• 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

OCT2在不同物种耳蜗中的免疫组织化学定位。

Immunohistochemical localization of OCT2 in the cochlea of various species.

作者信息

Hellberg Victoria, Gahm Caroline, Liu Wei, Ehrsson Hans, Rask-Andersen Helge, Laurell Göran

机构信息

Department of Clinical Science, Intervention and Technology.

Department of Surgical Sciences, Uppsala University, Uppsala, Sweden.

出版信息

Laryngoscope. 2015 Sep;125(9):E320-5. doi: 10.1002/lary.25304. Epub 2015 Apr 17.

DOI:10.1002/lary.25304
PMID:25892279
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5132114/
Abstract

OBJECTIVE

To locate the organic cation transporter 2 (OCT2) in the cochlea of three different species and to modulate the ototoxicity of cisplatin in the guinea pig by pretreatment with phenformin, having a known affinity for OCT2.

STUDY DESIGN

Immunohistochemical and in vivo study.

METHODS

Sections from the auditory end organs were subjected to immunohistochemical staining in order to identify OCT2 in cochlea from untreated rats, guinea pigs, and a pig. In the in vivo study, guinea pigs were given phenformin intravenously 30 minutes before cisplatin administration. Electrophysiological hearing thresholds were determined, and hair cells loss was assessed 96 hours later. The total amount of platinum in cochlear tissue was determined using mass spectrometry.

RESULTS

Organic cation transporter 2 was found in the supporting cells and in type I spiral ganglion cells in the cochlea of all species studied. Pretreatment with phenformin did not reduce the ototoxic side effect of cisplatin. Furthermore, the concentration of platinum in the cochlea was not affected by phenformin.

CONCLUSIONS

The localization of OCT2 in the supporting cells and type I spiral ganglion cells suggests that this transport protein is not primarily involved in cisplatin uptake from the systemic circulation. We hypothesize that OCT2 transport intensifies cisplatin ototoxicity via transport mechanisms in alternate compartments of the cochlea.

LEVEL OF EVIDENCE

N/A.

摘要

目的

在三种不同物种的耳蜗中定位有机阳离子转运体2(OCT2),并通过用对OCT2具有已知亲和力的苯乙双胍预处理来调节顺铂在豚鼠中的耳毒性。

研究设计

免疫组织化学和体内研究。

方法

对听觉终器的切片进行免疫组织化学染色,以鉴定未处理的大鼠、豚鼠和猪的耳蜗中的OCT2。在体内研究中,在给予顺铂前30分钟静脉注射苯乙双胍给豚鼠。测定电生理听力阈值,并在96小时后评估毛细胞损失。使用质谱法测定耳蜗组织中的铂总量。

结果

在所研究的所有物种的耳蜗中,在支持细胞和I型螺旋神经节细胞中发现了有机阳离子转运体2。用苯乙双胍预处理并未降低顺铂的耳毒性副作用。此外,耳蜗中的铂浓度不受苯乙双胍的影响。

结论

OCT2在支持细胞和I型螺旋神经节细胞中的定位表明,这种转运蛋白并非主要参与从体循环中摄取顺铂。我们推测,OCT2转运通过耳蜗其他隔室中的转运机制增强了顺铂耳毒性。

证据水平

无。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aaeb/5132114/89ffa0434d34/LARY-125-E320-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aaeb/5132114/7b2e2808b1ee/LARY-125-E320-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aaeb/5132114/89ffa0434d34/LARY-125-E320-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aaeb/5132114/7b2e2808b1ee/LARY-125-E320-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aaeb/5132114/89ffa0434d34/LARY-125-E320-g002.jpg

