Protection against cisplatin-induced ototoxicity by N-acetylcysteine in a rat model

被引:107
作者
Dickey, DT
Muldoon, LL
Kraemer, DF
Neuwelt, EA [1 ]
机构
[1] Oregon Hlth & Sci Univ, Dept Neurol, Portland, OR 97201 USA
[2] Oregon Hlth & Sci Univ, Dept Neurosurg, Portland, OR 97201 USA
[3] Oregon Hlth & Sci Univ, Dept Cell & Dev Biol, Portland, OR 97201 USA
[4] Oregon Hlth & Sci Univ, Dept Med Informat & Clin Epidemiol, Portland, OR 97201 USA
[5] Vet Adm Med Ctr, Portland, OR 97201 USA
关键词
cisplatin; N-acetylcysteine; ototoxicity; chemoprotection; blood-brain barrier; animal model;
D O I
10.1016/j.heares.2004.02.007
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 that is highly ototoxic. Animal studies and clinical trials have shown that thiosulfates can protect against platinum-induced ototoxicity. This study investigated a new model for CDDP ototoxicity in the rat, and tested the potential chemoprotective effect of administering N-acetylcysteine (NAC) before giving CDDP. Long Evans rats were treated with CDDP 6 mg/kg delivered to the aorta via a retrograde right external carotid artery infusion, 15 min after intravenous (IV) infusion of saline (n = 8) or NAC 400 mg/kg (n = 8), such that the vertebral arteries were perfused. Subsequent groups were similarly treated with NAC 30 min before (n = 7) and 4 h after (n = 7) CDDP. Auditory brainstem response (ABR) thresholds were tested at 4-20 kHz, 7 days after treatment and compared to baseline ABR values. The NAC-treated rats exhibited no significant change from baseline values at all time intervals, while the saline-treated rats showed marked ototoxicity, especially at higher frequencies. Furthermore, the rats treated with NAC 15 min before CDDP exhibited less overall toxicity to CDDP, as evidenced in weight loss 7 days post-treatment (mean for saline = -39.63 g; mean for NAC = -21.13 g; p = 0.0084). These data show that treatment with NAC can prevent CDDP-induced ototoxicity in rats. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:25 / 30
页数:6
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