On the pulmonary toxicity of oxygen : III. The induction of oxygen dependency by oxygen use
On the pulmonary toxicity of oxygen : III. The induction of oxygen dependency by oxygen use
Date
2010-05
Authors
Shanklin, D. Radford
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Keywords
Oxygen toxicity
Lung injury
Metabolic dependency
Respiratory distress syndrome
Hyaline membrane disease
Bilateral cervical vagotomy
Animal models for human disease
Semi-log graphics
Area under the curve analysis
Lung injury
Metabolic dependency
Respiratory distress syndrome
Hyaline membrane disease
Bilateral cervical vagotomy
Animal models for human disease
Semi-log graphics
Area under the curve analysis
Abstract
Oxygen is central to the development of neonatal lung injury. The increase in oxygen exposure of
the neonatal lung during the onset of extrauterine air breathing is an order of magnitude, from a
range of 10-12 to 110-120 Torr. The contributions of oxygen and the volume and pressure
relationships of ventilatory support to lung injury are not easily distinguished in the clinical setting.
Sequential changes in inspired air or 100% oxygen were studied in 536 newborn rabbits without
ventilatory support. Bilateral cervical vagotomies (BCV) were performed at 24 hours post natal to
induce ventilatory distress which eventuates in hyaline membrane disease. The sequences applied
yielded evidence for an induced state of oxygen dependency from oxygen use which was reflected
in differences in survival and the extent of pulmonary injury. The median survival for animals kept
in air throughout was 3 hours. Oxygen before vagotomy or during the first 3 hours afterwards
extended the survival significantly but produced more extensive, more severe, and more rapid lung
lesions. Returning animals to air after prior oxygen exposure reduced the number of survivors past
10 hours and shortened the maximum survival in those groups. These features indicate the
development of a dependency of the defense mechanisms on the availability of oxygen at the higher
level for metabolic and possibly other aspects of the pulmonary and systemic response to injury,
beyond the usual physiological need. Subset analysis revealed additive and latent effects of
oxygen and demonstrated a remarkable rapidity in onset of severe lesions under some
circumstances, illustrating the toxicity of oxygen per se.
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Author Posting. © The Author(s), 2010. This is the author's version of the work. It is posted here by permission of Elsevier B.V. for personal use, not for redistribution. The definitive version was published in Experimental and Molecular Pathology 89 (2010): 36-45, doi:10.1016/j.yexmp.2010.05.004.