Loss of lung mitochondrial aconitase activity due to hyperoxia in bronchopulmonary dysplasia in primates

American Journal of Physiology - Lung Cellular and Molecular Physiology

Volumn 274, Issue 1 18-1, 1998, Pages

  Morton, Ronald L ^a   Iklé, David ^b   White, Carl W ^b  

^a NATIONAL JEWISH MEDICAL AND RESEARCH CENTER   (United States)

^b NONE

Author keywords

Baboon; Cytochrome oxidase; Oxygen; Tricarboxylic acid cycle

Indexed keywords

ACONITATE HYDRATASE;

ANIMAL EXPERIMENT; ARTICLE; BABOON; CITRIC ACID CYCLE; ENZYME ACTIVITY; HYPEROXIA; LUNG DYSPLASIA; MITOCHONDRIAL MEMBRANE; NONHUMAN; PATHOPHYSIOLOGY; PRIORITY JOURNAL;

EID: 0031931912     PISSN: 10400605     EISSN: None     Source Type: Journal    
DOI: 10.1152/ajplung.1998.274.1.l127     Document Type: Article

References (41)

1. Bassett, D. J. P., C. L. Elbon, and S. S. Reichenbaugh. Respiratory activity of lung mitochondria isolated from oxygen-exposed rats. Am. J. Physiol. 263 (Lung Cell. Mol. Physiol. 7): L439-L445, 1992.
2. Bradford, M. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal. Biochem. 72: 248-251, 1976.
3. Bruce, M. C., K. E. Wedig, N. Jentoft, R. J. Martin, P. W. Cheng, T. F. I. Boat, and A. A. Fanaroff. Altered urinary excretion of elastin cross-links in premature infants who develop bronchopulmonary dysplasia. Am. Rev. Respir. Dis. 131: 568-572, 1985.
4. Castro, L., M. Rodriguez, and R. Radi. Aconitase is readily inactivated by peroxynitrite, but not by its precursor, nitric oxide. J. Biol. Chem. 269: 29409-29415, 1994.
5. 2-mediated injury of preterm pneumocytes in vitro. Arch. Biochem. Biophys. 313: 131-138, 1994.
6. Coalson, J. J., D. R. Gerstmann, V. T. Winter, and R. A. DeLemos. Pathophysiologic, morphometric, and biochemical studies of the premature baboon with bronchopulmonary dysplasia. Am. Rev. Respir. Dis. 145: 872-881, 1992.
7. Coalson, J. J., T. J. Kuehl, M. B. Escobedo, J. L. Hilliard, F. K. M. Smith, D. M. J. Null, W. Walsh, D. Johnson, and J. L. Robotham. A baboon model of bronchopulmonary dysplasia. II. Pathologic features. Exp. Mol. Pathol. 37: 335-350, 1982.
8. Crapo, J. D., B. C. Barry, J. A. Foscue, and J. Shelburne. Structural and biochemical changes in rat lungs occurring during exposures to lethal and adaptive doses of oxygen. Am. Rev. Respir. Dis. 122: 123-143, 1980.
9. DeLemos, R. A., R. J. Roberts, J. J. Coalson, J. A. DeLemos, D. M. J. Null, and D. R. Gerstmann. Toxic effects associated with the administration of deferoxamine in the premature baboon with hyaline membrane disese. Am. J. Dis. Child. 144: 915-919, 1990.
10. Dobashi, K., K. Asayama, H. Hayashibe, A. Munim, A. Kawaoi, M. Morkawa, and S. Nakazawa. Immunohistochemical study of copper-zinc and manganese superoxide dismutases in the lungs of human fetuses and newborn infants: developmental profile and alterations in hyaline membrane disease and bronchopulmonary dysplasia. Virchows Arch. 423: 177-184, 1993.
11. Escobedo, M. B., J. L. Hilliard, F. Smith, K. Meredith, W. Walsh, D. Johnson, J. J. Coalson, T. J. Kuehl, D. M. Null, Jr., and J. L. Robotham. A baboon model of bronchopulmonary dysplasia. I. Clinical features. Exp. Mol. Pathol. 37: 323-334, 1982.
12. Flint, D. H., J. F. Tuminello, and M. H. Emptage. The inactivation of Fe-S cluster containing hydro-lyases by superoxide. J. Biol. Chem. 268: 22369-22376, 1993.
13. 2-rich environment: the antioxidant enzymes in the developing rabbit lung. Pediatr. Res. 18: 240-244, 1984.
14. Freeman, B. A., and J. D. Crapo. Hyperoxia increases oxygen radical production in rat lungs and lung mitochondria. J. Biol. Chem. 256: 10986-10992, 1981.
15. Gardner, P. R., and I. Fridovich. Superoxide sensitivity of the Escherichia coli aconitase. J. Biol. Chem. 266: 19328-19333, 1991.
16. Gardner, P. R., and I. Fridovich. Inactivation-reactivation of aconitase in Escherichia coli: a sensitive measure of superoxide radical. J. Biol. Chem. 267: 8757-8763, 1992.
17. Gardner, P. R., and I. Fridovich. Effect of glutathione on aconitase in Escherichia coli. Arch. Biochem. Biophys. 301: 98-102, 1993.
18. Gardner, P. R., D. H. Nguyen, and C. W. White. Aconitase is a sensitive and critical target of oxygen poisoning in cultured mammalian cells and in rat lungs. Proc. Natl. Acad. Sci. USA 91: 12248-12252, 1994.
19. Gardner, P. R., I. Raineri, L. B. Epstein, and C. W. White. Superoxide radical and iron modulate aconitase activity in mammalian cells. J. Biol. Chem. 270: 13399-13405, 1995.
