Am. J. Respir. Cell Mol. Biol., Vol 13, No. 2, Aug 1995, 133-143.
Effect of dexamethasone on antigen-induced high molecular weight glycoconjugate secretion in allergic guinea pigs
C Savoie, M Plant, M Zwikker, CJ van Staden, L Boulet, CC Chan, IW Rodger and DJ Pon
Merck Frosst Centre for Therapeutic Research, Kirkland, Quebec, Canada.
The ovalbumin-sensitized guinea pig is commonly used as a small animal
model of allergic asthma. This animal model exhibits many of the hallmark
characteristics observed in patients afflicted with asthma including
nonspecific airway hyperreactivity, airway eosinophilia, early and late
phase bronchoconstriction, and plasma extravasation into the airways. In
addition, mucous hypersecretion in the airways of asthmatic patients is
thought to be responsible for the plugging of distal airways and to
contribute to the morbidity and mortality associated with the disease
process. In this study we examined whether the allergic guinea pig model
exhibits an increase in airway high molecular weight glycoconjugate (HMWG)
secretion in response to an antigen challenge and whether dexamethasone
exerts any modulatory effects upon the response. Ovalbumin (OVA)
-sensitized guinea pigs were challenged with OVA 2 wk following the initial
exposure. Trachobronchoalveolar lavages (TBAL) were performed, and the
samples were assayed for total eosinophil cell number, eosinophil
peroxidase activity (EPO), and both acidic and neutral HMWG content.
Morphometric analysis of mucous-containing cells was also performed on
tissue sections prepared from the trachea, mainstem bronchus, and three
lobes of the left lung. Within 24 h of an antigen challenge, TBAL samples
obtained from the allergic guinea pigs exhibited increases in eosinophil
cell number, measured EPO enzyme activity, and acidic HMWG content compared
to TBAL samples prepared from vehicle-exposed animals. These
antigen-induced changes were dependent on the concentration of aerosolized
OVA administered. Exposing the animals to 0.3% OVA provoked a 6.23-fold
increase in airway eosinophils, 15-fold elevation in TBAL EPO enzyme
activity, and 175% increase in TBAL acidic HMWG. No significant changes in
TBAL neutral HMWG were measured. The changes in measured EPO activity
correlated with the levels of acidic HMWG found in the TBAL samples (r =
0.73, P < or = 0.001). The measured increase in TBAL acidic HMWG was
time dependent and was found to be maximal at 2 h post-antigen challenge.
Morphometric analysis of Alcian blue (pH 2.5) -stained airway sections
showed a decline in stored mucosubstances following the antigen exposure,
supporting the notion that the allergic guinea pig model exhibits a
mucosecretory component. Pretreating the animals with dexamethasone
attenuated the antigen-induced release of HMWG and changes in measured EPO
activity. In conclusion, these data indicate that the allergic guinea pig
may be a useful model for examining the neural and cellular mechanisms
underlying mucus hypersecretion in individuals afflicted with bronchial
asthma.
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Copyright © 1995 American Thoracic Society.
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