Résumé
Volatile oil of C. deodara, administered orally at the doses of 50, 100 and 200 mg/kg body weight, significantly inhibited the pedal edema induced by compound 48/80 in rats. The oil significantly inhibited compound 48/80 induced degranulation of isolated rat peritoneal mast cells at concentrations ranging from 25-200 micrograms/ml. C. deodara wood oil also significantly inhibited the enzyme lipoxygenase at a concentration of 200 micrograms/ml. Thus, the anti-inflammatory activity of C. deodara wood oil could be attributed to its mast cell stabilizing activity and the inhibition of leukotriene synthesis.
Sujets)
Animaux , Anti-inflammatoires non stéroïdiens/administration et posologie , Dégranulation cellulaire/effets des médicaments et des substances chimiques , Oedème/induit chimiquement , Inhibiteurs de la lipoxygénase/administration et posologie , Mâle , Mastocytes/effets des médicaments et des substances chimiques , Huiles végétales/administration et posologie , Rats , Rat Wistar , Arbres , 4-Méthoxyphénéthyl-méthyl-amine/toxicitéRésumé
Recent reports have indicated the effectiveness of furosemide in inhibiting responses to inhaled allergen and in treating allergic conjunctivitis. In the present study furosemide was tested for its antiallergic potential using compound 48/80 induced paw edema and in vitro mast cell degranulation. Furosemide was found to significantly inhibit compound 48/80 paw edema and compound 48/80 induced histamine release. Furosemide was also found to inhibit histamine release during passive peritoneal anaphylaxis in rats. The results suggest that furosemide may be inhibiting the release of mediators of anaphylaxis from the mast cells.