Literature DB >> 8420402

Leukotrienes in bile during the early and the late airway responses after allergen challenge of sensitized rats.

J G Martin1, L J Xu, M Y Toh, R Olivenstein, W S Powell.   

Abstract

The Brown Norway rat produces high levels of IgE in response to active immunization and develops both early and late airway constrictor responses after subsequent allergen challenge. We have used this model of allergic asthma to investigate the temporal relationship between the in vivo synthesis of peptidoleukotrienes (peptido-LTs) and the late response. Brown Norway rats that had been sensitized by injection of ovalbumin 2 to 3 wk prior to the commencement of the experiment were subjected to bile duct cannulation and tracheal intubation. The rats were challenged 2 h later by intratracheal instillation of ovalbumin. Lung resistance was measured before and at frequent intervals after antigen challenge. Biliary peptido-LTs (LTC4, LTD4, LTE4, and N-acetyl-LTE4) were measured by a combination of high pressure liquid chromatography and radioimmunoassay in bile samples collected for a period of 1 h before instillation of ovalbumin, and between zero and 1 h, 1 and 4 h, 4 and 6 h, and 6 and 8 h, subsequently. All of the 10 rats subjected to antigen challenge developed early responses. Of these, six also developed late responses, whereas two died about 1 h after challenge. The levels of peptido-LTs excreted in bile between 4 and 8 h after antigen challenge (corresponding in time to the late responses) were about four times higher in the ovalbumin-instilled rats that developed late responses (n = 6) than in the ovalbumin-sensitized control rats that had been subjected to instillation of saline (n = 6; p < 0.02).(ABSTRACT TRUNCATED AT 250 WORDS)

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Year:  1993        PMID: 8420402     DOI: 10.1164/ajrccm/147.1.104

Source DB:  PubMed          Journal:  Am Rev Respir Dis        ISSN: 0003-0805


  7 in total

1.  A small molecule, orally active, alpha4beta1/alpha4beta7 dual antagonist reduces leukocyte infiltration and airway hyper-responsiveness in an experimental model of allergic asthma in Brown Norway rats.

Authors:  Julio Cortijo; María-Jesús Sanz; Arantxa Iranzo; José Luis Montesinos; Yafa Naim Abu Nabah; José Alfón; Luis A Gómez; Manuel Merlos; Esteban J Morcillo
Journal:  Br J Pharmacol       Date:  2006-03       Impact factor: 8.739

2.  Involvement of cysteinyl leukotrienes in airway smooth muscle cell DNA synthesis after repeated allergen exposure in sensitized Brown Norway rats.

Authors:  M Salmon; D A Walsh; T J Huang; P J Barnes; T B Leonard; D W Hay; K F Chung
Journal:  Br J Pharmacol       Date:  1999-07       Impact factor: 8.739

3.  Mast-cell activation augments the late phase reaction in experimental immune-mediated blepharoconjunctivitis.

Authors:  Akemi Ozaki; Atsuki Fukushima; Kazuyo Fukata; Hisayuki Ueno
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  2003-04-04       Impact factor: 3.117

4.  Transfer of allergic airway responses with antigen-primed CD4+ but not CD8+ T cells in brown Norway rats.

Authors:  A Watanabe; H Mishima; P M Renzi; L J Xu; Q Hamid; J G Martin
Journal:  J Clin Invest       Date:  1995-09       Impact factor: 14.808

5.  Allergen-induced airway responses in rats pretreated with Sephadex.

Authors:  P Rossi; L Xu; N S Wang; J G Martin
Journal:  Agents Actions       Date:  1993-11

6.  The strength of the OVA-induced airway inflammation in rats is strain dependent.

Authors:  M N Hylkema; M O Hoekstra; M Luinge; W Timens
Journal:  Clin Exp Immunol       Date:  2002-09       Impact factor: 4.330

7.  Site of allergic airway narrowing and the influence of exogenous surfactant in the Brown Norway rat.

Authors:  Sana Siddiqui; Kimitake Tsuchiya; Paul-André Risse; Sharon R Bullimore; Andrea Benedetti; James G Martin
Journal:  PLoS One       Date:  2012-01-19       Impact factor: 3.240

  7 in total

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