Cochlear injuries induced by the combined exposure to noise and styrene

Hearing Research

Volumn 254, Issue 1-2, 2009, Pages 25-33

  Chen, Guang Di ^a   Henderson, Donald ^a  

^a UNIVERSITY AT BUFFALO   (United States)

Author keywords

Cochlear injury; Noise and chemical interaction; Noise trauma; Styrene ototoxicity

Indexed keywords

STYRENE;

ANIMAL EXPERIMENT; ANIMAL MODEL; APOPTOSIS; ARTICLE; AUDITORY THRESHOLD; CELL DEATH; COCHLEA; CONTROLLED STUDY; ENVIRONMENTAL EXPOSURE; HAIR CELL; INNER EAR DISEASE; MAGNOCELLULAR NUCLEUS; MALE; NOISE; NOISE INJURY; NONHUMAN; PRIORITY JOURNAL; RAT; STRESS;

ACTION POTENTIALS; ANIMALS; APOPTOSIS; CELL DEATH; CELL NUCLEUS; COCHLEA; HAIR CELLS, AUDITORY; HEARING LOSS, NOISE-INDUCED; MALE; NOISE; RATS; RATS, LONG-EVANS; STYRENE; SUCCINATE DEHYDROGENASE; TIME FACTORS;

EID: 67649502903     PISSN: 03785955     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.heares.2009.04.005     Document Type: Article

References (49)

