GLUTATHIONE PROTECTION AGAINST GENTAMICIN OTOTOXICITY DEPENDS ON NUTRITIONAL-STATUS

Citation
J. Lautermann et al., GLUTATHIONE PROTECTION AGAINST GENTAMICIN OTOTOXICITY DEPENDS ON NUTRITIONAL-STATUS, Hearing research, 86(1-2), 1995, pp. 15-24
Citations number
37
Categorie Soggetti
Neurosciences,Acoustics
Journal title
ISSN journal
03785955
Volume
86
Issue
1-2
Year of publication
1995
Pages
15 - 24
Database
ISI
SICI code
0378-5955(1995)86:1-2<15:GPAGOD>2.0.ZU;2-E
Abstract
This study demonstrates that gentamicin ototoxicity depends on dietary factors and correlates with tissue glutathione levels. After 15 days of gentamicin injections (100 mg/kg/day s.c.) guinea pigs on a regular protein diet (18.5% protein) had an average hearing loss of 9 dB at 3 kHz, 31 dB at 8 khz and 42 dB at 18 kHz. Guinea pigs on a 7% protein diet showed an increased hearing loss of 52 dB at 3 kHz, 63 dB at 8 kH z and 74 dB at 18 kHz. Supplementing the low protein diet with either essential or sulfur-containing amino acids did not protect against gen tamicin ototoxicity. Glutathione levels in the cochlear sensory epithe lium were decreased in animals on a low protein diet and could be rest ored to normal by oral administration of glutathione monoethyl ester ( 1.2 g/kg/day) in combination with vitamin C (100 mg/kg/day). Glutathio ne supplementation significantly reduced the magnitude of hearing loss in the low protein diet group at all frequencies (43 dB reduction at 3 kHz, 27 dB reduction at 8 kHz and 21 dB reduction at 18 kHz). In ani mals on a full protein diet, dietary glutathione neither increased coc hlear glutathione levels nor attenuated hearing loss. Serum gentamicin levels did not differ between animals on the various diets with or wi thout glutathione supplement. These results suggest that gentamicin to xicity and detoxifying mechanisms are affected by the metabolic state of the animal and the glutathione content of the tissue. Thus, compoun ds that could potentially protect against gentamicin ototoxicity may b e more correctly assessed in animal models of deficient nutritional st ates in which endogenous detoxifying mechanisms are compromised. This animal model might also be more realistically related to the clinical situation of a critically ill patient receiving gentamicin treatment.