Published 2005

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Publication details

Journal : Pediatric Research , vol. 58 , p. 542–548 , 2005

International Standard Numbers :
Printed : 0031-3998
Electronic : 1530-0447

Publication type : Academic article

Contributors : Munkeby, Berit Holthe; Børke, Wenche Bakken; Bjørnland, Kristin; Sikkeland, Liv Ingunn Bjoner; Borge, Grethe Iren Andersen; Lømo, Jon; Rivera, S; Khrestchatisky, M.; Halvorsen, Bente ; Saugstad, Ola Didrik

Issue : 3

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We hypothesized that resuscitation with 100% O(2) compared with 21% O(2) is detrimental to pulmonary tissue. The pulmonary injury was assessed by matrix metalloproteinase (MMP) activity, oxidative stress, IL-8, and histology 2.5 h after resuscitation from a hypoxic state. In pulmonary tissue extracts, MMP activity was analyzed by broad matrix-degrading capacity (total MMP) and zymography. MMP-2 mRNA expression was evaluated by quantitative real-time PCR. Total endogenous antioxidant capacity was measured by the oxygen radical absorbance capacity (ORAC) assay, and IL-8 was analyzed by ELISA technique. In bronchoalveolar lavage (BAL) fluid, MMPs were analyzed by zymography. In pulmonary tissue, pro- and active MMP-2 levels were increased in piglets that were resuscitated with 100% O(2) compared with 21% O(2). Pro-MMP-9, total MMP activity, and MMP-2 mRNA levels were significantly increased in resuscitated piglets compared with baseline. Net gelatinolytic activity increased in submucosa and blood vessels after 100% O(2) and only in the blood vessels after 21% O(2). Compared with baseline, ORAC values were considerably lowered in the resuscitated piglets and significantly reduced in the 100% O(2) versus 21% O(2) group. In BAL fluid, both pro-MMP-9 and pro-MMP-2 increased 2-fold in the 100% O(2) group compared with 21% O(2). Moreover, IL-8 concentration increased significantly in piglets that were resuscitated with 100% O(2) compared with 21% O(2), suggesting a marked proinflammatory response in the pulmonary tissue. Altogether, these data strongly suggest that caution must be taken when applying pure O(2) to the newborn infant.