Canadian Journal of Physiology and Pharmacology · 2010 · 31 citations · 19 references
MedicineImmunologyPharmacologyAllergyImmunoregulationInflammationAnti-inflammatory PharmacologyAsthma PharmacotherapyInflammation PharmacologyPulmonary InflammationRespiratory AllergyRespiratory PharmacologyAirway Inflammation ModulationAllergic Airway InflammationAnti-inflammatory ActivityAsthma ModelsEosinophil CountEosinophilic Lung InflammationMurine ModelsSerum Total Immunoglobulin E
Paeonol, the main active component isolated from Moutan Cortex, possesses extensive pharmacological activities such as anti-inflammatory, anti-allergic, and immunoregulatory effects. In the present study, we examined the effects of paeonol on airway inflammation and hyperresponsiveness in a mouse model of allergic asthma. BALB/c mice sensitized and challenged with ovalbumin were administered paeonol intragastrically at a dose of 100 mg/kg daily. Paeonol significantly suppressed ovalbumin-induced airway hyperresponsiveness to acetylcholine chloride. Paeonol administration significantly inhibited the total inflammatory cell and eosinophil count in bronchoalveolar lavage fluid. Treatment with paeonol significantly enhanced IFN-γ levels and decreased interleukin-4 and interleukin-13 levels in bronchoalveolar lavage fluid and total immunoglobulin E levels in serum. Histological examination of lung tissue demonstrated that paeonol significantly attenuated allergen-induced lung eosinophilic inflammation and mucus-producing goblet cells in the airway. These data suggest that paeonol exhibits anti-inflammatory activity in allergic mice and may possess new therapeutic potential for the treatment of allergic bronchial asthma.
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Requirement for IL-13 Independently of IL-4 in Experimental Asthma
Gabriele Grünig, Martha L. Warnock, Adil E. Wakil et al. · Science · 1998 · 1.9K citations
Defining a Link with Asthma in Mice Congenitally Deficient in Eosinophils
James J. Lee, Dawn Dimina, MiMi P. Macias et al. · Science · 2004 · 710 citations
IL-4 is required to generate and sustain in vivo IgE responses.
Fred D. Finkelman, Ildy M. Katona, Joseph F. Urban et al. · The Journal of Immunology · 1988 · 679 citations · Full text