• 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

豚鼠耳蜗中,Akt和c-Jun氨基末端激酶在中度噪声暴露后受到调节。

Akt and c-Jun N-terminal kinase are regulated in response to moderate noise exposure in the cochlea of guinea pigs.

作者信息

Selivanova Oxana, Brieger Jürgen, Heinrich Ulf-Rüdiger, Mann Wolf

机构信息

Department of Otorhinolaryngology, Mainz Medical School, Mainz, Germany.

出版信息

ORL J Otorhinolaryngol Relat Spec. 2007;69(5):277-82. doi: 10.1159/000103871. Epub 2007 Jun 12.

DOI:10.1159/000103871
PMID:17565230
Abstract

The molecular mechanisms induced in the inner ear after noise exposure are not well understood. Akt and c-Jun N-terminal kinase (JNK) are key factors of signaling pathways balancing cellular survival and apoptosis. Therefore, we analyzed the spatial distribution of Akt, JNK, their respective activated (i.e. phosphorylated) forms, p-Akt and p-JNK, as well as NF kappa B by immunohistochemistry after 70- and 90-dB noise exposure in an animal model. Alterations of the expression patterns compared to unexposed animals were quantified by a computer-based image analysis method. In unexposed specimens, Akt, p-Akt, JNK, p-JNK were found to be commonly expressed in different regions of the cochlea, whereas NF kappa B was exclusively restricted to the lateral wall. After noise stimulation, the expression of the different molecules was downregulated with the exception of JNK. JNK remained largely unchanged or increased JNK levels were identified in ganglion cells and Schwann cells after 70 dB as well as in the unstained nerve fibers. The stable or increasing levels of JNK might be indicative of a preapoptotic state. The downregulation of Akt in the cochlea might support these activities. p-Akt was not reduced in the spiral ganglion cells after 90-dB exposure and was upregulated in the unstained nerve fibers, probably indicating a counteracting prosurvival cellular reaction in these tissues. In conclusion, we suggest that the observed alterations in both the Akt and JNK pathways are part of a noise distress-induced response indicating pro- and antiapoptotic activities in the different tissues of the cochlea.

摘要

噪声暴露后内耳诱导的分子机制尚未完全明确。Akt和c-Jun氨基末端激酶(JNK)是平衡细胞存活和凋亡的信号通路的关键因子。因此,我们通过免疫组织化学分析了动物模型在70分贝和90分贝噪声暴露后Akt、JNK、它们各自的活化(即磷酸化)形式p-Akt和p-JNK以及核因子κB的空间分布。通过基于计算机的图像分析方法对与未暴露动物相比的表达模式变化进行了量化。在未暴露的标本中,发现Akt、p-Akt、JNK、p-JNK在耳蜗的不同区域普遍表达,而核因子κB仅局限于侧壁。噪声刺激后,除JNK外,不同分子的表达均下调。70分贝噪声暴露后,JNK在很大程度上保持不变,或在神经节细胞和施万细胞以及未染色的神经纤维中JNK水平升高。JNK水平稳定或升高可能表明处于凋亡前期状态。耳蜗中Akt的下调可能支持这些活动。90分贝暴露后,螺旋神经节细胞中的p-Akt没有降低,且在未染色的神经纤维中上调,这可能表明这些组织中存在对抗细胞存活的反应。总之,我们认为观察到的Akt和JNK通路的改变是噪声应激诱导反应的一部分,表明耳蜗不同组织中存在促凋亡和抗凋亡活动。

