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Assessment of gentamicin-induced vestibulotoxicity by click and galvanic vestibular-evoked myogenic potentials: a guinea pig investigation.

Authors :
Cheng PW
Lue JH
Lin CT
Day AS
Young YH
Source :
Neurotoxicology [Neurotoxicology] 2010 Jan; Vol. 31 (1), pp. 121-5. Date of Electronic Publication: 2009 Nov 05.
Publication Year :
2010

Abstract

Objective: The aim of this investigation carried out with guinea pigs was to study the possible effects of a gentamicin treatment on the saccular macula and on its afferent vestibular ganglion neurons.<br />Methods: The gentamicin-induced impairment was analyzed using vestibular-evoked myogenic potentials (VEMPs) elicited by both click and galvanic vestibular stimulations (GVS). Fifty microl of saline or gentamicin solution (40 mg/ml) was dropped over the round window membrane of the right (control) and left (lesion) cochleae, respectively. Four weeks after surgery, the VEMPs elicited with clicks and GVS were evaluated for each animal. Then, the animals were sacrificed in order to perform morphological and anti-Nav1.8 immunocytochemical analyses.<br />Results: Click- and GVS-VEMPs were obtained in all of the controls, whereas no potentials were obtained from gentamicin-treated animals. Lesions of sensory cells were observed in the saccular macula. In the injured vestibular ganglion, the percentage of voltage-gated sodium channel Nav1.8-like immunoreactive (Nav1.8-LI) neurons was significantly lower (38.9+/-0.7) than that (53.6+/-3.2) calculated in controls.<br />Conclusions: Gentamicin-induced impairments of the saccular macula and afferents of guinea pigs can be evaluated by recording both click- and GVS-VEMPs. Both tests provide information on the sacculo-collic reflex pathway and could help a clinical diagnosis of gentamicin intoxication by conventional eardrops in the patient with a perforated eardrum.<br /> (2009 Elsevier Inc. All rights reserved.)

Details

Language :
English
ISSN :
1872-9711
Volume :
31
Issue :
1
Database :
MEDLINE
Journal :
Neurotoxicology
Publication Type :
Academic Journal
Accession number :
19896499
Full Text :
https://doi.org/10.1016/j.neuro.2009.10.009