Document Detail


Effects of long-term exposures to 100% oxygen at selected simulated altitudes on the pulmonary surfactant in mice.
MedLine Citation:
PMID:  1172927     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
The purpose of this investigation was to evaluate the effects on pulmonary surfactant in mice after long-duration exposure to 100% oxygen at various partial pressures equivalent to 842 mb (632) mmHg) or less. Six-month-old female CBA mice, weighing 25-35 g, were exposed to the pure oxygen environment. The effect on pulmonary surfactant was evaluated in two groups of 16 experimental animals and compared with control groups which were maintained in a similar environmentally controlled chamber at sea level conditions. Group I was exposed to pure oxygen at 842 mb (632 mmHg), a level known to be toxic and lethal. Group II was initially exposed for 60 d to pure oxygen at 420 mb (315 mmHg), a level not expected to be lethal, and the oxygen partial pressure gradually increased in steps over a 150-d period until an oxygen partial pressure at 842 mb (632 mmHg) was reached. In Group I, 12 out of 16 mice died of respiratory distress within 7 d. One died on the 10th day and three survived to complete 15 d of exposure but were euthanized because of severe despiratory distress. Mice in Group II which were exposed to pregressively increasing oxygen partial pressures survived. Pulmonary surfactant was obtained by saline lavage of the lungs. Chloroform/methanol extracted samples from oxygen-exposed mice in Group I displayed lower surfactant activity than Group II or controls. In fact, surfactant activity of mice dying in respiratory distress after 7 d was markedly lower than that of all other animals. Mice in Group II exhibited significantly lower(p less than 0.05) surfactant activity than controls, X = 34.71 and 38.58 respectively. This lower surfactant activity was consistent for Group II throughout the 150-d exposure except at the 90-d and 150-d exposures. The findings of this investigation support preceding studies which contend that the lung is the most vulnerable target for oxygen toxicity at altitude. It appears that an adaptive process involving both quantitative and qualitative changes in the pulmonary surfactant enabled animals in Group II to survive the progressively increasing ocygen partial pressures in an environment where survival would not normally be possible.
Authors:
P J Sheffield
Related Documents :
9817717 - Heparin improves gas exchange during experimental acute lung injury in newborn piglets.
6954087 - Drug deposition of pressurized inhalation aerosols.
10501757 - The open lung concept: pressure-controlled ventilation is as effective as high-frequenc...
1172927 - Effects of long-term exposures to 100% oxygen at selected simulated altitudes on the pu...
2922577 - Pyeloureteral dynamics. pelvic pressure and kidney function in partial long-term ureter...
24946657 - Negative pressure and muscle activity during discrete sips from high resistance straws.
Publication Detail:
Type:  Journal Article    
Journal Detail:
Title:  Aviation, space, and environmental medicine     Volume:  46     ISSN:  0095-6562     ISO Abbreviation:  Aviat Space Environ Med     Publication Date:  1975 Jan 
Date Detail:
Created Date:  1975-05-19     Completed Date:  1975-05-19     Revised Date:  2003-11-14    
Medline Journal Info:
Nlm Unique ID:  7501714     Medline TA:  Aviat Space Environ Med     Country:  UNITED STATES    
Other Details:
Languages:  eng     Pagination:  6-10     Citation Subset:  IM; S    
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:
Animals
Atmosphere Exposure Chambers*
Atmospheric Pressure
Attitude*
Environment, Controlled
Female
Mice
Mice, Inbred CBA
Oxygen / toxicity*
Pulmonary Surfactants*
Surface Tension
Time Factors
Chemical
Reg. No./Substance:
0/Pulmonary Surfactants; 7782-44-7/Oxygen

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


Previous Document:  Clinical manifestations of splenic abscess.
Next Document:  Increased susceptibility to pulmonary oxygen toxicity after cholesterol biosynthesis inhibition.