Superoxide release and cellular gluthatione peroxidase activity in leukocytes from children with persistent asthma
UMass Chan Affiliations
Department of PediatricsDocument Type
Journal ArticlePublication Date
2004-11-01Keywords
AdolescentAsthma
Biological Markers
Case-Control Studies
Child
Chronic Disease
Female
Glutathione Peroxidase
Granulocytes
Humans
Male
Monocytes
Superoxide Dismutase
Time Factors
Hematology
Oncology
Pediatrics
Metadata
Show full item recordAbstract
Asthma is an inflammatory condition characterized by the involvement of several mediators, including reactive oxygen species. The aim of the present study was to investigate the superoxide release and cellular glutathione peroxidase (cGPx) activity in peripheral blood granulocytes and monocytes from children and adolescents with atopic asthma. Forty-four patients were selected and classified as having intermittent or persistent asthma (mild, moderate or severe). The spontaneous or phorbol myristate acetate (PMA, 30 nM)-induced superoxide release by granulocytes and monocytes was determined at 0, 5, 15, and 25 min. cGPx activity was assayed spectrophotometrically. The spontaneous superoxide release by granulocytes from patients with mild (N = 15), moderate (N = 12) or severe (N = 6) asthma was higher at 25 min compared to healthy individuals (N = 28, P andlt; 0.05, Duncan test). The PMA-induced superoxide release by granulocytes from patients with moderate (N = 12) or severe (N = 6) asthma was higher at 15 and 25 min compared to healthy individuals (N = 28, P andlt; 0.05 in both times of incubation, Duncan test). The spontaneous or PMA-induced superoxide release by monocytes from asthmatic patients was similar to healthy individuals (P > 0.05 in all times of incubation, Duncan test). cGPx activity of granulocytes and monocytes from patients with persistent asthma (N = 20) was also similar to healthy individuals (N = 10, P > 0.05, Kruskal-Wallis test). We conclude that, under specific circumstances, granulocytes from children with persistent asthma present a higher respiratory burst activity compared to healthy individuals. These findings indicate a risk of oxidative stress, phagocyte auto-oxidation, and the subsequent release of intracellular toxic oxidants and enzymes, leading to additional inflammation and lung damage in asthmatic children.Source
Braz J Med Biol Res. 2004 Nov;37(11):1607-13. Epub 2004 Oct 26. doi: 10.1590/S0100-879X2004001100003. Link to article on publisher's site
DOI
10.1590/S0100-879X2004001100003Permanent Link to this Item
http://hdl.handle.net/20.500.14038/43388PubMed ID
15517074Related Resources
Link to article in PubMedRights
All the contents of this journal, except where otherwise noted, are licensed under a Creative Commons Attribution License, http://creativecommons.org/licenses/by-nc/3.0/
ae974a485f413a2113503eed53cd6c53
10.1590/S0100-879X2004001100003