相似文献

1
Immunohistochemical localization of OCT2 in the cochlea of various species.OCT2在不同物种耳蜗中的免疫组织化学定位。
Laryngoscope. 2015 Sep;125(9):E320-5. doi: 10.1002/lary.25304. Epub 2015 Apr 17.
2
MATE1 expression in the cochlea and its potential involvement in cisplatin cellular uptake and ototoxicity.MATE1在耳蜗中的表达及其在顺铂细胞摄取和耳毒性中的潜在作用。
Acta Otolaryngol. 2023 Mar;143(3):242-249. doi: 10.1080/00016489.2023.2184864. Epub 2023 Mar 21.
3
Organic cation transporter 2 mediates cisplatin-induced oto- and nephrotoxicity and is a target for protective interventions.有机阳离子转运体 2 介导顺铂诱导的耳肾毒性,是保护性干预的靶点。
Am J Pathol. 2010 Mar;176(3):1169-80. doi: 10.2353/ajpath.2010.090610. Epub 2010 Jan 28.
4
Immunohistochemical detection of platinated DNA in the cochlea of cisplatin-treated guinea pigs.顺铂处理的豚鼠耳蜗中铂化DNA的免疫组织化学检测。
Hear Res. 2005 May;203(1-2):112-21. doi: 10.1016/j.heares.2004.12.007.
5
Interaction of Cisplatin with the human organic cation transporter 2.顺铂与人有机阳离子转运体2的相互作用。
Clin Cancer Res. 2008 Jun 15;14(12):3875-80. doi: 10.1158/1078-0432.CCR-07-4793.
6
Saving ears and kidneys from cisplatin.从顺铂中拯救耳朵和肾脏。
Anticancer Res. 2013 Oct;33(10):4183-8.
7
Blood flow-independent accumulation of cisplatin in the guinea pig cochlea.顺铂在豚鼠耳蜗中的血流非依赖性蓄积。
Acta Otolaryngol. 1997 Jan;117(1):55-60. doi: 10.3109/00016489709117992.
8
Contribution of organic cation transporter 2 (OCT2) to cisplatin-induced nephrotoxicity.有机阳离子转运体2(OCT2)在顺铂诱导的肾毒性中的作用。
Clin Pharmacol Ther. 2009 Oct;86(4):396-402. doi: 10.1038/clpt.2009.139. Epub 2009 Jul 22.
9
Cisplatin and oxaliplatin toxicity: importance of cochlear kinetics as a determinant for ototoxicity.顺铂和奥沙利铂的毒性:耳蜗动力学作为耳毒性决定因素的重要性。
J Natl Cancer Inst. 2009 Jan 7;101(1):37-47. doi: 10.1093/jnci/djn418. Epub 2008 Dec 30.
10
[Effectiveness of cisplatin on the expressions of Bcl-2 and Bax in cochlea and spiral ganglion cells of guinea pigs].[顺铂对豚鼠耳蜗及螺旋神经节细胞中Bcl-2和Bax表达的影响]
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2016 Jan;30(1):45-8.

引用本文的文献

1
Supporting Cells and Their Potential Roles in Cisplatin-Induced Ototoxicity.支持细胞及其在顺铂诱导的耳毒性中的潜在作用
Front Neurosci. 2022 Apr 27;16:867034. doi: 10.3389/fnins.2022.867034. eCollection 2022.
2
The Mechanotransduction Channel and Organic Cation Transporter Are Critical for Cisplatin Ototoxicity in Murine Hair Cells.机械转导通道和有机阳离子转运体对小鼠毛细胞顺铂耳毒性至关重要。
Front Mol Neurosci. 2022 Feb 10;15:835448. doi: 10.3389/fnmol.2022.835448. eCollection 2022.
3
Organic Cation Transporters in Human Physiology, Pharmacology, and Toxicology.

