Vestibular toxicity of cis-2-pentenenitrile in the rat

dc.contributor.author
Saldaña-Ruíz, Sandra
dc.contributor.author
Hernández-Mir, Gerard
dc.contributor.author
Sedó Cabezón, Lara
dc.contributor.author
Cutillas Arroyo, Blanca
dc.contributor.author
Llorens i Baucells, Jordi
dc.date.issued
2013-12-04T10:55:42Z
dc.date.issued
2013-12-04T10:55:42Z
dc.date.issued
2012-06-20
dc.date.issued
2013-12-04T10:55:42Z
dc.identifier
0378-4274
dc.identifier
https://hdl.handle.net/2445/48279
dc.identifier
614216
dc.identifier
22546275
dc.description.abstract
cis-2-Pentenenitrile, an intermediate in the synthesis of nylon and other products, causes permanent behavioral deficits in rodents. Other low molecular weight nitriles cause degeneration either of the vestibular sensory hair cells or of selected neuronal populations in the brain. Adult male Long-Evans rats were exposed to cis-2-pentenenitrile (0, 1.25, 1.50, 1.75, or 2.0 mmol/kg, oral, in corn oil) and assessed for changes in open field activity and rating scores in a test battery for vestibular dysfunction. Surface preparations of the vestibular sensory epithelia were observed for hair cell loss using scanning electron microscopy. A separate experiment examined the impact of pre-treatment with the universal CYP inhibitor,1-aminobenzotriazole, on the effect of cis-2-pentenenitrile on vestibular rating scores. The occurrence of degenerating neurons in the central nervous system was assessed by Fluoro-Jade C staining. cis-2-Pentenenitrile had a dose-dependent effect on body weight. Rats receiving 1.50 mmol/kg or more of cis-2-pentenenitrile displayed reduced rearing activity in the open field and increased rating scores on the vestibular dysfunction test battery. Hair cell loss was observed in the vestibular sensory epithelia and correlated well with the behavioral deficits. Pre-treatment with 1-aminobenzotriazole blocked the behavioral effect. Fluoro-Jade C staining did not reveal significant neuronal degeneration in the central nervous system apart from neurite labeling in the olfactory glomeruli. We conclude that cis-2-pentenenitrile causes vestibular toxicity in a similar way to allylnitrile, cis-crotononitrile and 3,3′-iminodipropionitrile (IDPN), and also shares other targets such as the olfactory system with these other nitriles. The present data also suggest that CYP-mediated bioactivation is involved in cis-2-pentenenitrile toxicity.
dc.format
8 p.
dc.format
application/pdf
dc.language
eng
dc.publisher
Elsevier B.V.
dc.relation
Versió postprint del document publicat a: http://dx.doi.org/10.1016/j.toxlet.2012.04.010
dc.relation
Toxicology Letters, 2012, vol. 211, num. 3, p. 281-288
dc.relation
http://dx.doi.org/10.1016/j.toxlet.2012.04.010
dc.rights
(c) Elsevier Ireland Ltd, 2012
dc.rights
info:eu-repo/semantics/openAccess
dc.source
Articles publicats en revistes (Ciències Fisiològiques)
dc.subject
Equilibri (Fisiologia)
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Vertigen
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Malalties de l'orella
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Toxicologia
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Rates
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Nitrils
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Degeneració (Patologia)
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Equilibrium (Physiology)
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Vertigo
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Ear diseases
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Toxicology
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Rats
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Nitriles
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Degeneration (Pathology)
dc.title
Vestibular toxicity of cis-2-pentenenitrile in the rat
dc.type
info:eu-repo/semantics/article
dc.type
info:eu-repo/semantics/acceptedVersion


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