1. Barregard L., and Axelsson A. Is there an ototraumatic interaction between noise and solvents?. Scand. Audiol. 13 (1984) 151-155
2. Calabrese G., Martini A., Sessa G., Cellini M., Bartolucci G.B., Marcuzzo G., and De Rosa E. Otoneurological study of workers exposed to styrene in the fiberglass industry. Int. Arch. Occup. Environ. Health. 68 (1996) 219-223
3. Campo P., Loquet G., Blachere V., and Roure M. Toluene and styrene intoxication route in the rat cochlea. Neurotoxicol. Teratol. 21 (1999) 427-434
4. Campo P., Lataye R., Loquet G., and Bonnet P. Styrene-induced hearing loss: a membrane insult. Hear. Res. 154 (2001) 170-180
5. Chen G.D. Prestin gene expression in the rat cochlea following intense noise exposure. Hear. Res. 222 (2006) 54-61
6. Chen G.D., and Fechter L.D. The relationship between noise-induced hearing loss and hair cell loss in rats. Hear. Res. 177 (2003) 81-90
7. Chen G.D., and Zhao H.B. Effects of intense noise exposure on the outer hair cell plasma membrane fluidity. Hear. Res. 226 (2007) 14-21
8. Chen G.D., Chi L.H., Kostyniak P.J., and Henderson D. Styrene induced alterations in biomarkers of exposure and effects in the cochlea: mechanisms of hearing loss. Toxicol. Sci. 98 (2007) 167-177
9. Chen G.D., Tanaka C., and Henderson D. Relationship between outer hair cell loss and hearing loss in rats exposed to styrene. Hear. Res. 243 (2008) 28-34
10. Fechter L.D. Effects of acute styrene and simultaneous noise exposure on auditory function in the guinea pig. Neurotoxicol. Teratol. 15 (1993) 151-155
11. Gagnaire F., and Langlais C. Relative ototoxicity of 21 aromatic solvents. Arch. Toxicol. 79 (2005) 346-354
12. Henderson D., Spongr V., Subramaniam M., and Campo P. Anatomical effects of impact noise. Hear. Res. 76 (1994) 101-117
13. Henderson D., McFadden S.L., Liu C.C., Hight N., and Zheng X.Y. The role of antioxidants in protection from impulse noise. Ann. NY Acad. Sci. 884 (1999) 368-380
14. Jacobsen P., Hein H.O., Suadicani P., Parving A., and Gyntelberg F. Mixed solvent exposure and hearing impairment: an epidemiological study of 3284 men. The Copenhagen male study. Occup. Med. 43 (1993) 180-184
15. Johnson A.C., Juntunen L., Nylen P., Borg E., and Hoglund G. Effect of interaction between noise and toluene on auditory function in the rat. Acta Otolaryngol. (Stockh.) 105 (1988) 56-63
16. Johnson A.C., and Nylén P.R. Effects of industrial solvents on hearing. Occup. Med. 10 (1995) 623-640
17. Kopke R.D., Weisskopf P.A., Boone J.L., Jackson R.L., Wester D.C., Hoffer M.E., Lambert D.C., Charon C.C., Ding D.L., and McBride D. Reduction of noise-induced hearing loss using L-NAC and salicylate in the chinchilla. Hear. Res. 149 (2000) 138-146
18. Koskinen M., Vodicka P., and Hemminki K. Identification of 1-adenine DNA adducts in workers occupationally exposed to styrene. Occup. Environ. Med. 43 (2001) 694-700
19. Koskinen M., Vodickova L., Vodicka P., Warner S., and Hemminki K. Kinetics of formation of specific styrene oxide adducts in double-stranded DNA. Chem. Biol. Interact. 138 (2001) 111-124
20. Lataye R., and Campo P. Combined e¡ects of a simultaneous exposure to noise and toluene on hearing function. Neurotoxicol. Teratol. 19 (1997) 373-382
21. Lataye R., Campo P., and Loquet G. Combined effects of noise and styrene exposure on hearing function in the rat. Hear. Res. 139 (2000) 86-96
22. Lataye R., Campo P., Barthelemy C., Loquet G., and Bonnet P. Cochlear pathology induced by styrene. Neurotoxicol. Teratol. 23 (2001) 71-79
23. Lataye R., Campo P., Pouyatos B., Cossec B., Blachere V., and Morel G. Solvent ototoxicity in the rat and guinea pig. Neurotoxicol. Teratol. 25 (2003) 39-50
24. Liu Z. Experimental study on the mechanism of free radical in blast trauma induced hearing loss. Chung Hua Erh Pi Yen Hou Ko Tsa Chih. 27 (1992) 24-26
25. Liu S.F., Fang Q.M., Jin Z.L., and Rappaport M.S. Investigation of protein-styrene oxide adducts as a molecular biomarker of human exposed to styrene. J. Environ. Sci. (China) 13 (2001) 391-397
26. Loquet G., Campo P., and Lataye R. Comparison of toluene-induced and styrene-induced hearing losses. Neurotoxicol. Teratol. 21 (1999) 689-697
27. Loquet G., Campo P., Lataye R., Cossec B., and Bonnet P. Combined effects of exposure to styrene and ethanol on the auditory function in the rat. Hear. Res. 148 (2000) 173-180