本文引用的文献

1
Cisplatin and oxaliplatin are toxic to cochlear outer hair cells and both target thioredoxin reductase in organ of Corti cultures.顺铂和奥沙利铂对耳蜗外毛细胞有毒性,且两者在柯蒂氏器培养物中均靶向硫氧还蛋白还原酶。
Acta Otolaryngol. 2014 May;134(5):448-54. doi: 10.3109/00016489.2013.879740.
2
Conjunctive therapy of cisplatin with the OCT2 inhibitor cimetidine: influence on antitumor efficacy and systemic clearance.顺铂联合 OCT2 抑制剂西咪替丁治疗:对抗肿瘤疗效和全身清除率的影响。
Clin Pharmacol Ther. 2013 Nov;94(5):585-92. doi: 10.1038/clpt.2013.145. Epub 2013 Jul 17.
3
Perivascular macrophage-like melanocyte responsiveness to acoustic trauma--a salient feature of strial barrier associated hearing loss.
人体生理学、药理学和毒理学中的有机阳离子转运体。
Int J Mol Sci. 2020 Oct 24;21(21):7890. doi: 10.3390/ijms21217890.
4
Current Strategies to Combat Cisplatin-Induced Ototoxicity.对抗顺铂诱导耳毒性的当前策略
Front Pharmacol. 2020 Jul 3;11:999. doi: 10.3389/fphar.2020.00999. eCollection 2020.
5
The Role of the Reactive Oxygen Species Scavenger Agent, Astaxanthin, in the Protection of Cisplatin-Treated Patients Against Hearing Loss.活性氧清除剂虾青素在保护顺铂治疗患者免受听力损失方面的作用。
Drug Des Devel Ther. 2019 Dec 18;13:4291-4303. doi: 10.2147/DDDT.S212313. eCollection 2019.
6
Hydrogen Inhalation Protects against Ototoxicity Induced by Intravenous Cisplatin in the Guinea Pig.氢气吸入可保护豚鼠免受静脉注射顺铂所致的耳毒性。
Front Cell Neurosci. 2017 Sep 13;11:280. doi: 10.3389/fncel.2017.00280. eCollection 2017.
7
An integrated view of cisplatin-induced nephrotoxicity and ototoxicity.顺铂诱导的肾毒性和耳毒性的综合观点。
Toxicol Lett. 2015 Sep 17;237(3):219-27. doi: 10.1016/j.toxlet.2015.06.012. Epub 2015 Jun 20.
血管周巨噬细胞样黑素细胞对声创伤的反应性——与嵴相关的听力损失的一个显著特征。
FASEB J. 2013 Sep;27(9):3730-40. doi: 10.1096/fj.13-232892. Epub 2013 May 31.
4
Transport of biguanides by human organic cation transporter OCT2.人有机阳离子转运体 OCT2 对双胍类药物的转运。
Biomed Pharmacother. 2013 Jun;67(5):425-30. doi: 10.1016/j.biopha.2013.02.003. Epub 2013 Feb 27.
5
Organic cation transporter OCTs (SLC22) and MATEs (SLC47) in the human kidney.人肾脏中的有机阳离子转运体 OCTs(SLC22)和 MATEs(SLC47)。
AAPS J. 2013 Apr;15(2):581-8. doi: 10.1208/s12248-013-9465-7. Epub 2013 Feb 22.
6
Endothelial cell, pericyte, and perivascular resident macrophage-type melanocyte interactions regulate cochlear intrastrial fluid-blood barrier permeability.内皮细胞、周细胞和血管周驻留巨噬细胞样黑素细胞相互作用调节耳蜗内间质液-血液屏障通透性。
J Assoc Res Otolaryngol. 2013 Apr;14(2):175-85. doi: 10.1007/s10162-012-0365-9. Epub 2012 Dec 18.
7
Role of organic cation/carnitine transporter 1 in uptake of phenformin and inhibitory effect on complex I respiration in mitochondria.有机阳离子/肉碱转运体 1 在摄取苯乙双胍和抑制线粒体复合体 I 呼吸中的作用。
Toxicol Sci. 2013 Mar;132(1):32-42. doi: 10.1093/toxsci/kfs330. Epub 2012 Dec 5.
8
Perivascular-resident macrophage-like melanocytes in the inner ear are essential for the integrity of the intrastrial fluid-blood barrier.内耳血管周围驻留的巨噬细胞样黑素细胞对于内淋巴液-血液屏障的完整性至关重要。
Proc Natl Acad Sci U S A. 2012 Jun 26;109(26):10388-93. doi: 10.1073/pnas.1205210109. Epub 2012 Jun 11.
9
Prevention of cisplatin-induced hearing loss by administration of a thiosulfate-containing gel to the middle ear in a guinea pig model.通过向豚鼠模型的中耳施用含硫代硫酸盐的凝胶来预防顺铂诱导的听力损失。
Cancer Chemother Pharmacol. 2011 Dec;68(6):1547-56. doi: 10.1007/s00280-011-1656-2. Epub 2011 May 2.
10
Co-administration of cisplatin and furosemide causes rapid and massive loss of cochlear hair cells in mice.顺铂和呋塞米联合给药导致小鼠耳蜗毛细胞迅速大量丧失。
Neurotox Res. 2011 Nov;20(4):307-19. doi: 10.1007/s12640-011-9244-0. Epub 2011 Apr 1.