Effect of Peroxides on [3H]D-Aspartate Release from Bovine Isolated Retinae

Neurochemical Research

Volumn 29, Issue 4, 2004, Pages 811-818

  LeDay, Angela M ^a   Awe, Sunday O ^a   Kulkarni, Kaustubh ^b   Harris, Lydia C ^a   Opere, Catherine ^a   Dash, Alekha ^a   Ohia, Sunny E ^b  

^a CREIGHTON UNIVERSITY MEDICAL CENTER   (United States)

^b UNIVERSITY OF HOUSTON   (United States)

Author keywords

Antioxidants; Catalase; Hydrogen peroxide; Retina, aspartate release

Indexed keywords

AMITROLE; ANTIOXIDANT; ASPARTIC ACID; CATALASE; CUMENE HYDROPEROXIDE; DEXTRO ASPARTIC ACID; PEROXIDE; POTASSIUM; TROLOX C; TRITIUM;

ANIMAL TISSUE; ARTICLE; CATTLE; CONCENTRATION RESPONSE; CONTROLLED STUDY; DEPOLARIZATION; EX VIVO STUDY; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; NEUROTRANSMITTER RELEASE; NONHUMAN; OXIDATIVE STRESS; PRIORITY JOURNAL; RETINA; TISSUE LEVEL; VITREOUS BODY; ANIMAL; DRUG EFFECT; IN VITRO STUDY; METABOLISM; ORGAN CULTURE TECHNIQUE;

ANIMALIA; BOS TAURUS; BOVINAE;

ANIMALS; ASPARTIC ACID; CATTLE; CHROMATOGRAPHY, HIGH PRESSURE LIQUID; ORGAN CULTURE TECHNIQUES; PEROXIDES; RETINA; TRITIUM;

EID: 1842455060     PISSN: 03643190     EISSN: None     Source Type: Journal    
DOI: 10.1023/B:NERE.0000018855.77589.5d     Document Type: Article

References (45)

