The effect of 5-lipoxygenase inhibition on Ascaris antigen (Ag)-induced responses in atopic monkeys
Autor: | W. B. Smith, J. F. Eggler, J. W. Watson, C R Turner, Catharine J. Andresen |
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Rok vydání: | 1996 |
Předmět: |
Male
Neutrophils Immunology Inflammation Pharmacology Quinolones Leukocyte Count In vivo medicine Animals Hydroxyurea Lipoxygenase Inhibitors Ascaris suum Whole blood Pyrans medicine.diagnostic_test biology Chemistry Anti-Inflammatory Agents Non-Steroidal Zileuton respiratory system biology.organism_classification Macaca fascicularis Bronchoalveolar lavage Antigens Helminth Arachidonate 5-lipoxygenase biology.protein medicine.symptom Bronchoalveolar Lavage Fluid Ex vivo medicine.drug |
Zdroj: | Inflammation research : official journal of the European Histamine Research Society ... [et al.]. 45(1) |
ISSN: | 1023-3830 |
Popis: | The effects of two 5-lipoxygenase (5LO) inhibitors, ZD2138 or Zileuton, on acute, inflammatory responses to aerosolized Ascaris suum (Ag) were determined in atopic Macaca fascicularis monkeys. Monkeys (n = 6 each group) were dosed with vehicle, 3 or 10 mg/kg ZD2138, or 30 mg/kg Zileuton (p.o.). Both ZD2138 or Zileuton significantly inhibited ex vivo LTB4 production in Ca2+ ionophore-stimulated whole blood from these same monkeys (n = 6 each group) by 45.5% (3 mg/kg ZD2138), 82.5% (10 mg/kg ZD2138) and 84.3% (30 mg/kg Zileuton). ZD2138 (10 mg/kg) reduced bronchoalveolar lavage (BAL) LTE4 levels (65.1% inhibition), BAL neutrophils (88.9% inhibition), and IL-6 (54.0% inhibition) 4h post Ag. Zileuton inhibited these responses and also reduced BAL levels of IL-8 (73.4% inhibition). A second study was performed to evaluate the effects of ZD2138 on chronic Ag-induced responses. Treatment with ZD2138 did not prevent pulmonary inflammation or the development of airway hyperresponsiveness (AHR). Based upon these results, 5LO inhibition significantly reduced ex vivo LTB4 and in vivo LTE4 production as well as several acute inflammatory responses to Ag in the lung. However, ZD2138 did not inhibit more chronic responses following multiple Ag exposure. |
Databáze: | OpenAIRE |
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