Abstract
Airway epithelium plays important roles in the pathophysiology of asthma. Creatine
supplementation (Cr) was shown to increase asthma features in a murine model of allergic
asthma; however, the role of the airway epithelium in this inflammatory response is
not known. BALB/c mice were divided into control, creatine supplementation, ovalbumin-sensitized
(OVA) and OVA plus creatine supplementation groups. OVA sensitization occurred on
days 0, 14, 28 and 42, and ovalbumin challenge from days 21–53. Cr was also given
on days 21–53. Total and differential cells counts in BALF were evaluated. Quantitative
epithelial expression of interleukin (IL)-4, IL-5, IL-13, CCL11, CCL5, CCL2, iNOS,
VCAM-1, ICAM-1, NF-κB, VEGF, TGF-β, IGF-1, EGFR, TIMP-1, TIMP-2, MMP-9, MMP-12 and
arginase II were performed. Cr increased the number of total cells and eosinophils
in BALF, the epithelial content of goblet cells and the epithelial expression of IL-5,
CCL2, iNOS, ICAM-1, NF-κB, TGF-β, TIMP-1 and MMP-9 when compared to the control group
(p<0.05). Creatine supplementation also exacerbated goblet cell proliferation, and
IL-5 and iNOS expression by epithelial cells compared to the OVA group (p<0.01). Creatine
up-regulates the pro-inflammatory cascade and remodelling process in this asthma model
by modulating the expression of inflammatory mediators by epithelial cells.
Key words
creatine monohydrate - airway epithelium - cytokines - growth factors - allergy
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Correspondence
Dr. Rodolfo Paula Vieira
Albert-Ludwigs University of Freiburg, Pneumology
Breisacher Straße 5
79106 Freiburg
Germany
Phone: +49/761/270 6363
Fax: +49/761/270 6363
Email: rodrelena@yahoo.com.br