PEDIATRICS Vol. 64 No. 5 November 1979, pp. 722-725
This Article
Right arrow Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Services
Right arrow E-mail this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My File Cabinet
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via CrossRef
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Ambruso, D. R.
Right arrow Articles by Johnston, R. B.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Ambruso, D. R.
Right arrow Articles by Johnston, R. B., Jr

Defective Oxidative Metabolism in Newborn Neutrophils: Discrepancy between Superoxide Anion and Hydroxyl Radical Generation

Daniel R. Ambruso MD1, Karl M. Altenburger MD1, and Richard B. Johnston Jr MD1

1 Departments of Pediatrics, National Jewish Hospital and Research Center and the University of Colorado School of Medicine, Denver

Investigation of oxidative metabolism in neutrophils (PMNs) from newborns was performed by measuring generation of superoxide anion (.O2-) and production of hydroxyl radical (.OH) in the resting state and after stimulation with opsonized zymosan or phorbol myristate acetate (PMA). Neutrophils from cord blood of ten term infants and normal adult controls were tested simultaneously. Cord PMNs generated significantly more .O2- than paired adult controls when stimulated with opsonized zymosan (P <.01) and produced less .OH with PMA (P <. 005). When the amount of .O2- and .OH released by newborn PMNs with both stimuli was expressed as percent of values obtained from paired adult controls, there was a discrepancy in the generation of these two radicals: newborn PMNs produced relatively less. OH compared to .O2-. This decreased ability to produce .OH could underlie defective bactericidal activity in PMNs of neonates.




This article has been cited by other articles:


Home page
NeoReviewsHome page
F. Urlichs and C. P. Speer
Neutrophil Function in Preterm and Term Infants
NeoReviews, October 1, 2004; 5(10): e417 - e430.
[Full Text] [PDF]


Home page
Infect. Immun.Home page
A. Ganer, E. Brummer, and D. A. Stevens
Correlation of Susceptibility of Immature Mice to Fungal Infection (Blastomycosis) and Effector Cell Function
Infect. Immun., December 1, 2000; 68(12): 6833 - 6839.
[Abstract] [Full Text] [PDF]


Home page
J Intensive Care MedHome page
T. E. Harper and R. D. Christensen
Bacterial Sepsis in the Newborn Infant: Developmental Deficiencies in Neutrophils and the Role of Neutrophil Transfusion
J Intensive Care Med, September 1, 1987; 2(5): 279 - 291.
[Abstract] [PDF]