|
|
||||||||
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
ENVIRONMENTAL, EXERCISE AND RESPIRATORY PHYSIOLOGY
Departments of 1Respiratory Diseases, 2Hematology and 3Diabetes and Metabolism and 4Medical Research Center, School of Medicine, Pontificia Universidad Católica de Chile; and 5Program of Pathology, Institute of Biomedical Sciences, Universidad de Chile, Santiago, Chile
Submitted 15 May 2007 ; accepted in final form 13 July 2007
Syrian Golden hamsters develop severe emphysema after a single intratracheal dose of elastase, whereas Sprague-Dawley rats exhibit mild emphysema with the same dose per kilogram body weight. We hypothesized that the development of severe emphysema is prevented in rats by the high serum level of
1-antitrypsin reported in rats, compared with hamsters, which provides for a high lung elastase inhibitory capacity (EIC). To explore this possibility, we challenged the antiprotease system of the rats by treating them with three similar weekly doses of elastase. Four months after treatment, we evaluated changes in histology, volume, and elastic properties of rat lungs and compared them with those of hamsters receiving a single dose of elastase. We also measured serum
1-antitrypsin levels and serum and lung EIC in control rats and hamsters. Results showed that, in association with 40% less serum and lung EIC compared with rats (P < 0.001), hamster lungs had upper-lobe bullae formation, severe microscopic emphysema, a fourfold increase in lung volume (P < 0.01) and a threefold increase in constant k, an index of compliance, of the lung deflation pressure-volume curve (P < 0.01). In contrast, rats developed mild emphysema, with only 50% increase in volume (P < 0.05) and 60% increase in constant k (P < 0.01). In conclusion, two species that differ in serum and lung EIC exhibit significant differences in emphysema development after elastase. Rats with high EIC, despite receiving three doses of elastase, showed significantly less derangement of morphological and physiological parameters than hamsters with low EIC receiving a single dose.
alpha1-antitrypsin; disease models; lung mechanics; susceptibility
This article has been cited by other articles:
![]() |
G. R. Borzone, L. F. Liberona, A. P. Bustamante, C. G. Saez, P. R. Olmos, A. Vecchiola, A. Villagran, C. Serrano, and T. P. Reyes Differences in lung glutathione metabolism may account for rodent susceptibility in elastase-induced emphysema development Am J Physiol Regulatory Integrative Comp Physiol, April 1, 2009; 296(4): R1113 - R1123. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| Visit Other APS Journals Online |