Meconium Aspiration Syndrome (MAS) is a cause of significant morbidity and mortality in the perinatal period and has been implicated in the pathogenesis of airway dysfunction. In this study, we developed a murine model to evaluate the effects of meconium aspiration on airway physiology and lung cellular responses. Under light anesthesia, Balb/c mice received a single intratracheal instillation of meconium or physiologic saline. Respiratory mechanics were measured in unrestrained animals and expressed as % increase in Penh to increasing concentrations of methacholine (Mch). Furthermore, we assessed the changes in cells and cytokines into the bronchoalveolar lavage fluid (BALF). We found meconium aspiration produced increased airway responsiveness to Mch at 7 days. These functional changes were associated with lymphocytic/eosinophilic inflammation, goblet cell metaplasia and increased concentrations of IL-5 and IL-13 in the BALF. Our findings suggest meconium aspiration leads to alterations of airway function, lung eosinophilia, goblet cell metaplasia and cytokine imbalance thus providing the first evidence of meconium-induced airway dysfunction in a mouse model.