Effects of oral alpha-tocopherol on lung response in rat model of allergic asthma
Jazyk angličtina Země Austrálie Médium print
Typ dokumentu srovnávací studie, časopisecké články, práce podpořená grantem
    PubMed
          
           16771910
           
          
          
    DOI
          
           10.1111/j.1440-1843.2006.00864.x
           
          
          
      PII:  RES
  
    Knihovny.cz E-zdroje
    
  
              
      
- MeSH
 - aerosoly MeSH
 - alfa-tokoferol aplikace a dávkování terapeutické užití MeSH
 - aplikace orální MeSH
 - bronchiální astma farmakoterapie MeSH
 - bronchoalveolární lavážní tekutina chemie cytologie MeSH
 - krysa rodu Rattus MeSH
 - modely nemocí na zvířatech MeSH
 - ovalbumin imunologie MeSH
 - plíce účinky léků imunologie patologie MeSH
 - potkani Wistar MeSH
 - serotonin farmakologie MeSH
 - vztah mezi dávkou a účinkem léčiva MeSH
 - zvířata MeSH
 - Check Tag
 - krysa rodu Rattus MeSH
 - mužské pohlaví MeSH
 - zvířata MeSH
 - Publikační typ
 - časopisecké články MeSH
 - práce podpořená grantem MeSH
 - srovnávací studie MeSH
 - Názvy látek
 - aerosoly MeSH
 - alfa-tokoferol MeSH
 - ovalbumin MeSH
 - serotonin MeSH
 
OBJECTIVE AND BACKGROUND: Asthma is a chronic inflammatory disease in which an oxidant/antioxidant imbalance plays an important role. d-alpha-tocopherol (biologically the most active form of vitamin E) has redox properties and by scavenging the free radicals can act as an antioxidant. The aim of this study was to examine the effects of orally administered alpha-tocopherol in a rat model of allergic asthma. METHODOLOGY: Actively sensitized rats (OA) were treated with alpha-tocopherol (400 mg/kg/day for 10 days) or vehicle; 1 h after the last dose, they were challenged with antigen aerosol. The antigen-induced airway hyperresponsiveness to direct bronchoconstrictor (serotonin), the inflammatory cell infiltrate and histological changes were determined 1 or 24 h after the antigen challenge. RESULTS: Alpha-tocopherol pretreatment was not significantly effective at reducing the studied parameters when compared with controls, even though there was a tendency to a reduction in bronchial responsiveness and in eosinophil and neutrophil infiltration. CONCLUSION: Alpha-tocopherol when administered in the chosen study design in an animal model of asthma had no major effect on airway inflammation. The effect of antioxidants deserves further evaluation.
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