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Proceedings of the National Academy of Sciences of the United States of America logoLink to Proceedings of the National Academy of Sciences of the United States of America
. 1995 Feb 14;92(4):1105–1107. doi: 10.1073/pnas.92.4.1105

Sexual dimorphism in the architecture of the lung's gas-exchange region.

G D Massaro 1, J P Mortola 1, D Massaro 1
PMCID: PMC42646  PMID: 7862643

Abstract

The lung's only vital function is to provide sufficient gas-exchange surface area (Sa) to meet the organism's needs for oxygen uptake (VO2) and carbon dioxide elimination. A direct linear relation between Sa and VO2 and an inverse linear relation between the size of the lung's gas-exchange units and the species mass-specific VO2 are strongly conserved across species. Within species, Sa increases in response to prolonged (weeks) elevation of VO2. We now report sex-dependent deviations from these relationships that seem to anticipate the need for increased gas-exchange capacity engendered in females by the metabolic demands of pregnancy and lactation. We found that although VO2 almost doubled in rats during pregnancy and lactation, Sa was the same in age-matched virgin, pregnant, and lactating females. However, at the onset of sexual maturity, virgin female rats and mice had higher mass-specific Sa than males of the same species although mass-specific VO2 was identical, within species, in both sexes. In addition, even though mass-specific VO2 was identical in males and females, alveoli were 30% and 50% smaller in female rats and mice, respectively, than males of the same species. We suggest the greater mass-specific Sa and smaller alveoli in females in spite of identical mass-specific VO2 as males were selected for evolutionarily; they help females meet the metabolic demands of reproduction without adding to the energy demands of these periods a requirement to form additional lung.

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Selected References

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  1. Callas G., Adkisson V. T. The effects of desiccated thyroid on the rat lung. Anat Rec. 1980 Jul;197(3):331–337. doi: 10.1002/ar.1091970307. [DOI] [PubMed] [Google Scholar]
  2. Cruz-Orive L. M. Particle number can be estimated using a disector of unknown thickness: the selector. J Microsc. 1987 Feb;145(Pt 2):121–142. [PubMed] [Google Scholar]
  3. Cruz-Orive L. M., Weibel E. R. Sampling designs for stereology. J Microsc. 1981 Jun;122(Pt 3):235–257. doi: 10.1111/j.1365-2818.1981.tb01265.x. [DOI] [PubMed] [Google Scholar]
  4. Diamond J., Hammond K. The matches, achieved by natural selection, between biological capacities and their natural loads. Experientia. 1992 Jun 15;48(6):551–557. doi: 10.1007/BF01920238. [DOI] [PubMed] [Google Scholar]
  5. Frappell P., Saiki C., Mortola J. P. Metabolism during normoxia, hypoxia and recovery in the newborn kitten. Respir Physiol. 1991 Oct;86(1):115–124. doi: 10.1016/0034-5687(91)90043-i. [DOI] [PubMed] [Google Scholar]
  6. Gehr P., Mwangi D. K., Ammann A., Maloiy G. M., Taylor C. R., Weibel E. R. Design of the mammalian respiratory system. V. Scaling morphometric pulmonary diffusing capacity to body mass: wild and domestic mammals. Respir Physiol. 1981 Apr;44(1):61–86. doi: 10.1016/0034-5687(81)90077-3. [DOI] [PubMed] [Google Scholar]
  7. Gundersen H. J., Jensen E. B. Stereological estimation of the volume-weighted mean volume of arbitrary particles observed on random sections. J Microsc. 1985 May;138(Pt 2):127–142. doi: 10.1111/j.1365-2818.1985.tb02607.x. [DOI] [PubMed] [Google Scholar]
  8. Hugonnaud C., Gehr P., Weibel R., Burri P. H. Adaptation of the growing lung to increased oxygen consumption. II. Morphometric analysis. Respir Physiol. 1977 Feb;29(1):1–10. doi: 10.1016/0034-5687(77)90112-8. [DOI] [PubMed] [Google Scholar]
  9. Lechner A. J., Banchero N. Lung morphometry in guinea pigs acclimated to cold during growth. J Appl Physiol Respir Environ Exerc Physiol. 1980 May;48(5):886–891. doi: 10.1152/jappl.1980.48.5.886. [DOI] [PubMed] [Google Scholar]
  10. Massaro G. D., Massaro D. Formation of alveoli in rats: postnatal effect of prenatal dexamethasone. Am J Physiol. 1992 Jul;263(1 Pt 1):L37–L41. doi: 10.1152/ajplung.1992.263.1.L37. [DOI] [PubMed] [Google Scholar]
  11. TENNEY S. M., REMMERS J. E. Comparative quantitative morphology of the mammalian lung: diffusing area. Nature. 1963 Jan 5;197:54–56. doi: 10.1038/197054a0. [DOI] [PubMed] [Google Scholar]
  12. Thompson M. E. Lung growth in response to altered metabolic demand in hamsters: influence of thyroid function and cold exposure. Respir Physiol. 1980 Jun;40(3):335–347. doi: 10.1016/0034-5687(80)90033-x. [DOI] [PubMed] [Google Scholar]

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