|
|
||||||||
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Division of Physiology, Department of Environmental Health Sciences, The Johns Hopkins University Bloomberg School of Public Health, Baltimore, Maryland
Submitted 8 July 2005 ; accepted in final form 8 November 2005
Previous work by our group has demonstrated substantial differences in lung volume and morphometric parameters between inbred mice. Specifically, adult C3H/HeJ (C3) have a 50% larger lung volume and 30% greater mean linear intercept than C57BL/6J (B6) mice. Although much of lung development occurs postnatally in rodents, it is uncertain at what age the differences between these strains become manifest. In this study, we performed quasi-static pressure-volume curves and morphometric analysis on neonatal mice. Lungs from anesthetized mice were degassed in vivo using absorption of 100% O2. Pressure-volume curves were then recorded in situ. The lungs were then fixed by instillation of Zenkers solution at a constant transpulmonary pressure. The left lung from each animal was used for morphometric determination of mean air space chord length (Lma). We found that the lung volume of C3 mice was substantially greater than that of B6 mice at all ages. In contrast, there was no difference in Lma (62.7 µm in C3 and 58.5 µm in B6) of 3-day-old mice. With increasing age (8 days), there was a progressive decrease in the Lma of both strains, with the magnitude of the decrease in B6 Lma mice exceeding that of C3. C3 lung volume remained 50% larger. The combination of parenchymal architectural similarity with lung air volume differences and different rates of alveolar septation support the hypothesis that lung volume and alveolar dimensions are independently regulated.
neonate; respiratory mechanics; alveolar septation; alveolar size; mean linear intercept
This article has been cited by other articles:
![]() |
U. Sajjan, S. Ganesan, A. T. Comstock, J. Shim, Q. Wang, D. R. Nagarkar, Y. Zhao, A. M. Goldsmith, J. Sonstein, M. J. Linn, et al. Elastase- and LPS-exposed mice display altered responses to rhinovirus infection Am J Physiol Lung Cell Mol Physiol, November 1, 2009; 297(5): L931 - L944. [Abstract] [Full Text] [PDF] |
||||
![]() |
G. R. Zosky, T. Z. Janosi, A. Adamicza, E. M. Bozanich, V. Cannizzaro, A. N. Larcombe, D. J. Turner, P. D. Sly, and Z. Hantos The bimodal quasi-static and dynamic elastance of the murine lung J Appl Physiol, August 1, 2008; 105(2): 685 - 692. [Abstract] [Full Text] [PDF] |
||||
![]() |
K. Ganguly, T. Stoeger, S. C. Wesselkamper, C. Reinhard, M. A. Sartor, M. Medvedovic, C. R. Tomlinson, I. Bolle, J. M. Mason, G. D. Leikauf, et al. Candidate genes controlling pulmonary function in mice: transcript profiling and predicted protein structure Physiol Genomics, November 14, 2007; 31(3): 410 - 421. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. J. Fields, J. M. Bishai, W. Mitzner, and E. M. Wagner Effects of pulmonary ischemia on lung morphology Am J Physiol Lung Cell Mol Physiol, July 1, 2007; 293(1): L254 - L258. [Abstract] [Full Text] [PDF] |
||||
![]() |
H. Fehrenbach Animal models of pulmonary emphysema: a stereologist's perspective Eur. Respir. Rev., December 1, 2006; 15(101): 136 - 147. [Abstract] [Full Text] [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| Visit Other APS Journals Online |