• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

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.

DOI:10.1016/s0378-5955(03)00258-2
PMID:14599696
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。

相似文献

1
Late dosing with ethacrynic acid can reduce gentamicin concentration in perilymph and protect cochlear hair cells.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。
Hear Res. 2003 Nov;185(1-2):90-6. doi: 10.1016/s0378-5955(03)00258-2.
2
Chinchilla models of selective cochlear hair cell loss.选择性耳蜗毛细胞损失的栗鼠模型
Hear Res. 2002 Dec;174(1-2):230-8. doi: 10.1016/s0378-5955(02)00697-4.
3
Dynamic changes following combined treatment with gentamicin and ethacrynic acid with and without acoustic stimulation. Cellular uptake and functional correlates.庆大霉素和依他尼酸联合治疗后,有无声刺激情况下的动态变化。细胞摄取及其功能关联。
Acta Otolaryngol. 1989 Nov-Dec;108(5-6):404-13. doi: 10.3109/00016488909125546.
4
Cellular and subcellular localization of tritiated gentamicin in the guinea pig cochlea following combined treatment with ethacrynic acid.依他尼酸联合治疗后豚鼠耳蜗中氚标记庆大霉素的细胞和亚细胞定位
Hear Res. 1992 Jan;57(2):157-65. doi: 10.1016/0378-5955(92)90148-g.
5
Mechanisms of rapid sensory hair-cell death following co-administration of gentamicin and ethacrynic acid.庆大霉素和依他尼酸联合给药后快速感觉毛细胞死亡的机制。
Hear Res. 2010 Jan;259(1-2):16-23. doi: 10.1016/j.heares.2009.08.008. Epub 2009 Aug 26.
6
Topical gentamicin and ethacrynic acid: effects on cochlear function.
Laryngoscope. 1998 Jul;108(7):1087-9. doi: 10.1097/00005537-199807000-00024.
7
Leupeptin protects cochlear and vestibular hair cells from gentamicin ototoxicity.亮抑酶肽可保护耳蜗和前庭毛细胞免受庆大霉素耳毒性的影响。
Hear Res. 2002 Feb;164(1-2):115-26. doi: 10.1016/s0378-5955(01)00417-8.
8
Gentamicin concentration gradients in scala tympani perilymph following systemic applications.全身应用后鼓阶外淋巴中庆大霉素的浓度梯度。
Audiol Neurootol. 2013;18(6):383-91. doi: 10.1159/000355283. Epub 2013 Nov 1.
9
Ototoxic effects of the interaction between kanamycin and ethacrynic acid. Cochlear ultrastructure correlated with cochlear potentials and kanamycin levels.卡那霉素与依他尼酸相互作用的耳毒性效应。耳蜗超微结构与耳蜗电位及卡那霉素水平的相关性。
Acta Otolaryngol. 1979;88(5-6):369-81. doi: 10.3109/00016487909137181.
10
A protein derived from the fusion of TAT peptide and FNK, a Bcl-x(L) derivative, prevents cochlear hair cell death from aminoglycoside ototoxicity in vivo.一种由TAT肽与Bcl-x(L)衍生物FNK融合而成的蛋白质可在体内预防氨基糖苷类耳毒性导致的耳蜗毛细胞死亡。
J Neurosci Res. 2007 May 15;85(7):1403-12. doi: 10.1002/jnr.21260.

引用本文的文献

1
The Blood-Labyrinth Barrier: Non-Invasive Delivery Strategies for Inner Ear Drug Delivery.血迷路屏障:内耳药物递送的非侵入性策略
Pharmaceutics. 2025 Apr 7;17(4):482. doi: 10.3390/pharmaceutics17040482.
2
Tissue engineering strategies for spiral ganglion neuron protection and regeneration.用于螺旋神经节神经元保护和再生的组织工程策略
J Nanobiotechnology. 2024 Jul 31;22(1):458. doi: 10.1186/s12951-024-02742-8.
3
Can auditory brain stem response accurately reflect the cochlear function?听觉脑干反应能否准确反映耳蜗功能?
J Neurophysiol. 2020 Dec 1;124(6):1667-1675. doi: 10.1152/jn.00233.2020. Epub 2020 Oct 7.
4
Functional and morphological analysis of different aminoglycoside treatment regimens inducing hearing loss in mice.诱导小鼠听力损失的不同氨基糖苷类治疗方案的功能和形态学分析
Exp Ther Med. 2019 Aug;18(2):1123-1130. doi: 10.3892/etm.2019.7687. Epub 2019 Jun 18.
5
Rapamycin Protects Spiral Ganglion Neurons from Gentamicin-Induced Degeneration In Vitro.雷帕霉素体外保护螺旋神经节神经元免受庆大霉素诱导的变性。
J Assoc Res Otolaryngol. 2019 Oct;20(5):475-487. doi: 10.1007/s10162-019-00717-3. Epub 2019 Jun 24.
6
Ototoxic effects and mechanisms of loop diuretics.袢利尿剂的耳毒性作用及机制。
J Otol. 2016 Dec;11(4):145-156. doi: 10.1016/j.joto.2016.10.001. Epub 2016 Oct 27.
7
Mannitol and the blood-labyrinth barrier.甘露醇与血迷路屏障。
J Otolaryngol Head Neck Surg. 2017 Dec 11;46(1):66. doi: 10.1186/s40463-017-0245-8.
8
Kanamycin Damages Early Postnatal, but Not Adult Spiral Ganglion Neurons.卡那霉素损伤早期产后,但不损伤成年耳蜗螺旋神经节神经元。
Neurotox Res. 2017 Nov;32(4):603-613. doi: 10.1007/s12640-017-9773-2. Epub 2017 Jun 27.
9
A Sox10(rtTA/+) Mouse Line Allows for Inducible Gene Expression in the Auditory and Balance Organs of the Inner Ear.一种Sox10(rtTA/+)小鼠品系可在内耳的听觉和平衡器官中实现诱导性基因表达。
J Assoc Res Otolaryngol. 2015 Jun;16(3):331-45. doi: 10.1007/s10162-015-0517-9. Epub 2015 Apr 21.
10
OTOTOXIC EFFECTS OF CARBOPLATIN IN ORGANOTYPIC CULTURES IN CHINCHILLAS AND RATS.卡铂对栗鼠和大鼠器官型培养物的耳毒性作用。
J Otol. 2012 Dec;7(2):92-101. doi: 10.1016/S1672-2930(12)50023-1.