• 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

血管纹改变与顺铂耳毒性及恢复的关系。

Alterations in the stria vascularis in relation to cisplatin ototoxicity and recovery.

作者信息

Sluyter Steven, Klis Sjaak F L, de Groot John C M J, Smoorenburg Guido F

机构信息

Hearing Research Laboratories, Department of Otorhinolaryngology, University Medical Center Utrecht, Room G.02.531, P.O. Box 85.500, 3508 GA Utrecht, The Netherlands.

出版信息

Hear Res. 2003 Nov;185(1-2):49-56. doi: 10.1016/s0378-5955(03)00260-0.

DOI:10.1016/s0378-5955(03)00260-0
PMID:14599692
Abstract

We have investigated whether or not cisplatin-induced depression of the endocochlear potential (EP), and its subsequent recovery, possesses a morphological correlate in the stria vascularis. Guinea pigs implanted with round window electrodes were treated daily with cisplatin (1.5 mg/kg/day) until the compound action potential showed a profound hearing loss (> or =40 dB at 8 kHz after 5-18 days). Animals were either sacrificed immediately after the shift in hearing threshold ('SHORT' group) or allowed to recover for > or =4 weeks and subsequently sacrificed ('LONG' group). Control animals ('CONTROL' group) were not treated with cisplatin. Using stereological methods we measured the total strial cross-sectional area together with the areas occupied by the different strial components: the marginal, intermediate and basal cells. The total strial cross-sectional area in the basal turn of the LONG group was found to be significantly smaller than that of the SHORT and the CONTROL groups, whereas the EP was normal in the LONG group (in comparison to the CONTROL group) and markedly decreased in the SHORT group. The smaller area in the LONG group was mainly due to a decrease in the area occupied by the intermediate cells and to a lesser extent to a decrease in the marginal cell area. The area occupied by the basal cells did not change. Thus, the marked decrease in EP after 5-18 days of cisplatin administration was not related to shrinkage of the stria vascularis. Moreover, 4 weeks later the EP showed full recovery, whereas the stria vascularis had shrunk markedly.

摘要

我们研究了顺铂引起的内淋巴电位(EP)降低及其随后的恢复,是否与血管纹的形态学变化相关。给植入圆窗电极的豚鼠每日注射顺铂(1.5mg/kg/天),直至复合动作电位显示出严重听力损失(5-18天后在8kHz处≥40dB)。动物在听力阈值改变后立即处死(“SHORT”组),或让其恢复≥4周后处死(“LONG”组)。对照动物(“CONTROL”组)未用顺铂治疗。我们采用体视学方法测量了血管纹的总横截面积以及不同血管纹成分(边缘细胞、中间细胞和基底细胞)所占的面积。发现LONG组蜗底的血管纹总横截面积明显小于SHORT组和CONTROL组,而LONG组的EP正常(与CONTROL组相比),SHORT组则明显降低。LONG组面积减小主要是由于中间细胞所占面积减少,边缘细胞面积减少程度较小。基底细胞所占面积没有变化。因此,给予顺铂5-18天后EP的显著降低与血管纹萎缩无关。此外,4周后EP显示完全恢复,而血管纹已明显萎缩。

相似文献

1
Alterations in the stria vascularis in relation to cisplatin ototoxicity and recovery.血管纹改变与顺铂耳毒性及恢复的关系。
Hear Res. 2003 Nov;185(1-2):49-56. doi: 10.1016/s0378-5955(03)00260-0.
2
Cisplatin ototoxicity involves organ of Corti, stria vascularis and spiral ganglion: modulation by alphaMSH and ORG 2766.顺铂耳毒性涉及柯蒂氏器、血管纹和螺旋神经节:α-促黑素和ORG 2766的调节作用
Audiol Neurootol. 2003 Nov-Dec;8(6):305-15. doi: 10.1159/000073515.
3
Reversible cisplatin ototoxicity in the albino guinea pig.白化豚鼠中顺铂所致的可逆性耳毒性
Neuroreport. 2000 Feb 28;11(3):623-6. doi: 10.1097/00001756-200002280-00037.
4
A semiquantitative analysis of the effects of cisplatin on the rat stria vascularis.
Hear Res. 1998 Oct;124(1-2):44-59. doi: 10.1016/s0378-5955(98)00116-6.
5
Dose-dependent effect of 8-day cisplatin administration upon the morphology of the albino guinea pig cochlea.连续8天给予顺铂对白化豚鼠耳蜗形态的剂量依赖性效应。
Hear Res. 2000 Jun;144(1-2):135-46. doi: 10.1016/s0378-5955(00)00059-9.
6
Effect of Cochlear Implantation on the Endocochlear Potential and Stria Vascularis.人工耳蜗植入对内耳电位和血管纹的影响。
Otol Neurotol. 2021 Mar 1;42(3):e286-e293. doi: 10.1097/MAO.0000000000002949.
7
D-Methionine protects against cisplatin damage to the stria vascularis.
Hear Res. 1999 Dec;138(1-2):13-28. doi: 10.1016/s0378-5955(99)00142-2.
8
Cisplatin-induced ototoxicity: morphological evidence of spontaneous outer hair cell recovery in albino guinea pigs?顺铂诱导的耳毒性:白化豚鼠自发性外毛细胞恢复的形态学证据?
Hear Res. 2000 Jun;144(1-2):147-56. doi: 10.1016/s0378-5955(00)00060-5.
9
Time sequence of degeneration pattern in the guinea pig cochlea during cisplatin administration. A quantitative histological study.顺铂给药期间豚鼠耳蜗退变模式的时间序列。一项定量组织学研究。
Hear Res. 2004 Nov;197(1-2):44-54. doi: 10.1016/j.heares.2004.07.014.
10
Morphological correlates of hearing loss after cochlear implantation and electro-acoustic stimulation in a hearing-impaired Guinea pig model.听力受损豚鼠模型中人工耳蜗植入和电声刺激后听力损失的形态学关联
Hear Res. 2015 Sep;327:163-74. doi: 10.1016/j.heares.2015.06.007. Epub 2015 Jun 16.

