Protective effects of vitamins E, B and C and L-carnitine in the prevention of cisplatin-induced ototoxicity in rats

被引:19
|
作者
Tokgoz, S. Alicura [1 ]
Vuralkan, E. [1 ]
Sonbay, N. D. [1 ]
Caliskan, M. [2 ]
Saka, C. [1 ]
Besalti, O. [2 ]
Akin, I. . [1 ]
机构
[1] Diskapi Yildirim Beyazit Training & Res Hosp, Minist Hlth, ENT Clin 1, Ankara, Turkey
[2] Ankara Univ, Fac Vet Med, TR-06100 Ankara, Turkey
来源
JOURNAL OF LARYNGOLOGY AND OTOLOGY | 2012年 / 126卷 / 05期
关键词
Ototoxicity; Cisplatin; Ear; Inner; Antioxidants; Rat; INDUCED HEARING-LOSS; ALPHA-TOCOPHEROL; 4-METHYLTHIOBENZOIC ACID; GUINEA-PIGS; TOXICITY; EFFICACY; AGENTS; NEPHROTOXICITY; CHEMOTHERAPY; ANTIOXIDANTS;
D O I
10.1017/S0022215112000382
中图分类号
R76 [耳鼻咽喉科学];
学科分类号
100213 ;
摘要
Objective: This experimental study aimed to investigate the effects of vitamins E, B and C and L-carnitine in preventing cisplatin-induced ototoxicity. Methods: Twenty-five adult, male, Wistar albino rats were randomly allocated to receive intraperitoneal cisplatin either alone or preceded by vitamins B, E or C or L-carnitine. Auditory brainstem response (i.e. hearing thresholds and wave I-IV intervals) and distortion product otoacoustic emissions (i.e. signal-to-noise ratios) were recorded before and 72 hours after cisplatin administration. Results: The following statistically significant differences were seen: control group pre-vs post-treatment wave I-IV interval values (p < 0.05); control vs vitamin E and B groups' I-IV interval values (p < 0.05); control vs other groups' hearing thresholds; vitamin E vs vitamin B and C and L-carnitine groups' hearing thresholds (p < 0.05); and vitamin B vs vitamin C and L-carnitine groups' hearing thresholds (p < 0.05). Statistically significant decreases were seen when comparing the initial and final signal-to-noise ratios in the control, vitamin B and L-carnitine groups (2000 and 3000 Hz; p < 0.01), and the initial and final signal-to-noise ratios in the control group (at 4000 Hz; p < 0.01). Conclusion: Vitamins B, E and C and L-carnitine appear to reduce cisplatin-induced ototoxicity in rats. The use of such additional treatments to decrease cisplatin-induced ototoxicity in humans is still under discussion.
引用
收藏
页码:464 / 469
页数:6
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