Literature DB >> 10686510

Sequential development of airway hyperresponsiveness and acute airway obstruction in a mouse model of allergic inflammation.

U Neuhaus-Steinmetz1, T Glaab, A Daser, A Braun, M Lommatzsch, U Herz, J Kips, Y Alarie, H Renz.   

Abstract

BACKGROUND: Mouse models have been established mirroring key features of human bronchial asthma including airway hyperresponsiveness (AHR). Acute airway obstruction in response to an allergen challenge, however, remains to be demonstrated in these models.
OBJECTIVE: A mouse model of allergic lung inflammation was employed to analyze the development of specific (allergen-induced) and nonspecific (methacholine-induced) airway obstruction.
METHODS: Mice were sensitized to ovalbumin (OVA) and challenged with OVA aerosol twice each week during four weeks. Changes in lung functions were determined by noninvasive head-out body plethysmography. The development of acute airway obstruction after OVA challenge and AHR after methacholine aerosol application were assessed by a decrease in the mid-expiratory flow rate (EF(50)).
RESULTS: Two airway challenges were sufficient to induce AHR (5.7 vs. 15 mg/ml methacholine). Further OVA challenges reduced the baseline EF(50) from 1.85 to 1.20 ml/s (4th week) and induced acute airway obstruction. The OVA-induced obstruction was maximal in the 4th week (EF(50) = 0.91 ml/s).
CONCLUSION: The development of acute airway obstruction in allergen-sensitized mice was demonstrated by means of head-out body plethysmography. In our model, AHR was observed before the development of airway obstruction. Copyright 2000 S. Karger AG, Basel

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Year:  2000        PMID: 10686510     DOI: 10.1159/000024298

Source DB:  PubMed          Journal:  Int Arch Allergy Immunol        ISSN: 1018-2438            Impact factor:   2.749


  16 in total

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2.  A leak-free head-out plethysmography system to accurately assess lung function in mice.

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4.  Maternal TLR signaling is required for prenatal asthma protection by the nonpathogenic microbe Acinetobacter lwoffii F78.

Authors:  Melanie L Conrad; Ruth Ferstl; René Teich; Stephanie Brand; Nicole Blümer; Ali O Yildirim; Cecilia C Patrascan; Anna Hanuszkiewicz; Shizuo Akira; Hermann Wagner; Otto Holst; Erika von Mutius; Petra I Pfefferle; Carsten J Kirschning; Holger Garn; Harald Renz
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5.  Brain-derived neurotrophic factor (BDNF) contributes to neuronal dysfunction in a model of allergic airway inflammation.

Authors:  Armin Braun; Marek Lommatzsch; Ulrich Neuhaus-Steinmetz; David Quarcoo; Thomas Glaab; Gerard P McGregor; Axel Fischer; Harald Renz
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6.  Lung function measurements in rodents in safety pharmacology studies.

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7.  Invasive versus noninvasive measurement of allergic and cholinergic airway responsiveness in mice.

Authors:  Thomas Glaab; Michaela Ziegert; Ralf Baelder; Regina Korolewitz; Armin Braun; Jens M Hohlfeld; Wayne Mitzner; Norbert Krug; Heinz G Hoymann
Journal:  Respir Res       Date:  2005-11-25

8.  Comparison of adjuvant and adjuvant-free murine experimental asthma models.

Authors:  M L Conrad; A O Yildirim; S S Sonar; A Kiliç; S Sudowe; M Lunow; R Teich; H Renz; H Garn
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9.  Targeted delivery of siRNA to activated T cells via transferrin-polyethylenimine (Tf-PEI) as a potential therapy of asthma.

Authors:  Yuran Xie; Na Hyung Kim; Venkatareddy Nadithe; Dana Schalk; Archana Thakur; Ayşe Kılıç; Lawrence G Lum; David J P Bassett; Olivia M Merkel
Journal:  J Control Release       Date:  2016-03-19       Impact factor: 9.776

10.  OVA-induced airway hyperresponsiveness alters murine heart rate variability and body temperature.

Authors:  N J Domnik; G Seaborn; S G Vincent; S G Akl; D P Redfearn; J T Fisher
Journal:  Front Physiol       Date:  2012-12-04       Impact factor: 4.566

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