Flavanoid of Drynaria fortunei protects against gentamicin ototoxicity

被引:20
作者
Long, M [1 ]
Smouha, EE
Qiu, D
Li, FR
Johnson, F
Luft, B
机构
[1] SUNY Stony Brook, Dept Med, Stony Brook, NY 11794 USA
[2] SUNY Stony Brook, Div Otolaryngol Head & Neck Surg, Stony Brook, NY 11794 USA
[3] SUNY Stony Brook, Dept Chem, Stony Brook, NY 11794 USA
关键词
Dynaria fortunei; Gu Sui Bu; flavanoid; hair cell repairing; gentamicin; ototoxicity;
D O I
10.1002/ptr.1505
中图分类号
R914 [药物化学];
学科分类号
100701 [药物化学];
摘要
A flavanoid fraction (FF) from Drynaria fortunei, was investigated to see if it has the protective and ameliorative effects against gentamicin (GM) ototoxicity in guinea pigs (n = 36). Eleven (GM-group) animals received GM 100 mg/kg/day. Eleven (GMFF-group) animals received the same dose of GM but 2 days prior were dosed with FF (10 mg/kg/day) for 2 weeks. Seven (S-group) animals received saline and seven (FF-group) animals received the same dose of FF as the GMFF-group. The thresholds of tone-burst auditory evoked response (ABR) at 2 k, 8 k, and 32 k Hz were determined to be as follows: GM-group: 90 dB, 92 dB and 72 dB, GMFF-group: 30 dB, 37 dB and 38 dB, FF-group: 28 dB, 25 dB and 29 dB, S-group: 30 dB, 28 dB and 39 dB. The GM-group had a significantly higher hearing threshold than the other groups (p < 0.05). The GMFF- and FF-groups had hearing thresholds similar to the S-groups (p > 0.1). Repair of damaged hair cells was observed histologically. The percentage of the damaged outer hair cells (OHC) and inner hair cells (IHC) were determined to be as follows: GM-group: 43% and 20%, GMFF-group: 20% and 2%, FF-group: 9% and 2% and S-group: 4% and 1%. The GMFF-group showed less damage to the OHC (p > 0.05) and significantly less damage to the IHC (p < 0.05) than the GM-group. FF did not change the antimicrobial activity of GM and it did not show any intrinsic antibacterial effect. FF did not affect the kinetics of GM during the course of the experiment. Copyright (C) 2004 John Wiley Sons, Ltd.
引用
收藏
页码:609 / 614
页数:6
相关论文
共 18 条
[1]
BENSON CA, 1994, CLIN INFECT DIS S3, V18, P237
[2]
Leupeptin protects cochlear and vestibular hair cells from gentamicin ototoxicity [J].
Ding, DL ;
Stracher, A ;
Salvi, RJ .
HEARING RESEARCH, 2002, 164 (1-2) :115-126
[3]
D-Methionine and cisplatin ototoxicity in the guinea pig:: D-methionine influences cisplatin pharmacokinetics [J].
Ekborn, A ;
Laurell, G ;
Johnström, P ;
Wallin, I ;
Eksborg, S ;
Ehrsson, H .
HEARING RESEARCH, 2002, 165 (1-2) :53-61
[4]
Feghali J G, 1998, Ear Nose Throat J, V77, P282
[5]
Feghali J.G., 1998, ENT-EAR NOSE THROAT, V77, P280
[6]
Feghali JG, 1998, ENT-EAR NOSE THROAT, V77, P282
[7]
Aminoglycoside antibiotics [J].
Forge, A ;
Schacht, J .
AUDIOLOGY AND NEURO-OTOLOGY, 2000, 5 (01) :3-22
[8]
A radical demise - Toxins and trauma share common pathways in hair cell death [J].
Kopke, R ;
Allen, KA ;
Henderson, D ;
Hoffer, M ;
Frenz, D ;
Van de Water, T .
OTOTOXICITY: BASIC SCIENCE AND CLINICAL APPLICATIONS, 1999, 884 :171-191
[9]
M40403, a superoxide dismutase mimetic, protects cochlear hair cells from gentamicin, but not cisplatin toxicity [J].
McFadden, SL ;
Ding, DL ;
Salvemini, D ;
Salvi, RJ .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 2003, 186 (01) :46-54
[10]