Are Intratympanic Injections of N-Acetylcysteine and Methylprednisolone Protective Against Cisplatin-Induced Ototoxicity?

被引:23
作者
Saliba, Issam [1 ]
El Fata, Fouad [4 ]
Ouelette, Valerie [2 ]
Robitaille, Yves [3 ]
机构
[1] Univ St Justine, Dept Otorhinolaryngol Head & Neck Surg, Ctr Hosp, Montreal, PQ, Canada
[2] Univ St Justine, Dept Audiol, Ctr Hosp, Montreal, PQ, Canada
[3] Univ St Justine, Dept Pathol, Ctr Hosp, Montreal, PQ, Canada
[4] Univ Montreal, Div Otorhinolaryngol Head & Neck Surg, Montreal, PQ, Canada
来源
JOURNAL OF OTOLARYNGOLOGY-HEAD & NECK SURGERY | 2010年 / 39卷 / 03期
关键词
N-Acetylcysteine; cisplatin; hair cells; hearing loss; methylprednisolone; ototoxicity; GUINEA-PIG; CIS-DIAMMINEDICHLOROPLATINUM; SODIUM THIOSULFATE; IN-VIVO; AGENTS; PLATINUM; PREVENTION; RESPONSES; COCHLEA;
D O I
10.2310/7070.2010.090156
中图分类号
R76 [耳鼻咽喉科学];
学科分类号
100213 ;
摘要
Objective: To identify and to compare the protective effect of intratympanic injections of N-acetylcysteine (NAC) or methylprednisolone to prevent cisplatin-induced ototoxicity, to investigate inner ear protection using an electron microscope and to evaluate the effect of 4% NAC on the middle ear. Design: Experimental study. Setting: Basic ear research center at Sainte-Justine hospital. Methods: Ten Hartley guinea pigs were divided into two groups, according to the product used intratympanically (4% NAC or 62.5 mg/mL methylprednisolone) in one ear. The other ear was left as control. Cisplatin was administered intraperitoneally (3 mg/kg), once a week for 5 weeks. Main outcome measures: Auditory evoked brainstem responses were used to test hearing. The inner ear was screened using an electron microscope. Results: Significant threshold shift was seen on all tested frequencies of both groups. This difference is clinically and statistically significant in the methylprednisolone group. The NAC-treated group had a lower threshold shift than the methylprednisolone group in both ears. Electron microscope studies showed in all untreated-NAC ears severe lesion of the inner and outer hair cells with complete degeneration of steriocilia, whereas in NAC-treated ears we noted a nuclear and cytoplasmic membrane preservation with some preservation of steriocila. Also, 4% intratympanic NAC produces an external auditory canal and middle ear inflammatory reaction. Conclusions: Intratympanic injections of methylprednisolone failed to demonstrate efficacy in protecting cisplatin ototoxicity whereas 4% NAC showed a partial protection. The safety of intratympanic injections should be investigated in further studies, as possible systemic shift of the locally administered treatment is suspected.
引用
收藏
页码:236 / 243
页数:8
相关论文
共 24 条
[1]   CHARACTERISTICS AND DRUG RESPONSES OF COCHLEAR AND VESTIBULAR ADENYLATE-CYCLASE [J].
BAGGERSJOBACK, D ;
FILIPEK, CS ;
SCHACHT, J .
ARCHIVES OF OTO-RHINO-LARYNGOLOGY-ARCHIV FUR OHREN-NASEN-UND KEHLKOPFHEILKUNDE, 1980, 228 (03) :217-222
[2]   Strategies for prevention of toxicity caused by platinum-based chemotherapy: Review and summary of the Annual Meeting of the Blood-Brain Barrier Disruption Program, Gleneden Beach, Oregon, March 10, 2001 [J].
Blakley, BW ;
Cohen, JI ;
Doolittle, ND ;
Muldoon, LL ;
Campbell, KC ;
Dickey, DT ;
Neuwelt, EA .
LARYNGOSCOPE, 2002, 112 (11) :1997-2001
[3]  
Campbell Kathleen C M, 2003, J Am Acad Audiol, V14, P144
[4]   Dose-dependent effect of 8-day cisplatin administration upon the morphology of the albino guinea pig cochlea [J].
Cardinaal, RM ;
de Groot, JCMJ ;
Huizing, EH ;
Veldman, JE ;
Smoorenburg, GF .
HEARING RESEARCH, 2000, 144 (1-2) :135-146
[5]   Prevention of cisplatin ototoxicity using transtympanic N-acetylcysteine and lactate [J].
Choe, WT ;
Chinosornvatana, N ;
Chang, KW .
OTOLOGY & NEUROTOLOGY, 2004, 25 (06) :910-915
[6]   THE COMPARATIVE EFFECTS OF SODIUM THIOSULFATE, DIETHYLDITHIOCARBAMATE, FOSFOMYCIN AND WR-2721 ON AMELIORATING CISPLATIN-INDUCED OTOTOXICITY [J].
CHURCH, MW ;
KALTENBACH, JA ;
BLAKLEY, BW ;
BURGIO, DL .
HEARING RESEARCH, 1995, 86 (1-2) :195-203
[7]   Protection against cisplatin-induced toxicities by N-acetylcysteine and sodium thiosulfate as assessed at the molecular, cellular, and in vivo levels [J].
Dickey, DT ;
Wu, YJ ;
Muldoon, LL ;
Neuwelt, EA .
JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2005, 314 (03) :1052-1058
[8]   CIS-DIAMMINEDICHLOROPLATINUM (II) OTOTOXICITY IN THE GUINEA-PIG [J].
ESTREM, SA ;
BABIN, RW ;
MOORE, KC .
OTOLARYNGOLOGY-HEAD AND NECK SURGERY, 1981, 89 (04) :638-645
[9]  
JUHN SK, 1988, ACTA OTO-LARYNGOL, P43
[10]   Comparison of five agents in protecting the cochlea against the ototoxic effects of cisplatin in the hamster [J].
Kaltenbach, JA ;
Church, MW ;
Blakley, BW ;
McCaslin, DL ;
Burgio, DL .
OTOLARYNGOLOGY-HEAD AND NECK SURGERY, 1997, 117 (05) :493-500