引用本文的文献

1
The Role and Mechanism of GSDME-Dependent Pyroptosis in Cochlear Marginal Cells Injury by Cisplatin.GSDME 依赖性细胞焦亡在顺铂致耳蜗边缘细胞损伤中的作用及机制
Biomedicines. 2025 Jul 9;13(7):1680. doi: 10.3390/biomedicines13071680.
2
GSDMD-mediated mitochondrial dysfunction in marginal cells: A potential driver of inflammation and stria vascularis damage in CIHL.GSDMD介导的边缘细胞线粒体功能障碍:噪声性听力损失中炎症和血管纹损伤的潜在驱动因素
Proc Natl Acad Sci U S A. 2025 Mar 18;122(11):e2415805122. doi: 10.1073/pnas.2415805122. Epub 2025 Mar 11.
3
Hearing loss during chemotherapy: prevalence, mechanisms, and protection.
化疗期间的听力损失:患病率、机制及保护
Am J Cancer Res. 2024 Sep 25;14(9):4597-4632. doi: 10.62347/OKGQ4382. eCollection 2024.
4
Identification of common stria vascularis cellular alteration in sensorineural hearing loss based on ScRNA-seq.基于单细胞 RNA 测序的感音神经性听力损失中常见血管纹细胞改变的鉴定。
BMC Genomics. 2024 Feb 27;25(1):213. doi: 10.1186/s12864-024-10122-7.
5
NADPH Oxidase 3: Beyond the Inner Ear.NADPH氧化酶3:内耳之外
Antioxidants (Basel). 2024 Feb 8;13(2):219. doi: 10.3390/antiox13020219.
6
Cochlear Marginal Cell Pyroptosis Is Induced by Cisplatin NLRP3 Inflammasome Activation.顺铂诱导耳蜗边缘细胞焦亡及其机制研究。
Front Immunol. 2022 Apr 20;13:823439. doi: 10.3389/fimmu.2022.823439. eCollection 2022.
7
Preferential Cochleotoxicity of Cisplatin.顺铂的耳蜗毒性偏向性
Front Neurosci. 2021 Jul 26;15:695268. doi: 10.3389/fnins.2021.695268. eCollection 2021.
8
Cisplatin-Induced Stria Vascularis Damage Is Associated with Inflammation and Fibrosis.顺铂诱导的血管纹损伤与炎症和纤维化有关。
Neural Plast. 2020 Sep 22;2020:8851525. doi: 10.1155/2020/8851525. eCollection 2020.
9
Intratympanic Diltiazem-Chitosan Hydrogel as an Otoprotectant Against Cisplatin-Induced Ototoxicity in a Mouse Model.鼓室内地尔硫䓬-壳聚糖水凝胶作为一种耳保护剂对顺铂诱导的小鼠模型耳毒性的作用。
Otol Neurotol. 2020 Jan;41(1):115-122. doi: 10.1097/MAO.0000000000002417.
10
Assessment of the Effectiveness of Quercetin on Cisplatin-Induced Ototoxicity in Rats.槲皮素对顺铂诱导的大鼠耳毒性的有效性评估。
J Int Adv Otol. 2019 Aug;15(2):229-236. doi: 10.5152/iao.2019.5902.