, 1984). Interestingly, in the present study, the control group presented a similar proportion of epithelial ciliated cells to what has been described in human beings without respiratory disease. In addition, OVA-induced airway allergic inflammation decreased the volume proportion
of epithelial ciliated cells and increased the volume proportion of goblet cells, a pattern that has been previously described in asthmatic patients (Knight and Holgate, 2003, Lumsden et al., 1984 and Spina, 1998). In the present study, we also observed that aerobic exercise (AE), in either non-sensitized or sensitized animals, increased the number of epithelial cells and decreased the number of ciliated cells in BAL fluid, phenomena previously elegantly demonstrated in non-sensitized animals Chimenti et al. learn more (2007). In this study, the authors also demonstrated that although AE increased the apoptosis of epithelial cells, the stimulus for epithelial proliferation was higher, resulting in a positive
balance or turnover of airway epithelial cells (Chimenti et al., 2007). Concerning the effects of AE on the airway epithelial cells of animals with allergic airway inflammation, we observed that although DAPT cell line AE decreased goblet cell hyperplasia, it did not modify mucus production (Fig. 1B). Although the functions of airway epithelium were initially described as protective, in the last few years, a variety of immunomodulatory effects have been attributed to these cells, i.e., the secretion of cytokines, chemokines, free radicals and growth factors (Bedard
and Krause, 2007, Boots et al., 2009, Bove et al., 2007, Broide et al., 2005, Dugger et al., 2009, Forteza et al., 2005, Pantano et al., 2008, Rennard et al., 2005 and van Wetering et al., 2007). In the present study, we demonstrate that AE in sensitized animals decreases OVA-induced epithelial expression of IL-4, IL-5, IL-13, CCL11, CCL5, adhesion molecules ICAM-1 and VCAM-1, iNOS and NF-kB. In addition, AE oxyclozanide increased the epithelial expression of anti-inflammatory cytokine IL-10 (Fig. 1). These results are extremely relevant, as AE reduces the epithelial expression of the main proteins involved in the inflammatory process in asthma, which are related to the eosinophilic and lymphocytic migration to the airways as well as to airway remodeling (Lilly et al., 1997, Puxeddu et al., 2006, van Wetering et al., 2007, Wilson et al., 2001 and Wong et al., 2006). In the present study, we also observed that AE reduced the epithelial expression of GP91phox and 3-nitrotyrosine and the peribronchial expression of 8-isoprostane (Fig. 3A). Increased levels of reactive oxygen (ROS) and nitrogen species (RNS) in asthma have been related with the release of pro-inflammatory and pro-fibrotic molecules through NF-kB activation (Bedard and Krause, 2007).