ATTENUATION OF GENTAMICIN OTOTOXICITY BY GLUTATHIONE IN THE GUINEA-PIG IN-VIVO

被引:126
作者
GARETZ, SL [1 ]
ALTSCHULER, RA [1 ]
SCHACHT, J [1 ]
机构
[1] UNIV MICHIGAN,KRESGE HEARING RES INST,DEPT OTOLARYNGOL,ANN ARBOR,MI 48109
关键词
AMINOGLYCOSIDES; OTOTOXICITY; PROTECTION; GLUTATHIONE; FREE RADICALS; SCAVENGERS;
D O I
10.1016/0378-5955(94)90255-0
中图分类号
R36 [病理学]; R76 [耳鼻咽喉科学];
学科分类号
100104 ; 100213 ;
摘要
The effect of glutathione co-therapy on the expression of gentamicin ototoxicity was tested in pigmented guinea pigs. The first group of animals was injected with gentamicin (100 mg/kg body weight/day) for two weeks followed by 10 weeks of rest. A second group received glutathione by gastric gavage immediately prior to each gentamicin injection. Two groups of controls were treated either with saline injections or glutathione gavage alone. Auditory brainstem responses, taken at 2-week intervals, revealed a progressive gentamicin-induced hearing loss reaching a 30 to 40 dB threshold shift at 2 kHz, approximately 60 dB at 8 kHz and 80 dB at 18 kHz. Glutathione co-therapy slowed the progression of hearing loss and significantly attenuated the final threshold shifts by 20 to 40 dB. Morphological evaluation confirmed hair cell loss after gentamicin treatment and protection by glutathione. Drug serum levels were assayed at 2 and 7 days of treatment. There were no differences between the gentamicin (mean = 183 mu g/ml; range, 90 to 300) and the gentamicin/glutathione group (mean = 164 mu g/ml; range, 80 to 320). Antimicrobial activity of gentamicin was tested against Staphylococcus aureus and Pseudomonas aeruginosa. A 30-fold molar excess of glutathione did not influence the efficacy of gentamicin. These studies suggest that glutathione protects against ototoxicity by interfering with the cytotoxic mechanism.
引用
收藏
页码:81 / 87
页数:7
相关论文
共 25 条
[1]   COMPARISON OF REDUCED GLUTATHIONE WITH 2-MERCAPTOETHANE SULFONATE TO PREVENT CYCLOPHOSPHAMIDE-INDUCED UROTOXICITY [J].
CAVALLETTI, E ;
TOFANETTI, O ;
ZUNINO, F .
CANCER LETTERS, 1986, 32 (01) :1-6
[2]   FORMATION OF A TOXIC METABOLITE FROM GENTAMICIN BY A HEPATIC CYTOSOLIC FRACTION [J].
CRANN, SA ;
HUANG, MY ;
MCLAREN, JD ;
SCHACHT, J .
BIOCHEMICAL PHARMACOLOGY, 1992, 43 (08) :1835-1839
[3]  
DARROUZET J, 1967, REV LARYNGOL, V3, P187
[4]  
FEDERSPIL P, 1979, ANTIBIOTIKASCHADEN O, P86
[5]  
FEE WE, 1980, LARYNGOSCOPE S, V24, P1
[6]  
GARETZ S, 1993, ASS RES OTOLARYNGOL, V16, P141
[7]  
GARETZ S, 1992, ASS RES OTOLARYNGOL, V15, P110
[8]  
GARETZ S, 1994, IN PRESS HDB AUDITOR, V6
[9]  
GARETZ SL, 1994, IN PRESS HEAR RES
[10]  
HAGEN TM, 1990, AM J PHYSIOL, V259, pG524