in lung tissues. These antioxidant effects were correlated with HO-1 induction. In our experiments, saucerneol D treatment reduced airway inflammation and suppressed oxidative stress in an OVA-induced asthma model.
AbstractList Chronic airway inflammation is a hallmark of asthma, which is an immune-based disease. We evaluated the ability of saucerneol D, a tetrahydrofuran-type sesquilignan isolated from Saururus chinensis, to regulate airway inflammation in an ovalbumin (OVA)-induced airway inflammation model. Furthermore, we determined whether heme oxygenase (HO)-1 was required for the protective activity of saucerneol D. The airways of OVA-sensitized mice exposed to an OVA challenge developed eosinophilia and mucus hypersecretion and exhibited increased cytokine levels. Mice were administered saucerneol D orally at doses of 20 and 40mg/kg once daily on days 26-30. Saucerneol D administered orally significantly inhibited the number of OVA-induced inflammatory cells and the production of immunoglobulin E as well as Th2-type cytokines. Histopathology studies revealed a marked decrease in lung inflammation and goblet cell hyperplasia after saucerneol D treatment. In addition, saucerneol D induced HO-1 and led to a marked decrease in OVA-induced reactive oxygen species and malondialdehyde and an increase in superoxide dismutase and glutathione in lung tissues. These antioxidant effects were correlated with HO-1 induction. In our experiments, saucerneol D treatment reduced airway inflammation and suppressed oxidative stress in an OVA-induced asthma model.
Chronic airway inflammation is a hallmark of asthma, which is an immune-based disease. We evaluated the ability of saucerneol D, a tetrahydrofuran-type sesquilignan isolated from Saururus chinensis, to regulate airway inflammation in an ovalbumin (OVA)-induced airway inflammation model. Furthermore, we determined whether heme oxygenase (HO)-1 was required for the protective activity of saucerneol D. The airways of OVA-sensitized mice exposed to an OVA challenge developed eosinophilia and mucus hypersecretion and exhibited increased cytokine levels. Mice were administered saucerneol D orally at doses of 20 and 40 mg/kg once daily on days 26–30. Saucerneol D administered orally significantly inhibited the number of OVA-induced inflammatory cells and the production of immunoglobulin E as well as Th2-type cytokines. Histopathology studies revealed a marked decrease in lung inflammation and goblet cell hyperplasia after saucerneol D treatment. In addition, saucerneol D induced HO-1 and led to a marked decrease in OVA-induced reactive oxygen species and malondialdehyde and an increase in superoxide dismutase and glutathione in lung tissues. These antioxidant effects were correlated with HO-1 induction. In our experiments, saucerneol D treatment reduced airway inflammation and suppressed oxidative stress in an OVA-induced asthma model.
Chronic airway inflammation is a hallmark of asthma, which is an immune-based disease. We evaluated the ability of saucerneol D, a tetrahydrofuran-type sesquilignan isolated from Saururus chinensis, to regulate airway inflammation in an ovalbumin (OVA)-induced airway inflammation model. Furthermore, we determined whether heme oxygenase (HO)-1 was required for the protective activity of saucerneol D. The airways of OVA-sensitized mice exposed to an OVA challenge developed eosinophilia and mucus hypersecretion and exhibited increased cytokine levels. Mice were administered saucerneol D orally at doses of 20 and 40 mg/kg once daily on days 26-30. Saucerneol D administered orally significantly inhibited the number of OVA-induced inflammatory cells and the production of immunoglobulin E as well as Th2-type cytokines. Histopathology studies revealed a marked decrease in lung inflammation and goblet cell hyperplasia after saucerneol D treatment. In addition, saucerneol D induced HO-1 and led to a marked decrease in OVA-induced reactive oxygen species and malondialdehyde and an increase in superoxide dismutase and glutathione in lung tissues. These antioxidant effects were correlated with HO-1 induction. In our experiments, saucerneol D treatment reduced airway inflammation and suppressed oxidative stress in an OVA-induced asthma model.
Author Son, Hwa-Young
Cho, Eun-Sang
Lee, Mee-Young
Lee, Kyoung-youl
Jung, Dayoung
Jung, Ju-Young
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Issue 6
Keywords Saucerneol D
Eosinophilia
Cytokine
Heme oxygenase-1
Asthma
Lung disease
Animal model
Enzyme
Respiratory disease
Rodentia
Heme oxygenase (decyclizing)
Hemopathy
Inflammation
Antiasthma agent
Antioxidant
Respiratory system
Respiratory tract
Vertebrata
Mammalia
Mouse
Heat shock protein
Bronchus disease
Obstructive pulmonary disease
Oxidoreductases
Language English
License CC BY 4.0
Copyright © 2011 Elsevier B.V. All rights reserved.
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Snippet Chronic airway inflammation is a hallmark of asthma, which is an immune-based disease. We evaluated the ability of saucerneol D, a tetrahydrofuran-type...
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SubjectTerms Animals
Anti-Asthmatic Agents - administration & dosage
Anti-Asthmatic Agents - chemistry
Antioxidants - administration & dosage
Antioxidants - chemistry
Asthma
Asthma - drug therapy
Asthma - immunology
Biological and medical sciences
Cells, Cultured
Chronic obstructive pulmonary disease, asthma
Cytokine
Cytokines - genetics
Cytokines - metabolism
Disease Models, Animal
Eosinophilia
Female
Hematologic and hematopoietic diseases
Heme Oxygenase (Decyclizing) - genetics
Heme Oxygenase (Decyclizing) - metabolism
Heme oxygenase-1
Humans
Immunoglobulin E - biosynthesis
Immunoglobulin E - blood
Immunoglobulin E - genetics
Lignans - administration & dosage
Lignans - chemistry
Lignans - pharmacology
Medical sciences
Mice
Mice, Inbred BALB C
Other diseases. Hematologic involvement in other diseases
Pharmacology. Drug treatments
Pneumology
Pneumonia - chemically induced
Pneumonia - drug therapy
Pneumonia - immunology
Reactive Oxygen Species - metabolism
Saucerneol D
Saururaceae - immunology
Saururus
Th1-Th2 Balance - drug effects
Title Antioxidant and antiasthmatic effects of saucerneol D in a mouse model of airway inflammation
URI https://dx.doi.org/10.1016/j.intimp.2011.01.015
https://www.ncbi.nlm.nih.gov/pubmed/21295171
https://search.proquest.com/docview/866048192
https://search.proquest.com/docview/874182058
Volume 11
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