Influence of intense sound exposure on glutathione synthesis in the cochlea

Brain Research

Volumn 804, Issue 1, 1998, Pages 72-78

  Yamasoba, Tatsuya ^a,b   Harris, Craig ^c   Shoji, Fumi ^a   Lee, Rosanna J ^c   Nuttall, Alfred L ^a,d   Miller, Josef M ^a  

^a UNIVERSITY OF MICHIGAN HEALTH SYSTEM   (United States)

^b UNIVERSITY OF TOKYO   (Japan)

^c UNIVERSITY OF MICHIGAN   (United States)

^d OREGON HEALTH AND SCIENCE UNIVERSITY   (United States)

Author keywords

Acoustic trauma; Cochlea; Guinea pig; High performance liquid chromatography; Noise induced hearing loss; Reactive oxygen species

Indexed keywords

CYSTEINE; GLUTATHIONE;

ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; COCHLEA; CONTROLLED STUDY; FEMALE; GUINEA PIG; HEARING LOSS; NEUROEPITHELIUM; NOISE; NONHUMAN; PRIORITY JOURNAL;

ANIMALS; CHROMATOGRAPHY, HIGH PRESSURE LIQUID; COCHLEA; CYSTEINE; FEMALE; GLUTATHIONE; GUINEA PIGS; NOISE; TISSUE DISTRIBUTION;

EID: 0032584953     PISSN: 00068993     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0006-8993(98)00660-X     Document Type: Article

References (28)

1. T.M.E. Anderson, M. Underwood, R.J. Bridges, A. Meister, Glutathione metabolism at the blood-cerebrospinal fluid barrier, FASEB J. 3 (1989) 2527-2531.
2. R.P. Bobbin, M. Fallon, Intense sound increases the level of an unidentified amine found in perilymph, Hear. Res. 63 (1992) 157-162.
3. R.P. Bobbin, M. Fallon, C. LeBlanc, A. Baber, Evidence that glutathione is the unidentified amine (Unk 2.5) released by high potassium into cochlear fluids, Hear. Res. 87 (1995) 49-54.
4. B. Chance, H. Sies, A. Boveris, Hydroperoxide metabolism in mammalian organs, Physiol. Rev. 59 (1979) 527-605.
5. R.W. D'Souza, W.R. Francis, M.E. Andersen, Physiological model for tissue glutathione depletion and increased resynthesis after ethylene dichloride exposure, J. Pharmacol. Exp. Ther. 245 (1988) 563-568.
6. A. El Barbary, R. Altschuler, J. Schacht, Glutathione S-transferases in the organ of Corti of the rat: enzymatic activity, subunit composition and immunohistological localization, Hear. Res. 71 (1993) 80-90.
7. H. Esterbauer, R.J. Schaur, H. Zollner, Chemistry and biochemistry of 4-hydroxynonenal, malonaldehyde and related aldehydes, Free Radic. Biol. Med. 11 (1991) 81-128.
8. O.W. Griffith, A. Meister, Glutathione: interorgan translocation, turnover and metabolism, Proc. Natl. Acad. Sci. U.S.A. 76 (1979) 5606-5610.
9. C. Harris, Glutathione biosynthesis in the postimplantation rat conceptus in vitro, Toxicol. Appl. Pharmacol. 120 (1993) 247-256.
10. C. Harris, M.J. Namkung, M.R. Juchau, Regulation of intracellular glutathione in rat embryos and visceral yolk sacs and its effect on 2-nitrosofluorene-induced malformations in the whole embryo culture system, Toxicol. Appl. Pharmacol. 88 (1987) 141-152.
11. D.W. Hoffman, C.A. Whitworth, K.L. Jones, L.P. Rybak, Nutritional status, glutathione levels, and ototoxicity of loop diuretics and aminoglycoside antibiotics, Hear. Res. 31 (1987) 217-222.
12. D.W. Hoffman, C.A. Whitworth, K.L. Jones-King, L.P. Rybak, Potentiation of ototoxicity by glutathione depletion, Ann. Otol. Rhinol. Laryngol. 97 (1988) 36-41.
13. B.H. Hu, X.Y. Zheng, S.L. McFadden, R.D. Kopke, D. Henderson, R-phenylisopropyladenosine attenuates noise-induced hearing loss in the chinchilla, Hear. Res. 113 (1997) 198-206.
14. A.A. Jacono, B. Hu, R.D. Kopke, D. Henderson, T.R. Van de Water, H.M. Steinman, Changes in cochlear antioxidant enzyme activity after sound conditioning and noise exposure in the chinchilla, Hear. Res. 117 (1998) 31-38.
15. I. Kruman, A.J. Bruce-Keller, D. Bredsen, G. Waeg, M.P. Mattson, Evidence that 4-hydroxynonenal mediates oxidative stress-induced neuronal apoptosis, J. Neurosci. 17 (1997) 5089-5100.
16. J. Lautermann, S.A. Crann, J. McLaren, J. Schacht, Glutathione-dependent antioxidant systems in the mammalian inner ear: effects of aging, ototoxic drugs and noise, Hear. Res. 114 (1997) 75-82.
17. J. Lautermann, J. McLaren, J. Schacht, Glutathione protection against gentamicin ototoxicity depends on nutritional status, Hear. Res. 86 (1995) 15-24.
18. J. Lautermann, B. Song, J. McLaren, J. Schacht, Diet is a risk factor in cisplatin ototoxicity, Hear. Res. 88 (1995) 47-53.
19. M.P. Mattson, Modification of ion homeostasis by lipid peroxidation: roles in neuronal degeneration and adaptive plasticity, Trends Neurosci. 20 (1998) 53-57.
20. A. Meister, M.E. Anderson, Glutathione, Annu. Rev. Biochem. 52 (1983) 711-760.
21. K.K. Ohlemiller, L.L. Dugan, In vivo measurement of cochlear reactive oxygen species (ROS) in mice: effects of noise exposure and cochlear ischemia, Assoc. Res. Otolaryngol. Abstr. 21 (1998) 518.
22. S. Orrenius, P. Moldéus, The multiple roles of glutathione in drug metabolism, Trends Pharmacol. Sci. 6 (1984) 432-435.
23. W.S. Quirk, B.G. Shivapuja, C.L. Schwimmer, M.D. Seidman, Lipid peroxidation inhibitor attenuates noise-induced temporary threshold shifts, Hear. Res. 74 (1994) 217-220.
24. R. Ravi, S.M. Somani, L.P. Rybak, Mechanism of cisplatin ototoxicity: antioxidant system, Pharmacol. Toxicol. 76 (1995) 386-394.
25. M.D. Seidman, B.G. Shivapuja, W.S. Quirk, The protective effects of allopurinol and superoxide dismutase on noise-induced cochlear damage, Otolaryngol. Head Neck Surg. 109 (1993) 1052-1056.
26. S. Usami, O.P. Hjelle, O.P. Ottersen, Differential cellular distribution of glutathione, an endogenous antioxidant, in the guinea pig inner ear, Brain Res. 743 (1996) 337-340.
27. H. Yamane, Y. Nakai, M. Takayama, H. Iguchi, T. Nakagawa, A. Kojima, Appearance of free radicals in the guinea pig inner ear after noise-induced acoustic trauma, Arch. Otorhinolaryngol. 252 (1995) 504-508.
28. T. Yamasoba, A.L. Nuttall, C. Harris, Y. Raphael, J.M. Miller, Role of glutathione in protection against noise-induced hearing loss, Brain Res. 784 (1998) 82-90.