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晚用依他尼酸给药可降低外淋巴中庆大霉素的浓度并保护耳蜗毛细胞。

Late dosing with ethacrynic acid can reduce gentamicin concentration in perilymph and protect cochlear hair cells.

作者信息

Ding Dalian, McFadden Sandra L, Browne Richard W, Salvi Richard J

机构信息

Center for Hearing and Deafness, 215 Parker Hall, University at Buffalo, Buffalo, NY 14214, USA.

出版信息

Hear Res. 2003 Nov;185(1-2):90-6. doi: 10.1016/s0378-5955(03)00258-2.

Abstract

A key factor in the well-known interaction between ethacrynic acid (EA) and aminoglycoside antibiotics (AABs) is disruption of the blood-labyrinth barrier (BLB), leading to rapid entry of EA and AABs into the cochlear fluids. The idea that the blood-labyrinthine fluid concentration gradient might be utilized in a protective manner was tested in the current experiment. We hypothesized that administering EA when gentamicin (GM) levels are higher in the cochlea than in the blood might actually reduce cochlear damage by permitting efflux of GM from the cochlear fluids into the bloodstream, down a concentration gradient and across a temporarily disrupted BLB. Guinea pigs received 1, 11, 14 or 20 injections of GM (125 mg/kg i.m.). Approximately half of the animals also received a single injection of EA (40 mg/kg i.v.) either concurrently or 12-18 h after the last GM injection. Concurrent injection of EA significantly increased GM concentration in serum and perilymph at all time points sampled (2.5, 5-8, and 12 h post injection). Compared to animals that received GM only, animals that received a delayed injection of EA had a significantly lower GM concentration in perilymph, lower thresholds of the compound action potential, and less outer hair cell loss. Collectively, the evidence suggests that EA can reduce GM ototoxicity if it is administered 12-18 h after GM, but the mechanism remains to be elucidated. The results may have implications for the clinical management of aminoglycoside ototoxicity in humans, as well as for understanding the mechanisms underlying AAB/EA interactions.

摘要

依他尼酸(EA)与氨基糖苷类抗生素(AABs)之间著名的相互作用中的一个关键因素是血迷路屏障(BLB)的破坏,导致EA和AABs迅速进入耳蜗内淋巴液。在当前实验中,对利用血迷路内淋巴液浓度梯度进行保护的想法进行了测试。我们假设,当耳蜗中庆大霉素(GM)水平高于血液中GM水平时给予EA,实际上可能会通过使GM从耳蜗内淋巴液顺着浓度梯度并穿过暂时破坏的BLB流入血液,从而减少耳蜗损伤。豚鼠接受1、11、14或20次GM注射(125mg/kg,肌肉注射)。大约一半的动物在最后一次GM注射的同时或之后12 - 18小时还接受了一次EA注射(40mg/kg,静脉注射)。同时注射EA在所有采样时间点(注射后2.5、5 - 8和12小时)均显著提高了血清和外淋巴中GM的浓度。与仅接受GM的动物相比,接受延迟注射EA的动物外淋巴中GM浓度显著降低,复合动作电位阈值更低,外毛细胞损失更少。总体而言,证据表明,如果在GM注射后12 - 18小时给予EA,EA可以降低GM的耳毒性,但其机制仍有待阐明。这些结果可能对人类氨基糖苷类耳毒性的临床管理以及理解AAB/EA相互作用的潜在机制具有重要意义。

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