The nasal antigen challenge model has proved useful in assessing the r
oles of inflammatory mediators in the clinical allergic response. Stud
ies using this model have revealed that the acute allergic response is
associated with increased concentrations of histamine, prostaglandin
D2 (PGD2), leukotrienes, tryptase, and kinins, and with increased TAME
-esterase activity. The effects of antihistamines on the clinical resp
onse and inhibition of mediator release have also been examined with t
his model. Premedication with terfenadine caused a marked reduction in
sneezing as well as decreased histamine release, kinin levels, and TA
ME-esterase activity. Levels of PGD2 also decreased, although not sign
ificantly. Release of leukotriene C4 (LTC4) was not affected by this a
gent. Terfenadine also reduced vascular permeability as reflected in d
ecreased albumin levels. In this model, cetirizine reduced sneezing, T
AME-esterase activity, and albumin levels, whereas histamine release a
nd PGD2 levels remained unaffected. Pretreatment with cetirizine resul
ted in significantly reduced levels of LTC4. Loratadine markedly, but
not significantly, inhibited the sneezing response and reduced release
of histamine, PGD2, and LTC4. Albumin and kinin levels were significa
ntly diminished, The clinical significance of the inhibitory effects o
f antihistamines on mediator release has yet to be determined.