20. Gardner, P. R., and C. W. White. Application of the aconitase method to the assay of superoxide in the mitochondrial matrices of cultures cells: effects of oxygen, redox-cycling agents, TNFα, LPS and inhibitors of respiration. In: The Oxygen Paradox, edited by K. J. A. Davies and F. Ursini. Padua, Italy: CLEUP Univ. Press, 1995, p. 33-50.
21. Gonzalez, A., I. R. Sosenko, J. Chandar, H. Hummler, N. Claure, and E. Bancalari. Influence of infection on patent ductus arteriosus and chronic lung disease in premature infants weighing 1000 grams or less. J. Pediatr. 1228: 470-478, 1996.
22. Grune, T., T. Reinheckel, M. Joshi, and K. J. Davies. Proteolysis in cultured liver epithelial cells during oxidative stress. Role of the multicatalytic proteinase complex, proteasome. J. Biol. Chem. 270: 2344-2351, 1995.
23. Haddad, I. Y., G. Pataki, P. Hu, C. Galliani, J. S. Beckman, and S. Matalon. Quantitation of nitrotyrosine levels in lung sections of patients and animals with acute lung injury. J. Clin. Invest. 94: 2407-2413, 1994.
24. Hausladen, A., and I. Fridovich. Superoxide and peroxynitrite inactivate aconitases, but nitric oxide does not. J. Biol. Chem. 269: 29405-29408, 1994.
25. Ischiropoulos, H., L. Zhu, and J. S. Beckman. Peryoxynitrite formation from macrophage-derived nitric oxide. Arch. Biochem. Biophys. 298: 446-451, 1992.
26. Kennedy, M. C., M. H. Eptage, J. Dreyer, and H. Beinert. The role of iron in the activation-reactivation of aconitase. J. Biol. Chem. 258: 11098-11115, 1983.
27. Koen, A. L., and M. Goodman. Aconitate hydratase isoenzymes: subcellular localization, tissue distribution and possible subunit structure. Biochim. Biophys. Acta 191: 698-701, 1969.
28. Kwak, E. L., D. A. Larochelle, C. Beaumont, S. V. Torti, and F. M. Torti. Role for NF-kappa B in the regulation of ferritin H by tumor necrosis factor-alpha. J. Biol. Chem. 270: 15285-15293, 1995.
29. Li, Y., T. T. Huang, E. J. Carlson, S. Melov, P. C. Ursell, J. L. Olson, L. J. Noble, M. P. Yoshimura, C. Beger, P. H. Chan, D. C. Wallace, and C. J. Epstein. Dilated cardiomyopathy and neonatal lethality in mutant mice lacking manganese superoxide dismutase. Nat. Genet. 11: 376-381, 1995.
30. Massey, V. The microestimation of succinate and the extinction coefficient of cytochrome c. Biochim. Biophys. Acta 34: 255-256, 1959.
31. Schoonen, W. G. E. J., A. H. Wanamarta, J. M. van der Klei-van Moorsel, C. Jakobs, and H. Joenje. Respiratory failure and stimulation of glycolysis in Chinese hamster ovary cells exposed to normoxic hyperoxia. J. Biol. Chem. 265: 11118-11124, 1990.
32. Seidner, S., D. McCurnin, J. J. Coalson, D. Correll, M. Leland, and R. Castro. A new model of chronic lung injury in surfactant-treated preterm baboons delivered at very early gestations (Abstract). Clin. Res. 40: 825a, 1992.
33. Smith, C. V., T. N. Hansen, N. E. Martin, H. W. McMicken, and S. J. Elliott. Oxidant stress responses in premature infants during exposure to hyperoxia. Pediatr. Res. 125: 360-365, 1993.
34. Sobonya, R. E., M. M. Logvinoff, L. M. Taussig, and A. Theriault. Morphometric analysis of the lung in prolonged bronchopulmonary dysplasia. Pediatr. Res. 16: 969-972, 1982.
35. Tanswell, A. K., and B. A. Freeman. Pulmonary antioxidant enzyme maturation in the fetal and neonatal rat. I. Developmental profiles. Pediatr. Res. 18: 584-587, 1984.
36. 2 release by lung mitochondria and microsomes. Arch. Biochem. Biophys. 217: 411-421, 1982.
37. Walther, F. J., A. B. Wade, D. Warburton, and H. J. Forman. Ontogeny of antioxidant enzymes in the fetal lamb lung. Exp. Lung Res. 17: 39-45, 1991.
38. Warshaw, J., and M. Terry. Cellular energy metabolism during fetal development. VI. Fatty acid oxidation by developing brain. Dev. Biol. 52: 161-166, 1976.
39. White, C. W., S. P. Stabler, R. H. Allen, S. Moreland, and A. A. Rosenberg. Plasma cysteine concentrations in infants with respiratory distress syndrome. J. Pediatr. 125: 769-777, 1994.
40. Williamson, J. R., and B. E. Corkey. Assays of intermediates of the citric acid cycle and related compounds by fluorometric enzyme methods. In: Methods in Enzymology, edited by J. M. Lowenstein. New York: Academic, 1969, vol. 13, p. 446-450.
41. Yam, J., L. Frank, and R. J. Roberts. Oxygen toxicity: comparison of lung biochemical responses in neonatal and adult rats. Pediatr. Res. 12: 115-118, 1978.