28. Makitie A., Pirvola U., Pyykko I., Sakakibara H., Riihimaki V., and Ylikoski J. The ototoxic interaction of styrene and noise. Hear. Res. 179 (2003) 9-20
29. Marczynski B., Peel M., and Baur X. New aspects in genotoxic risk assessment of styrene exposure-a working hypothesis. Med. Hypotheses 54 (2000) 619-623
30. Miller R.R., Newhook R., and Poole A. Styrene production, use, and human exposure. Crit. Rev. Toxicol. 24 Suppl. 1 (1994) S1-S10
31. Mizunuma K., Yasugi T., Kawai T., Horiguchi S., and Ikeda M. Exposure-excretion relationship of styrene and acetone in factory workers: a comparison of a lipophilic solvent and a hydrophilic solvent. Arch. Environ. Contam. Toxicol. 25 (1993) 129-133
32. Möller C., Odkvist L., Larsby B., Tham R., Ledin T., and Bergholtz L. Otoneurological findings in workers exposed to styrene. Scand. J. Work. Environ. Health. 16 (1990) 189-194
33. Morata T.C., Dunn D.E., and Sieber W.K. Occupational exposure to noise and ototoxic organic solvents. Arch. Environ. Health 49 (1994) 359-365
34. Morata T.C., Johnson A.C., Nylen P., Svensson E.B., Cheng J., Krieg E.F., Lindblad A.C., Ernstgard L., and Franks J. Audiometric findings in workers exposed to low levels of styrene and noise. J. Occup. Environ. Med. 44 (2002) 806-814
35. Morioka I., Kuroda M., Miyashita K., and Takeda S. Evaluation of organic solvent ototoxicity by the upper limit of hearing. Arch. Environ. Health. 54 (1999) 341-346
36. Muijser H., Hoogendijk E.M.G., and Hooisma J. The effects of occupational exposure to styrene on high-frequency hearing thresholds. Toxicology 49 (1988) 331-340
37. Ohinata Y., Miller J.M., Altschuler R.A., and Schacht J. Intense noise induces formation of vasoactive lipid peroxidation products in the cochlea. Brain Res. 878 (2000) 163-173
38. Ohlemiller K.K., Wright J.S., and Dugan L.L. Early elevation of cochlear reactive oxygen species following noise exposure. Audiol. Neurootol. 4 (1999) 229-236
39. Ohlemiller K.K., McFadden S.L., Ding D.L., Flood D.G., Reaume A.G., Hoffman E.K., Scott R.W., Wright J.S., Putcha G.V., and Salvi R.J. Targeted deletion of the cytosolic Cu/Zn-superoxide dismutase gene (Sod1) increases susceptibility to noise-induced hearing loss. Audiol. Neurootol. 4 (1999) 237-246
40. Rao D., and Fechter L.D. Protective effects of phenyl-N-tert-butylnitrone on the potentiation of noise-induced hearing loss by carbon monoxide. Toxicol. Appl. Pharmacol. 167 2 (2000) 125-131
41. Rao D.B., Moore D.R., Reinke L.A., and Fechter L.D. Free radical generation in the cochlea during combined exposure to noise and carbon monoxide: an electrophysiological and an EPR study. Hear. Res. 161 (2001) 113-122
42. Rybak L.P. Hearing: the effects of chemicals. Otolaryngol. Head. Neck. Surg. 106 (1992) 677-686
43. Sass-Kortsak A.M., Corey P.N., and Robertson J.M. An investigation of the association between exposure to styrene and hearing loss. Ann. Epidemiol. 5 (1995) 15-24
44. Seidman M.D., Shivapuja B.G., and Quirk W.S. The protective effects of allopurinol and superoxide dismutase on noise-induced cochlear damage. Otolaryngol. Head Neck Surg. 109 (1993) 1052-1056
45. Sliwinska-Kowalska M., Zamyslowska-Szmytke E., Szymczak W., Kotylo P., Fiszer M., Wesolowski W., and Pawlaczyk-Luszczynska M. Ototoxic effects of occupational exposure to styrene and co-exposure to styrene and noise. J. Occup. Environ. Med. 45 (2003) 15-24
46. Vodicka P., Koskinen M., Vodickova L., Stetina R., Smerak P., Barta I., and Hemminki K. DNA adducts, strand breaks and micronuclei in mice exposed to styrene by inhalation. Chem. Biol. Interact. 137 (2001) 213-227
47. Yamane H., Nakai Y., Takayama M., Iguchi H., Nakagawa T., and Kojima A. Appearance of free radicals in the guinea pig inner ear after noise-induced acoustic trauma. Eur. Arch. Otorhinolaryngol. 252 (1995) 504-508
48. Yamane H., Nakai Y., Takayama M., Konishi K., Iguchi H., Nakagawa T., Shibata S., Kato A., Sunami K., and Kawakatsu C. The emergence of free radicals after acoustic trauma and strial blood flow. Acta. Otolaryngol. Suppl. (Stockh). 519 (1995) 87-92
49. Yang, W.P., Hu, B.H., Chen, G.D., Bielefeld, E.C., Henderson, D., 2008. Protective effect of N-acety-l-cysteine (l-NAC) against styrene-induced cochlear injuries. Acta Otolaryngol. 1-8 (First article).