Journal of Applied Physiology Fuel your research with LabChart
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


J Appl Physiol 48: 643-647, 1980;
8750-7587/80 $5.00
This Article
Right arrow Full Text (PDF)
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 Email 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 Download to citation manager
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Sosenko, I. R.
Right arrow Articles by Frantz, I. D.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Sosenko, I. R.
Right arrow Articles by Frantz, I. D., 3rd

Journal of Applied Physiology, Vol 48, Issue 4 643-647, Copyright © 1980 by American Physiological Society


ARTICLES

Functional delay in lung maturation in fetuses of diabetic rabbits

I. R. Sosenko, E. E. Lawson, V. Demottaz and I. D. Frantz 3rd

Lung maturation was studied in fetuses of rabbits made diabetic with alloxan. Lung maturation was examined functionally with pressure-volume curves and by determining surfactant content of lung lavage on a surface balance, and biochemically by measuring disaturated phosphatidylcholine content (DSPC) and lecithin: sphingomyelin ratio (L/S) of lung lavage and DSPC content of lung tissue. Pressure-volume curves of 27.5-day fetuses of diabetic does demonstrated less deflation stability. Functional assessment of pulmonary lavage surfactant measured on a surface balance was less in diabetic fetuses at both 27.5 and 29.5 days of gestation. There were no differences in DSPC content or L/S of lung wash or DSPC in whole-lung tissue between diabetic and control fetuses. The discordance between surfactant function and concentrations of major surfactant phospholipids suggests that surfactant in fetuses of diabetic animals is qualitatively different from that in the normal fetus. These findings may explain why analysis of amniotic fluid phospholipid content sometimes fails to predict risk of respiratory distressed syndrome correctly in human diabetic pregnancies.





HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Visit Other APS Journals Online