Suppressive Activity of Epinastine Hydrochloride on Eosinophil Activation In Vitro
The influence of a histamine H 1 receptor antagonist, epinastine hydrochloride (EP), on eosinophil functions was examined in vitro and in vivo. The first set of experiments was undertaken to examine whether EP could suppress eosinophilia and IgE hyperproduction induced by Mesocestoides cortii infect...
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Veröffentlicht in: | In vivo (Athens) 2008-01, Vol.22 (1), p.13-20 |
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Zusammenfassung: | The influence of a histamine H 1 receptor antagonist, epinastine hydrochloride (EP), on eosinophil functions was examined in vitro and in vivo. The first
set of experiments was undertaken to examine whether EP could suppress eosinophilia and IgE hyperproduction induced by Mesocestoides
cortii infection in BALB/c mice. The number of peripheral blood eosinophils and levels of IgE were examined 21 days after
infection. Oral administration of EP at a daily dose of 0.3 mg/kg, which is the recommended human therapeutic dose, for 21
days was not able to suppress either peripheral blood eosinophilia or IgE hyperproduction, which was observed in mice infected
with M. cortii. The second part of the experiment was designed to examine the influence of EP on eosinophil activation induced
by stem cell factor (SCF) stimulation in vitro. Eosinophils were obtained from M. cortii-infected mice and stimulated with
SCF in the presence of different concentrations of EP for 24 h. The addition of EP into cell cultures suppressed eosinophil
activation induced by SCF stimulation as assessed by measuring the contents of acronym for Regulated upon Activation, Normal
T cell Expressed and presumably Secreted (RANTES), macrophage inflammatory protein-1beta (MIP-1β) and leukotriene C 4 (LTC 4 ) levels in culture supernatants. The minimum concentration of EP which caused significant suppression of factor productions
was 25 ng/ml, which is similar to the concentration in plasma after oral administration of the therapeutic dose in humans.
These results may suggest that EP exerts inhibitory effects on eosinophil activation and results in favorable modification
of the clinical status of allergic patients. |
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ISSN: | 0258-851X 1791-7549 |