Skip to main content
The American Journal of Pathology logoLink to The American Journal of Pathology
. 1985 Aug;120(2):244–247.

Ascorbate in aqueous humor protects against myeloperoxidase-induced oxidation.

J T Rosenbaum, E L Howes Jr, D English
PMCID: PMC1887821  PMID: 2992283

Abstract

Chemotactic factors can cause polymorphonuclear leukocytes to release the contents of azurophilic granules, including the enzymes beta-glucuronidase and myeloperoxidase. In the presence of aqueous humor from the anterior chamber of the rabbit eye, the supernatant from stimulated leukocytes contains beta-glucuronidase, but myeloperoxidase is not detectable. Studies with aqueous humor and partially purified human myeloperoxidase suggest that this phenomenon is not due to a failure of enzyme release. The factor responsible for the inability to detect MPO in the assay system is heat-labile, dialyzable, and reversed by ascorbate oxidase. Comparable assay inhibition is produced by ascorbic acid at a concentration present in either human or rabbit aqueous humor. The ability of aqueous humor to protect against myeloperoxidase-induced oxidation may contribute to several diverse phenomena, including the susceptibility of the eye to Candida infection and a prolonged half-life for several inflammatory mediators in the anterior chamber.

Full text

PDF
244

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Bainton D. F., Farquhar M. G. Differences in enzyme content of azurophil and specific granules of polymorphonuclear leukocytes. II. Cytochemistry and electron microscopy of bone marrow cells. J Cell Biol. 1968 Nov;39(2):299–317. doi: 10.1083/jcb.39.2.299. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Bito L. Z. The effects of experimental uveitis on anterior uveal prostaglandin transport and aqueous humor composition. Invest Ophthalmol. 1974 Dec;13(12):959–966. [PubMed] [Google Scholar]
  3. Brittinger G., Hirschhorn R., Douglas S. D., Weissmann G. Studies on lysosomes. XI. Characterization of a hydrolase-rich fraction from human lymphocytes. J Cell Biol. 1968 May;37(2):394–411. doi: 10.1083/jcb.37.2.394. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Cech P., Papathanassiou A., Boreux G., Roth P., Miescher P. A. Hereditary myeloperoxidase deficiency. Blood. 1979 Mar;53(3):403–411. [PubMed] [Google Scholar]
  5. Clark R. A., Szot S. Chemotactic factor inactivation by stimulated human neutrophils mediated by myeloperoxidase-catalyzed methionine oxidation. J Immunol. 1982 Apr;128(4):1507–1513. [PubMed] [Google Scholar]
  6. Drath D. B., Karnovsky M. L. Bactericidal activity of metal-mediated peroxide-ascorbate systems. Infect Immun. 1974 Nov;10(5):1077–1083. doi: 10.1128/iai.10.5.1077-1083.1974. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Edwards J. E., Jr, Foos R. Y., Montgomerie J. Z., Guze L. B. Ocular manifestations of Candida septicemia: review of seventy-six cases of hematogenous Candida endophthalmitis. Medicine (Baltimore) 1974 Jan;53(1):47–75. doi: 10.1097/00005792-197401000-00002. [DOI] [PubMed] [Google Scholar]
  8. El-Maallem H., Fletcher J. Impaired neutrophil function and myeloperoxidase deficiency in myeloid metaplasia. Br J Haematol. 1977 Nov;37(3):323–329. doi: 10.1111/j.1365-2141.1977.tb01002.x. [DOI] [PubMed] [Google Scholar]
  9. Henson P. M., Zanolari B., Schwartzman N. A., Hong S. R. Intracellular control of human neutrophil secretion. I. C5a-induced stimulus-specific desensitization and the effects of cytochalasin B. J Immunol. 1978 Sep;121(3):851–855. [PubMed] [Google Scholar]
  10. Lee C. W., Lewis R. A., Tauber A. I., Mehrotra M., Corey E. J., Austen K. F. The myeloperoxidase-dependent metabolism of leukotrienes C4, D4, and E4 to 6-trans-leukotriene B4 diastereoisomers and the subclass-specific S-diastereoisomeric sulfoxides. J Biol Chem. 1983 Dec 25;258(24):15004–15010. [PubMed] [Google Scholar]
  11. Lehrer R. I., Cline M. J. Leukocyte myeloperoxidase deficiency and disseminated candidiasis: the role of myeloperoxidase in resistance to Candida infection. J Clin Invest. 1969 Aug;48(8):1478–1488. doi: 10.1172/JCI106114. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Matheson N. R., Wong P. S., Schuyler M., Travis J. Interaction of human alpha-1-proteinase inhibitor with neutrophil myeloperoxidase. Biochemistry. 1981 Jan 20;20(2):331–336. doi: 10.1021/bi00505a016. [DOI] [PubMed] [Google Scholar]
  13. Olsson I., Venge P. Cationic proteins of human granulocytes. II. Separation of the cationic proteins of the granules of leukemic myeloid cells. Blood. 1974 Aug;44(2):235–246. [PubMed] [Google Scholar]
  14. Paredes J. M., Weiss S. J. Human neutrophils transform prostaglandins by a myeloperoxidase-dependent mechanism. J Biol Chem. 1982 Mar 25;257(6):2738–2740. [PubMed] [Google Scholar]
  15. Rosenbaum J. T., Wong K., Perez H. D., Raymond W., Howes E. L., Jr Characterization of endotoxin-induced C5-derived chemotactic activity in aqueous humor. Invest Ophthalmol Vis Sci. 1984 Oct;25(10):1184–1191. [PubMed] [Google Scholar]
  16. Simmons S. R., Karnovsky M. L. Iodinating ability of various leukocytes and their bactericidal activity. J Exp Med. 1973 Jul 1;138(1):44–63. doi: 10.1084/jem.138.1.44. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Spector R. Vitamin homeostasis in the central nervous system. N Engl J Med. 1977 Jun 16;296(24):1393–1398. doi: 10.1056/NEJM197706162962409. [DOI] [PubMed] [Google Scholar]
  18. Varma S. D., Srivastava V. K., Richards R. D. Photoperoxidation in lens and cataract formation: preventive role of superoxide dismutase, catalase and vitamin C. Ophthalmic Res. 1982;14(3):167–175. doi: 10.1159/000265189. [DOI] [PubMed] [Google Scholar]
  19. White-Stevens R. H. Interference by ascorbic acid in test systems involving peroxidase. I. Reversible indicators and the effects of copper, iron, and mercury. Clin Chem. 1982 Apr;28(4 Pt 1):578–588. [PubMed] [Google Scholar]
  20. van Heuven W. A., Lam K. W., Ray G. S. Source of subretinal fluid on the basis of ascorbate analyses. Arch Ophthalmol. 1982 Jun;100(6):976–978. doi: 10.1001/archopht.1982.01030030984017. [DOI] [PubMed] [Google Scholar]

Articles from The American Journal of Pathology are provided here courtesy of American Society for Investigative Pathology

RESOURCES