1. Martinez-Cayuela, M. 1995. Oxygen free radicals and human diseases. Biochimie 77:147-161.
2. Weigand, R., Jose, J., Rapp, L., and Anderson, R. 1984. Free radicals and damage to ocular tissues. Pages 314-353, in Armstrong, D., et al. (eds.) Free Radicals in Molecular Biology, Raven Press, New York.
3. Yamashita, H., Horie, K., Yamamota, T., Nagano, T., and Hirano, T. 1992. Light-induced retinal damage in mice: Hydrogen peroxide production and superoxide dismutase activity in retina. Retina 12:59-66.
4. Zhang, H., Agardh, E., and Agardh, C. 1991. Hydrogen peroxide production in ischaemic retina: Influence of hyperglycemia and post ischaemic oxygen tension. Diabetes Res. 6:29-35.
5. Atalla, L., Sevanian, A., and Rao, N. 1988. Hydrogen peroxide localization in ocular tissue: An electron microscopic cytochemical study. Curr. Eye Res. 7:931-936.
6. Wu, G., Gritz, D., Atalla, L., Stanford, D., Sevanian, A., and Rao, N. 1992. Ultrastructural localization of hydrogen peroxide in experimental autoimmune uveitis. Curr. Eye Res. 11:955-961.
7. Rao, N., Thaete, L., Delmage, T., and Sevanian, A. 1985. Superoxide dismutase in ocular structures. Invest. Ophthalmol. Vis. Sci. 26:1778.
8. Atalla, L., Fernandez, M., and Rao, N. 1987. Immunohistochemical localization of catalase in ocular tissue. Curr. Eye Res. 6:1181-1187.
9. Armstrong, D., Santagnelo, G., and Connole, E. 1981. The distribution of peroxide regulating enzymes in the canine eye. Curr. Eye Res. 1:225.
10. Riley, M. 1994. Physiological neutralization mechanisms and the response of the corneal endothelium to hydrogen peroxide. CLAO J. 16:1025-1033.
11. Varma, S., and Richards, R. 1988. Ascorbic acid and the eye lens. Ophthalmic Res. 20:164-173.
12. Bhuyan, K., Bhuyan, D., and Podos, S. 1986. Lipid peroxidation in cataract of the human. Life Sci. 38:1463-1471.
13. 3H]-acetylcholine release in rat cerebral synaptosomes. Neurochem. Res. 18:1047-1050.
14. Langeveld, C., Schepens, E., Stoof, J., Bast, A., Drukarch, B. 1995. Differential sensitivity to hydrogen peroxide on dopaminergic and noradrenergic neurotransmission in rat brain slices. Free Radic. Biol. Med. 19:209-217.
15. Opere, C., Tang, L., Imler, M., Kim, J., Okoye, M., and Ohia, S. 1997. Regulation of uveal sympathetic neurotransmission by peroxides. Inves. Ophthalmol. Vis. Sci. 38:842-847.
16. Rego, A., Santos, M., and Oliveira, C. 1996. Oxidative stress, hypoxia, and ischaemic-like conditions increase the release of endogenous amino acids by distinct mechanisms in cultured retinal cells. J. Neurochem. 66:2506-2516.
17. 3H]aspartate from cerebral cortical synaptosomes. J. Neurochem. 62:1757-1763.
18. 2+. J. Neurochem. 64:2552-2558.
19. 3H]D-aspartate release from bovine isolated retinae by hydrogen peroxide. Exp. Eye Res. 71:116. Abstract No. 386, S.
20. 3H]aspartate from chick retina. Eur. J. Pharmacol. 142:409-417.
21. 3H]D-aspartate release: Role in excitotoxicity. Neurochem. Res. 25: 853-860.
22. Storm-Mathisen, J. 1981. Autoradiographic and microchemical localization of high affinity glutamate uptake. Pages 89-115, in Roberts, P. J., et al. (eds.) Glutamate: Transmitter in the Central Nervous System, John Wiley & Sons, New York.
23. 3H]D-aspartate outflow from various in vitro preparations of the rat hippocampus. Neurochem. Int. 31:113-124.
24. Gandorfer, A., Putz, E., Welge-LuBen, U., Gruterich, M., Ulbig, M., and Kampik, A. 2001. Ultrastructure of the vitroretinal interface following plasmin assisted vitrectomy. Br. J. Ophthalmol. 85:6-10.
25. Ross, C. D., Parli, J. A., and Godfrey, D. A. 1989. Quantitative distribution of six amino acid in rat retinal layers. Vis. Res. 29:1079-1084.
26. Pryor, W. A. 1976. The role of free radical reactions in biological systems. Pages 1-49, in Free Radicals in Biology, Vol. 1 Academic Press, New York.
27. Penn, J., Tolman, B., and Bullard, L. 1997. Effect of a water-soluble vitamin E analog, trolox C, on retinal vascular development in an animal model of retinopathy of prematurity. Free Radic. Biol. Med. 22:977-984.
28. 3H]D-aspartate from cultured chick retinal cells. Neurochem. Res. 21:361-368.
29. 2+ sensitivity of the exocytosis of glutamate in cerebrocortical synaptosomes. Biochem. Biophys. Res. Commun. 219:198-204.
30. Opere, C. A., and Ohia, S. E. 1998. Role of intracellular calcium in peroxide-induced potentiation of norepinephrine release from bovine isolated irides. Gen. Pharmacol. 31:793-78.
31. Opere, C. A., Opere, D., and Ohia, S. E. 1998. Mechanism of peroxide-induced potentiation of sympathetic neurotransmission in bovine irides: Role of extracellular calcium. Free Radic. Res. 28:283-292.
32. Taguchi, H., Ogura, Y., Takanishi, T., Hashizoe, M., and Honda, Y. 1996. In vivo quantitation of peroxides in the vitreous humor by fluorophotometry. Inves. Ophthalmol. Vis. Sci. 37:1444-1450.
33. Cao, W., Tobran-Tink, J., Chen, W., Mrazek, D., Elias, R., and McGinnis, J. F. 1999. Pigment epithelium-derived factor protects cultured retinal neurons against hydrogen peroxide-induced cell death. Neurosci. Res. 57:789-800.
34. Doba, T., Burton, G., and Ingold, K. 1985. Antioxidant and coantioxidant activity of vitamin C: The effect of vitamin C, either alone or in the presence of vitamin E or a water-soluble vitamin E analogue, upon the peroxidation of aqueous multilamellar phospholipid liposomes. Biochim. Biophys. Acta 835: 298-303.
35. Suttorp, N., Toepfer, W., and Roka, L. 1986. Antioxidant defense mechanisms of endothelial cells: glutathione redox cycle versus catalase. Am. J. Physiol. 251:C671-C680.
36. Le, C. T., Hollaar, L., Van-der-Valk, E. J., Franken, N. A., Van Ravels, F. J., Wondergem, J., and Van der Laase, A. 1995. Protection of myocytes against free radical-induced damage by accelerated turnover of the glutathione redox cycle. Eur. Heart J. 16:553-562.
37. Ueda, J., Saito, N., and Ozawa, T. 1996. Detection of free radicals produced from the reactions of lipid hydroperoxide model compounds with Cu(II) complexes by ESR spectroscopy. Arch. Biochem. Biophys. 325:65-76.
38. Takanashi, H., Ogura, Y., Taguchi, H., Hashizoe, M., and Honda, Y. 1997. Flurophotometric quantitation of oxidative stress in the retina in vivo. Invest. Ophthalmol. Vis. Sci. 38:2721-2728.
39. Matutte, B., Awe, S., Ameh, F., LeDay, A., Rice, J. C., Opere, C., and Ohia, S. E. 2000. Role of catalase in pre- and postjunctional responses of mammalian irides to hydrogen peroxide. J. Ocul. Pharmacol. Ther. 16:429-438.
40. 2 by the mouse lens. Exp. Eye Res. 64:477-485.
41. Costarides, A., Recasens, J. F., Riley, M. V., and Green, K. 1989. The effects of ascorbate, 3-aminotriazole, and 1,3-bis-(2-chloroethyl) -1-nitrosourea on hydrogen peroxide levels in the rabbit aqueous humor. Lens Eye Tox. Res. 6:167-173.
42. Ohta, Y., Yamasaki, T., Niwa, T., Niimi, K., Majima, Y., and Ishiguro, L. 1996. Role of catalase in retinal antioxidant defence system: Its comparative study among rabbits, guinea pigs, and rats. Ophthalmic Res. 28:336-342.
43. Delamere, N., and Williams. R. 1985. Detoxification of hydrogen peroxide by the rabbit iris-ciliary body. Exp. Eye Res. 40:805-811.
44. Vorwerk, C., Gorla, M., and Dreyer, E. 1999. An experimental basis for implicating excitotoxicity in glaucomatous optic neuropathy. Surv. Ophthalmol. 43 (Suppl. 1):S142-S150.
45. +-ATPase in brain vesicles at micromolar concentrations. J. Neurochem. 70:646-652.