| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
American Journal of Pathology, Vol 136, 1259-1266, Copyright © 1990 by American Society for Investigative Pathology
REGULAR ARTICLES |
SH Randell, RR Mercer and SL Young
Department of Medicine, Durham Veterans Affairs Medical Center, North Carolina.
High inspired oxygen concentrations during the neonatal period profoundly inhibit rat lung development, an effect that is partly reversed during recovery in air. Persistent effects of neonatal hyperoxia on the size and number of alveoli or the structure of pulmonary capillaries have not been well defined. Using light and electron microscopic morphometry plus quantitative three-dimensional reconstructions of alveoli, we examined the lungs of 40-day-old rats that were exposed to more than 95% oxygen for the first 7 days after birth. Neonatal hyperoxia administered to rats resulted in abnormally enlarged air spaces at age 40 days. The fraction of the lung consisting of parenchyma was significantly increased and alveolar surface area was 13% lower than controls. There was an abnormal enlargement of alveolar ducts, which reduced by 24% the relative amount of air in the alveoli, compared to that in the alveolar ducts. The number of alveoli per lung and the mean volume of an alveolus were not different between the groups, but alveolar size class distributions were different, with significantly more very small and very large alveoli in 40-day-old rats after neonatal hyperoxia. By scanning electron microscopy, the alveolar surface of the exposed animals had a corrugated appearance, which was especially evident along alveolar ducts. Transmission electron microscopy revealed a greater density of capillaries, particularly in the alveolar regions close to terminal airways. Based on a random sample of the entire parenchymal region, capillary blood volume per cm2 of alveolar basal lamina was 18% greater. The results demonstrate that neonatal exposure to hyperoxia can cause abnormalities in the pulmonary alveolar and capillary structure of 40-day-old rats, and that these changes are similar to some features of broncho-pulmonary dysplasia.
This article has been cited by other articles:
![]() |
V. Balasubramaniam, A. M. Maxey, D. B. Morgan, N. E. Markham, and S. H. Abman Inhaled NO restores lung structure in eNOS-deficient mice recovering from neonatal hypoxia Am J Physiol Lung Cell Mol Physiol, July 1, 2006; 291(1): L119 - L127. [Abstract] [Full Text] [PDF] |
||||
![]() |
B. Thebaud, F. Ladha, E. D. Michelakis, M. Sawicka, G. Thurston, F. Eaton, K. Hashimoto, G. Harry, A. Haromy, G. Korbutt, et al. Vascular Endothelial Growth Factor Gene Therapy Increases Survival, Promotes Lung Angiogenesis, and Prevents Alveolar Damage in Hyperoxia-Induced Lung Injury: Evidence That Angiogenesis Participates in Alveolarization Circulation, October 18, 2005; 112(16): 2477 - 2486. [Abstract] [Full Text] [PDF] |
||||
![]() |
F. Ladha, S. Bonnet, F. Eaton, K. Hashimoto, G. Korbutt, and B. Thebaud Sildenafil Improves Alveolar Growth and Pulmonary Hypertension in Hyperoxia-induced Lung Injury Am. J. Respir. Crit. Care Med., September 15, 2005; 172(6): 750 - 756. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. P. Jankov, X. Luo, A. Campbell, R. Belcastro, J. Cabacungan, L. Johnstone, H. Frndova, S. J. Lye, and A. K. Tanswell Fibroblast Growth Factor Receptor-1 and Neonatal Compensatory Lung Growth after Exposure to 95% Oxygen Am. J. Respir. Crit. Care Med., June 1, 2003; 167(11): 1554 - 1561. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. N. Ahmed, H. B. Suliman, R. J. Folz, E. Nozik-Grayck, M. L. Golson, S. N. Mason, and R. L. Auten Extracellular Superoxide Dismutase Protects Lung Development in Hyperoxia-exposed Newborn Mice Am. J. Respir. Crit. Care Med., February 1, 2003; 167(3): 400 - 405. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Koyama, E. Sato, A. Tsukadaira, M. Haniuda, H. Numanami, M. Kurai, S. Nagai, and T. Izumi Vascular endothelial growth factor mRNA and protein expression in airway epithelial cell lines in vitro Eur. Respir. J., December 1, 2002; 20(6): 1449 - 1456. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. S. Manji, C. J. O'Kelly, W. I. Leung, and D. M. Olson Timing of hyperoxic exposure during alveolarization influences damage mediated by leukotrienes Am J Physiol Lung Cell Mol Physiol, October 1, 2001; 281(4): L799 - L806. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. A. McGrath-Morrow and J. Stahl Apoptosis in Neonatal Murine Lung Exposed to Hyperoxia Am. J. Respir. Cell Mol. Biol., August 1, 2001; 25(2): 150 - 155. [Abstract] [Full Text] [PDF] |
||||
![]() |
R. L. Auten Jr., S. N. Mason, D. T. Tanaka, K. Welty-Wolf, and M. H. Whorton Anti-neutrophil chemokine preserves alveolar development in hyperoxia-exposed newborn rats Am J Physiol Lung Cell Mol Physiol, August 1, 2001; 281(2): L336 - L344. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Jakkula, T. D. Le Cras, S. Gebb, K. P. Hirth, R. M. Tuder, N. F. Voelkel, and S. H. Abman Inhibition of angiogenesis decreases alveolarization in the developing rat lung Am J Physiol Lung Cell Mol Physiol, September 1, 2000; 279(3): L600 - L607. [Abstract] [Full Text] [PDF] |
||||
![]() |
J.-R. Tang, T. D. le Cras, K. G. Morris Jr., and S. H. Abman Brief perinatal hypoxia increases severity of pulmonary hypertension after reexposure to hypoxia in infant rats Am J Physiol Lung Cell Mol Physiol, February 1, 2000; 278(2): L356 - L364. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. A. McGrath Induction of p21WAF/CIP1 during Hyperoxia Am. J. Respir. Cell Mol. Biol., February 1, 1998; 18(2): 179 - 187. [Abstract] [Full Text] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |