Treatment with cyclosporin A during sensitization with trimellitic anhydride attenuates the airway responses to allergen challenge three weeks later
(1994) In European Journal of Pharmacology 252(3). p.313-319- Abstract
 - The present studies examined the effects of oral treatment with cyclosporin A, betamethasone or azelastine administered over the time of sensitization with trimellitic anhydride on allergen-induced airway responses, compared to those of control animals given corn oil alone. Drugs were given for 8 days. The animals were sensitized with trimellitic anhydride (0.1 ml of 0.3% w/v) in corn oil given intradermally on days 4 and 5 of drug treatment. Three to four weeks after sensitization with free trimellitic anhydride, the animals were anesthetized, tracheostomized and challenged with trimellitic anhydride conjugated to guinea pig serum albumin (trimellitic anhydride-guinea pig serum albumin; 0.5%; 50 microliters) instilled via the airway... (More)
 - The present studies examined the effects of oral treatment with cyclosporin A, betamethasone or azelastine administered over the time of sensitization with trimellitic anhydride on allergen-induced airway responses, compared to those of control animals given corn oil alone. Drugs were given for 8 days. The animals were sensitized with trimellitic anhydride (0.1 ml of 0.3% w/v) in corn oil given intradermally on days 4 and 5 of drug treatment. Three to four weeks after sensitization with free trimellitic anhydride, the animals were anesthetized, tracheostomized and challenged with trimellitic anhydride conjugated to guinea pig serum albumin (trimellitic anhydride-guinea pig serum albumin; 0.5%; 50 microliters) instilled via the airway route. In the same animal, we measured both lung resistance (RL) to monitor airflow obstruction, and extravasation of Evans Blue dye (20 mg/kg) to quantify airway plasma exudation. In control animals, instillation of trimellitic anhydride-guinea pig serum albumin into the tracheal lumen caused a slowly progressing increase in RL over the observation period (6 min), in addition to extravasation of Evans Blue dye at all airway levels. In animals treated with 50 mg/kg of cyclosporin A, both the allergen-induced increase in RL and extravasation of Evans Blue dye in intrapulmonary airways were significantly attenuated. However, neither betamethasone nor azelastine significantly affected these responses. We conclude that cyclosporin A may influence the immune system in the guinea pig during the induction of allergy, thus leading to attenuation of allergen-induced airway obstruction at later time points. (Less)
 
    Please use this url to cite or link to this publication:
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- author
 - Arakawa, H ; Andius, P ; Kawikova, I ; Skoogh, B E ; Löfdahl, Claes-Göran LU and Lotvall, J
 - publishing date
 - 1994
 - type
 - Contribution to journal
 - publication status
 - published
 - subject
 - keywords
 - Asthma, Anhydride, Allergy, Cyclosporin A, Glucocorticoid, Sensitization
 - in
 - European Journal of Pharmacology
 - volume
 - 252
 - issue
 - 3
 - pages
 - 313 - 319
 - publisher
 - Elsevier
 - external identifiers
 - 
                
- pmid:7909293
 - scopus:0028137899
 
 - ISSN
 - 1879-0712
 - DOI
 - 10.1016/0014-2999(94)90178-3
 - language
 - English
 - LU publication?
 - no
 - id
 - 5b39e3b2-21d0-4369-9f37-6f50a326ac71 (old id 1108313)
 - date added to LUP
 - 2016-04-01 12:02:11
 - date last changed
 - 2025-10-14 09:45:43
 
@article{5b39e3b2-21d0-4369-9f37-6f50a326ac71,
  abstract     = {{The present studies examined the effects of oral treatment with cyclosporin A, betamethasone or azelastine administered over the time of sensitization with trimellitic anhydride on allergen-induced airway responses, compared to those of control animals given corn oil alone. Drugs were given for 8 days. The animals were sensitized with trimellitic anhydride (0.1 ml of 0.3% w/v) in corn oil given intradermally on days 4 and 5 of drug treatment. Three to four weeks after sensitization with free trimellitic anhydride, the animals were anesthetized, tracheostomized and challenged with trimellitic anhydride conjugated to guinea pig serum albumin (trimellitic anhydride-guinea pig serum albumin; 0.5%; 50 microliters) instilled via the airway route. In the same animal, we measured both lung resistance (RL) to monitor airflow obstruction, and extravasation of Evans Blue dye (20 mg/kg) to quantify airway plasma exudation. In control animals, instillation of trimellitic anhydride-guinea pig serum albumin into the tracheal lumen caused a slowly progressing increase in RL over the observation period (6 min), in addition to extravasation of Evans Blue dye at all airway levels. In animals treated with 50 mg/kg of cyclosporin A, both the allergen-induced increase in RL and extravasation of Evans Blue dye in intrapulmonary airways were significantly attenuated. However, neither betamethasone nor azelastine significantly affected these responses. We conclude that cyclosporin A may influence the immune system in the guinea pig during the induction of allergy, thus leading to attenuation of allergen-induced airway obstruction at later time points.}},
  author       = {{Arakawa, H and Andius, P and Kawikova, I and Skoogh, B E and Löfdahl, Claes-Göran and Lotvall, J}},
  issn         = {{1879-0712}},
  keywords     = {{Asthma; Anhydride; Allergy; Cyclosporin A; Glucocorticoid; Sensitization}},
  language     = {{eng}},
  number       = {{3}},
  pages        = {{313--319}},
  publisher    = {{Elsevier}},
  series       = {{European Journal of Pharmacology}},
  title        = {{Treatment with cyclosporin A during sensitization with trimellitic anhydride attenuates the airway responses to allergen challenge three weeks later}},
  url          = {{http://dx.doi.org/10.1016/0014-2999(94)90178-3}},
  doi          = {{10.1016/0014-2999(94)90178-3}},
  volume       = {{252}},
  year         = {{1994}},
}