Pathologic changes in the lungs of oxygen-adapted rats: a morphometric analysis
- PMID: 739764
Pathologic changes in the lungs of oxygen-adapted rats: a morphometric analysis
Abstract
Animals exposed to 85 per cent O2 for 5 or more days acquire the ability to survive for prolonged periods in 100 per cent O2. The basis of this acquired "tolerance" is poorly understood, but it has been proposed to be related to biochemical changes occurring in the lung cells. In order to quantify the structural changes that occur in the lungs of oxygen-adapted rats, rats were exposed to 85 per cent O2 for 7 days and then studied using morphometric techniques. The oxygen-adapted rats had a normal number of alveolar type I epithelial cells and a moderate increase in the number of alveolar type II cells. The alveolar type I epithelium was intact over the entire alveolar surface and appeared to have a normal ultrastructure, whereas alveolar type II cells demonstrated occasional changes in mitochondrial structure. In the interstitial compartment, there was a large increase in the number of interstitial cells and a significant increase in the noncellular components of the interstitium. The major area of pulmonary damage occurred in the vascular compartment, where entire segments of the capillary bed were lost and the total number of endothelial cells decreased by 45 per cent. A significant change in pulmonary vascular hemodynamics was suggested by a 49 per cent decrease in total capillary lumen volume and a decrease in the hematocrit of blood in the pulmonary capillary lumen to 57 per cent of the value found in aortic blood.
Similar articles
-
Consequences of prolonged inhalation of ozone on F344/N rats: collaborative studies. Part VIII: Morphometric analysis of structural alterations in alveolar regions.Res Rep Health Eff Inst. 1995 Mar;(65 Pt 8-9):3-39; discussion 99-110. Res Rep Health Eff Inst. 1995. PMID: 7619333
-
Effects of inhalation of 0.12 and 0.25 parts per million ozone on the proximal alveolar region of juvenile and adult rats.Lab Invest. 1985 Dec;53(6):692-704. Lab Invest. 1985. PMID: 4068670
-
NTP Toxicology and Carcinogenesis Studies of Ozone (CAS No. 10028-15-6) and Ozone/NNK (CAS No. 10028-15-6/ 64091-91-4) in F344/N Rats and B6C3F1 Mice (Inhalation Studies).Natl Toxicol Program Tech Rep Ser. 1994 Oct;440:1-314. Natl Toxicol Program Tech Rep Ser. 1994. PMID: 12595923
-
Prevention of collagen deposition following pulmonary oxygen toxicity in the rat by cis-4-hydroxy-L-proline.J Clin Invest. 1980 Mar;65(3):643-51. doi: 10.1172/JCI109709. J Clin Invest. 1980. PMID: 6986411 Free PMC article. Review.
-
Application of morphometric methods to study diffuse and focal injury in the lung caused by toxic agents.Crit Rev Toxicol. 1985;14(1):1-32. doi: 10.3109/10408448509023763. Crit Rev Toxicol. 1985. PMID: 2578919 Review.
Cited by
-
Isolation of type II epithelial cells from rabbit fetal lungs by adherence on an IgG-coated surface.Experientia. 1996 Aug 15;52(8):799-802. doi: 10.1007/BF01923992. Experientia. 1996. PMID: 8774751
-
Human alveolar macrophage growth factor for fibroblasts. Regulation and partial characterization.J Clin Invest. 1982 Oct;70(4):806-22. doi: 10.1172/jci110677. J Clin Invest. 1982. PMID: 7119116 Free PMC article.
-
Endurance training and antioxidants of lung.Experientia. 1984 Aug 15;40(8):822-3. doi: 10.1007/BF01951971. Experientia. 1984. PMID: 6468585
-
Modulation of alveolar macrophage-driven fibroblast proliferation by alternative macrophage mediators.J Clin Invest. 1986 Mar;77(3):700-8. doi: 10.1172/JCI112364. J Clin Invest. 1986. PMID: 3081573 Free PMC article.
-
Proliferative changes in the pulmonary arterial wall during short-term hyperoxic injury to the lung.Am J Pathol. 1988 Sep;132(3):563-73. Am J Pathol. 1988. PMID: 3414783 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Other Literature Sources