Progressive deterioration of pulmonary mechanics during aging has been documented repeatedly. Biochemical aspects of aging in the lung have received much less attention, and in particular, pulmonary bioenergetics have not been investigated at all. Bioenergetics in the aging lung are of immense importance to cellular viability and longevity, and hence, to maintenance of proper organ function and resistance to disease and injury. This project will examine the hypothesis that the aged lung has a decreased capacity for bioenergetic metabolism compared to the adult organ. Specifically, the pulmonary epithelium will be the focus of investigation. This lung surface is the site of gas exchange and as such, is the initial site for many types of pulmonary injury. The hypothesis predicts that the epithelial cells in aged lungs will respond less efficiently to injury. To investigate this, a reproducible model of oxidant lung injury has been developed using acute exposure (8 hours) to three concentrations of ozone. In this model, specific and separate phases of epithelial injury, cellular proliferation and recovery have been defined. Each of these phases may be ovserved during graded levels of injury defined as mild, moderate and severe by the extent of epithelial damage. To fully evaluate the bioenergetic consequences of this typical oxidant injury, both mitochondrial and cytoplasmic bioenergetic metabolism will be investigated. Also, the cellular consequences of this injury, both in adult and aged animals, will be quantitated in terms of lipid and protein damage and defensive responses. All biochemical studies will be correlated with the morphoetric alterations appearing both in the whole organ and in isolated Type II pulmonary epithelium. These combined studies will provide the first information on the effects of aging on pulmonary bioenergetics in the noral, healthy mammal and during the situation of lung injury from a chemical that is typical of numerous common pulmonary toxins.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Research Project (R01)
Project #
5R01AG007801-02
Application #
3119130
Study Section
Toxicology Study Section (TOX)
Project Start
1988-08-01
Project End
1993-07-31
Budget Start
1989-08-01
Budget End
1990-07-31
Support Year
2
Fiscal Year
1989
Total Cost
Indirect Cost
Name
University of South Florida
Department
Type
Schools of Public Health
DUNS #
City
Tampa
State
FL
Country
United States
Zip Code
33612
Byvoet, P; Balis, J U; Shelley, S A et al. (1995) Detection of hydroxyl radicals upon interaction of ozone with aqueous media or extracellular surfactant: the role of trace iron. Arch Biochem Biophys 319:464-9
Vesely, D L; Giordano, A T; Raska-Emery, P et al. (1994) Increase in atrial natriuretic factor in the lungs, heart, and circulatory system owing to ozone. Chest 105:1551-4
Vesely, D L; Giordano, A T; Raska-Emery, P et al. (1994) Ozone increases atrial natriuretic peptides in heart, lung and circulation of aged vs. adult animals. Gerontology 40:227-36
Vesely, D L; Giordano, A T; Raska-Emery, P et al. (1994) Ozone increases amino- and carboxy-terminal atrial natriuretic factor prohormone peptides in lung, heart, and circulation. J Biochem Toxicol 9:107-12
Giordano, A T; Raska-Emery, P; Montgomery, M R et al. (1993) Increased atrial natriuretic factor prohormone peptides with aging in the heart, but not in lung, liver, or intestine. Growth Dev Aging 57:111-20
Paterson, J F; Hammond, M D; Montgomery, M R et al. (1992) Acute ozone-induced lung injury in rats: structural-functional relationships of developing alveolar edema. Toxicol Appl Pharmacol 117:37-45
Haller, E M; Shelley, S A; Montgomery, M R et al. (1992) Immunocytochemical localization of lysozyme and surfactant protein A in rat type II cells and extracellular surfactant forms. J Histochem Cytochem 40:1491-500
Montgomery, M R; Raska-Emery, P; Balis, J U (1991) Recovery of lung pyridine nucleotides following acute exposure of adult and aged rats to ozone. J Toxicol Environ Health 34:115-26
Balis, J U; Paterson, J F; Lundh, J M et al. (1991) Ozone stress initiates acute perturbations of secreted surfactant membranes. Am J Pathol 138:847-57
Zychlinski, L; Raska-Emery, P; Balis, J U et al. (1989) Age-related difference in bioenergetics of lung and heart mitochondrial from rats exposed to ozone. J Biochem Toxicol 4:251-4

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