2001
DOI: 10.1016/s0892-0362(00)00114-8
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Cochlear pathology induced by styrene

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Cited by 34 publications
(15 citation statements)
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“…Styrene exposure: 800 mg/kg by gavage, 1/day, 5 days/week, for 3 weeks. Gagnaire and Langlais, 2005;Lataye et al, 2000Lataye et al, , 2001Lataye et al, , 2003Loquet et al, 1999Loquet et al, , 2000Makitie et al, 2003). Our previous study showed that styrene exposure targeted OHCs and the related DCs and caused apoptosis, programmed cell death, which is believed to minimize the harmful effect of the cell death on neighboring cells .…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…Styrene exposure: 800 mg/kg by gavage, 1/day, 5 days/week, for 3 weeks. Gagnaire and Langlais, 2005;Lataye et al, 2000Lataye et al, , 2001Lataye et al, , 2003Loquet et al, 1999Loquet et al, , 2000Makitie et al, 2003). Our previous study showed that styrene exposure targeted OHCs and the related DCs and caused apoptosis, programmed cell death, which is believed to minimize the harmful effect of the cell death on neighboring cells .…”
Section: Discussionmentioning
confidence: 99%
“…It targets OHCs as well as Deiters cells (DCs) starting from the third row Gagnaire and Langlais, 2005;Lataye et al, 2000Lataye et al, , 2001Lataye et al, , 2003Loquet et al, 1999Loquet et al, , 2000Makitie et al, 2003 Abbreviations: CAP, compound action potential; DC, Deiters cell; FITC, fluorescein isothiocyanate; NIHL, noise-induced hearing loss; I/O, input/output; IHC, inner hair cell; IP, inner pillar cell; OHC, outer hair cell; OP, outer pillar cell; PBS, phosphate buffer saline; PTS, permanent threshold shift; SDH, succinate dehydrogenase; TNBTZ, tetranitro blue tetrazolium relatively insensitive to styrene exposure. Previously, we have observed that, even in cochleae in which all OHCs were missing, the maximal CAP amplitude was still at the normal level, indicating that the remaining IHCs were still functioning after the loss of all OHCs.…”
Section: Introductionmentioning
confidence: 99%
“…The location-dependency of the disruption was explained with distribution gradients of styrene measured in our previous report and antioxidants in the cochlea. Another characteristic of the styrene-induced disruption is that the degeneration starts from the third row of OHCs Gagnaire and Langlais, 2005;Lataye et al, 2000Lataye et al, , 2001Lataye et al, , 2003Loquet et al, 1999Loquet et al, , 2000Makitie et al, 2003), instead of the first row as seen in the noise-exposed cochlea. Our recent study revealed that Deiters cells were the most vulnerable target of styrene .…”
Section: The Ototoxic Effect Of Styrene In the Rat Cochleamentioning
confidence: 99%
“…Since these early studies, the ability of chemicals to directly disrupt auditory function has been established for trichloroethylene (Crofton et al 1993;Fechter et al 1998), toluene (Campo et al 1999;Crofton et al 1994;Johnson 1993), ethyl benzene (Cappaert et al 2001), and styrene , among other agents. In addition, Lataye et al (2001Lataye et al ( , 2003 have nicely identified the route by which solvents enter the cochlea and the pattern of damage that they produce in the inner ear.…”
Section: Ototoxicitymentioning
confidence: 99%