D-Methionine provides excellent protection from cisplatin ototoxicity in the rat

被引:181
作者
Campbell, KCM
Rybak, LP
Meech, RP
Hughes, L
机构
[1] Division of Otolaryngology, Department of Surgery, SIU School of Medicine, Springfield, IL 62794-1618
关键词
cisplatin; ototoxicity; methionine; protection;
D O I
10.1016/S0378-5955(96)00152-9
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
Cisplatin (CDDP) is a widely used chemotherapeutic agent. Unfortunately, CDDP is highly ototoxic. We tested D-methionine (D-Met), a sulfur containing compound, as an otoprotectant in male Wistar rats. Complete data sets were obtained for five groups of five animals each, including a treated control group (16 mg/kg CDDP), an untreated control group (administered an equivalent volume of saline) and three groups that received either 75, 150, or 300 mg/kg D-Met 30 min prior to the 16 mg/kg CDDP dosing. Auditory brainstem response (ABR) thresholds were obtained in response to clicks, and 1 kHz, 4 kHz, 8 kHz, and 14 kHz toneburst stimuli, before and 3 days after drug administration. Scanning electron microscopy (SEM) was used to examine the outer hair cells of the apical, middle and basal turns of the cochlea. Animal weight was measured on the first and final day. D-Met provided excellent otoprotection even at the lowest level with complete otoprotection obtained for the 300 mg/kg dosing as measured by both ABR and SEM. D-Met also markedly reduced weight loss and mortality. All animals receiving D-Met (15/15) survived to the end of the study period as opposed to only 5/10 of the treated controls.
引用
收藏
页码:90 / 98
页数:9
相关论文
共 69 条
[1]   SOME PROCEDURES TO REDUCE CIS-PLATINUM TOXICITY REDUCE ANTITUMOUR ACTIVITY [J].
AAMDAL, S ;
FODSTAD, O ;
PIHL, A .
CANCER TREATMENT REVIEWS, 1987, 14 (3-4) :389-395
[2]   AUDITORY TOXICITY EFFECTS OF LONG-TERM CIS-DICHLORODIAMMINEPLATINUM-II THERAPY IN GENITOURINARY CANCER-PATIENTS [J].
AGUILARMARKULIS, NV ;
BECKLEY, S ;
PRIORE, R ;
METTLIN, C .
JOURNAL OF SURGICAL ONCOLOGY, 1981, 16 (02) :111-123
[3]   EXACERBATION OF CISPLATIN-INDUCED NEPHROTOXICITY BY METHIONINE [J].
ALDEN, WW ;
REPTA, AJ .
CHEMICO-BIOLOGICAL INTERACTIONS, 1984, 48 (01) :121-124
[4]   PROTECTION AGAINST CISPLATIN TOXICITY BY ADMINISTRATION OF GLUTATHIONE ESTER [J].
ANDERSON, ME ;
NAGANUMA, A ;
MEISTER, A .
FASEB JOURNAL, 1990, 4 (14) :3251-3255
[5]   CISPLATIN - EVALUATION OF ITS OTOTOXIC POTENTIAL [J].
ANNIKO, M ;
SOBIN, A .
AMERICAN JOURNAL OF OTOLARYNGOLOGY, 1986, 7 (04) :276-293
[6]   PHASE-I TRIAL OF ESCALATING DOSES OF CISPLATIN IN HYPERTONIC SALINE [J].
BAJORIN, D ;
BOSL, GJ ;
FEIN, R .
JOURNAL OF CLINICAL ONCOLOGY, 1987, 5 (10) :1589-1593
[7]   MODIFICATION OF CISPLATIN TOXICITY WITH DIETHYLDITHIOCARBAMATE [J].
BERRY, JM ;
JACOBS, C ;
SIKIC, B ;
HALSEY, J ;
BORCH, RF .
JOURNAL OF CLINICAL ONCOLOGY, 1990, 8 (09) :1585-1590
[8]  
BERRY JM, 1989, P ASCO, V266, P69
[9]  
BLUMENREICH MS, 1985, CANCER, V55, P1118, DOI 10.1002/1097-0142(19850301)55:5<1118::AID-CNCR2820550529>3.0.CO
[10]  
2-5