PT - JOURNAL ARTICLE AU - YU-ICHIRO MOCHIZUKI AU - ATSUKO FURUTA AU - AYAKO FURUYA AU - KEN-ICHI KANAI AU - KAZUHITO ASANO AU - HARUMI SUZAKI TI - Suppressive Activity of Epinastine Hydrochloride on Eosinophil Activation <em>In Vitro</em> DP - 2008 Jan 01 TA - In Vivo PG - 13--20 VI - 22 IP - 1 4099 - http://iv.iiarjournals.org/content/22/1/13.short 4100 - http://iv.iiarjournals.org/content/22/1/13.full SO - In Vivo2008 Jan 01; 22 AB - The influence of a histamine H1 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 C4 (LTC4) 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. Copyright © 2008 International Institute of Anticancer Research (Dr. John G. Delinassios), All rights reserved