相似文献

1
Akt and c-Jun N-terminal kinase are regulated in response to moderate noise exposure in the cochlea of guinea pigs.豚鼠耳蜗中,Akt和c-Jun氨基末端激酶在中度噪声暴露后受到调节。
ORL J Otorhinolaryngol Relat Spec. 2007;69(5):277-82. doi: 10.1159/000103871. Epub 2007 Jun 12.
2
Anti-apoptotic role of retinoic acid in the inner ear of noise-exposed mice.视黄酸在噪声暴露小鼠内耳中的抗凋亡作用。
Biochem Biophys Res Commun. 2005 Sep 23;335(2):485-90. doi: 10.1016/j.bbrc.2005.07.114.
3
COX-2 expression in the guinea pig cochlea is partly altered by moderate sound exposure.
Neurosci Lett. 2006 Feb 13;394(2):121-6. doi: 10.1016/j.neulet.2005.10.039. Epub 2005 Nov 10.
4
Fast alterations of vascular endothelial growth factor (VEGF) expression and that of its receptors (Flt-1, Flk-1 and Neuropilin) in the cochlea of guinea pigs after moderate noise exposure.中度噪声暴露后豚鼠耳蜗中血管内皮生长因子(VEGF)及其受体(Flt-1、Flk-1和神经纤毛蛋白)表达的快速变化。
Eur Arch Otorhinolaryngol. 2007 Feb;264(2):121-8. doi: 10.1007/s00405-006-0154-3. Epub 2006 Oct 10.
5
Stress and survival pathways in the mammalian cochlea.哺乳动物耳蜗中的应激与生存途径。
Audiol Neurootol. 2010;15(5):282-90. doi: 10.1159/000279760. Epub 2010 Feb 3.
6
[Study of the effect of JNK signal transduction pathway in intense noise-induced apoptosis in cochlea of guinea pig].
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2009 Dec;23(24):1138-42.
7
Noise exposure alters cyclooxygenase 1 (COX-1) and 5-lipoxygenase (5-LO) expression in the guinea pig cochlea.噪声暴露会改变豚鼠耳蜗中环氧合酶1(COX-1)和5-脂氧合酶(5-LO)的表达。
Acta Otolaryngol. 2010 Mar;130(3):358-65. doi: 10.1080/00016480903168066.
8
Wnt-11 signaling leads to down-regulation of the Wnt/beta-catenin, JNK/AP-1 and NF-kappaB pathways and promotes viability in the CHO-K1 cells.Wnt-11信号传导导致Wnt/β-连环蛋白、JNK/AP-1和NF-κB信号通路的下调,并促进CHO-K1细胞的活力。
Exp Cell Res. 2008 Aug 1;314(13):2389-99. doi: 10.1016/j.yexcr.2008.04.010. Epub 2008 May 3.
9
EV71 induces VCAM-1 expression via PDGF receptor, PI3-K/Akt, p38 MAPK, JNK and NF-kappaB in vascular smooth muscle cells.肠道病毒71型通过血小板衍生生长因子受体、磷脂酰肌醇-3激酶/蛋白激酶B、p38丝裂原活化蛋白激酶、应激活化蛋白激酶和核因子κB诱导血管平滑肌细胞中血管细胞黏附分子-1的表达。
Cell Signal. 2007 Oct;19(10):2127-37. doi: 10.1016/j.cellsig.2007.06.009. Epub 2007 Jun 28.
10
Activation of JNK in the inner ear following impulse noise exposure.脉冲噪声暴露后内耳中JNK的激活。
J Neurotrauma. 2008 Jan;25(1):72-7. doi: 10.1089/neu.2007.0346.

引用本文的文献

1
In silico transcriptome screens identify epidermal growth factor receptor inhibitors as therapeutics for noise-induced hearing loss.计算机转录组筛选鉴定表皮生长因子受体抑制剂可作为治疗噪声性听力损失的药物。
Sci Adv. 2024 Jun 21;10(25):eadk2299. doi: 10.1126/sciadv.adk2299. Epub 2024 Jun 19.
2
Differential Expression of miRNAs and Their Predicted Target Pathways in Cochlear Nucleus Following Chronic Noise Exposure in Rats.慢性噪声暴露后大鼠耳蜗核中 miRNAs 的差异表达及其预测靶通路。
Cells. 2022 Jul 22;11(15):2266. doi: 10.3390/cells11152266.
3
Inhibiting DNA methylation alleviates cisplatin-induced hearing loss by decreasing oxidative stress-induced mitochondria-dependent apoptosis the LRP1-PI3K/AKT pathway.
抑制DNA甲基化可通过降低氧化应激诱导的线粒体依赖性凋亡的LRP1-PI3K/AKT途径来减轻顺铂诱导的听力损失。
Acta Pharm Sin B. 2022 Mar;12(3):1305-1321. doi: 10.1016/j.apsb.2021.11.002. Epub 2021 Nov 9.
4
Regulation of Endothelial Nitric Oxide Synthase in the Reticular Lamina of the Organ of Corti by a Nitric Oxide Donor.一氧化氮供体对耳蜗组织的网状层内皮型一氧化氮合酶的调节。
J Histochem Cytochem. 2021 Nov;69(11):731-739. doi: 10.1369/00221554211054642. Epub 2021 Oct 19.
5
Otoprotectants: From Research to Clinical Application.耳保护剂:从研究到临床应用
Semin Hear. 2019 May;40(2):162-176. doi: 10.1055/s-0039-1684045. Epub 2019 Apr 26.
6
Mechanisms of sensorineural cell damage, death and survival in the cochlea.耳蜗中感觉神经细胞损伤、死亡及存活的机制。
Front Aging Neurosci. 2015 Apr 21;7:58. doi: 10.3389/fnagi.2015.00058. eCollection 2015.
7
Application of insulin-like growth factor-1 in the treatment of inner ear disorders.胰岛素样生长因子-1在治疗内耳疾病中的应用。
Front Pharmacol. 2014 Sep 10;5:208. doi: 10.3389/fphar.2014.00208. eCollection 2014.
8
ATP-gated ion channels mediate adaptation to elevated sound levels.ATP 门控离子通道介导适应高音量。
Proc Natl Acad Sci U S A. 2013 Apr 30;110(18):7494-9. doi: 10.1073/pnas.1222295110. Epub 2013 Apr 16.
9
Impact of ozone exposure on prostaglandin release in nasal polyps.臭氧暴露对鼻息肉中前列腺素释放的影响。
Eur Arch Otorhinolaryngol. 2012 Jun;269(6):1623-8. doi: 10.1007/s00405-011-1856-8. Epub 2011 Dec 1.
10
Selective activation of nuclear factor kappa B in the cochlea by sensory and inflammatory stress.感觉和炎症应激对耳蜗中核因子κB的选择性激活。
Neuroscience. 2009 May 5;160(2):530-9. doi: 10.1016/j.neuroscience.2009.02.073. Epub 2009 Mar 11.