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Folic acid deficiency induces premature hearing loss through mechanisms involving cochlear oxidative stress and impairment of homocysteine metabolism.叶酸缺乏通过耳蜗氧化应激和同型半胱氨酸代谢损伤相关机制诱导听力损失提前发生。
FASEB J. 2015 Feb;29(2):418-32. doi: 10.1096/fj.14-259283. Epub 2014 Nov 10.
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Adenosine kinase: exploitation for therapeutic gain.腺嘌呤激酶:为治疗增益而进行的开发。
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Adenosine kinase inhibition in the cochlea delays the onset of age-related hearing loss.耳蜗中的腺苷激酶抑制可延缓与年龄相关的听力损失的发生。
Exp Gerontol. 2011 Nov;46(11):905-14. doi: 10.1016/j.exger.2011.08.001. Epub 2011 Aug 7.

本文引用的文献

1
Adenosine amine congener mitigates noise-induced cochlear injury.腺苷胺同系物减轻噪声诱导的耳蜗损伤。
Purinergic Signal. 2010 Jun;6(2):273-81. doi: 10.1007/s11302-010-9188-5. Epub 2010 Jun 30.
2
Distribution of NTPDase5 and NTPDase6 and the regulation of P2Y receptor signalling in the rat cochlea.NTPDase5 和 NTPDase6 在大鼠耳蜗中的分布及其对 P2Y 受体信号转导的调节。
Purinergic Signal. 2010 Jun;6(2):249-61. doi: 10.1007/s11302-010-9190-y. Epub 2010 Jun 19.
3
Differential expression of P2Y receptors in the rat cochlea during development.在发育过程中大鼠耳蜗中 P2Y 受体的差异表达。
Purinergic Signal. 2010 Jun;6(2):231-48. doi: 10.1007/s11302-010-9191-x. Epub 2010 Jun 11.
4
Developmentally regulated expression of ectonucleotidases NTPDase5 and NTPDase6 and UDP-responsive P2Y receptors in the rat cochlea.发育调控的核苷酸酶 NTPDase5 和 NTPDase6 以及 UDP 反应性 P2Y 受体在大鼠耳蜗中的表达。
Histochem Cell Biol. 2010 Apr;133(4):425-36. doi: 10.1007/s00418-010-0682-1. Epub 2010 Mar 10.
5
Post exposure administration of A(1) adenosine receptor agonists attenuates noise-induced hearing loss.暴露后给予 A(1) 腺苷受体激动剂可减轻噪声性听力损失。
Hear Res. 2010 Feb;260(1-2):81-8. doi: 10.1016/j.heares.2009.12.004. Epub 2009 Dec 6.
6
Purinergic signaling in special senses.特殊感觉中的嘌呤能信号传导。
Trends Neurosci. 2009 Mar;32(3):128-41. doi: 10.1016/j.tins.2009.01.001. Epub 2009 Feb 18.
7
Adenosine kinase is a target for the prediction and prevention of epileptogenesis in mice.腺苷激酶是预测和预防小鼠癫痫发生的一个靶点。
J Clin Invest. 2008 Feb;118(2):571-82. doi: 10.1172/JCI33737.
8
Adenosine as a neuromodulator in neurological diseases.腺苷作为神经疾病中的一种神经调质
Curr Opin Pharmacol. 2008 Feb;8(1):2-7. doi: 10.1016/j.coph.2007.09.002. Epub 2007 Oct 17.
9
KCNQ1/KCNE1 K+ channel and P2Y4 receptor are co-expressed from the time of birth in the apical membrane of rat strial marginal cells.KCNQ1/KCNE1钾通道和P2Y4受体在大鼠螺旋韧带边缘细胞顶端膜从出生时起就共同表达。
Acta Otolaryngol Suppl. 2007 Oct(558):30-5. doi: 10.1080/03655230701624830.
10
Spatiotemporal definition of neurite outgrowth, refinement and retraction in the developing mouse cochlea.发育中小鼠耳蜗中神经突生长、细化和回缩的时空定义。
Development. 2007 Aug;134(16):2925-33. doi: 10.1242/dev.001925. Epub 2007 Jul 11.

腺苷激酶在耳蜗发育和对噪声反应中的作用。

Role of adenosine kinase in cochlear development and response to noise.

机构信息

Department of Physiology, Faculty of Medical and Health Sciences, The University of Auckland, Aukland, New Zealand.

出版信息

J Neurosci Res. 2010 Sep;88(12):2598-609. doi: 10.1002/jnr.22421.

DOI:10.1002/jnr.22421
PMID:20648650
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3041170/
Abstract

Adenosine signalling has an important role in cochlear protection from oxidative stress. In most tissues, intracellular adenosine kinase (ADK) is the primary route of adenosine metabolism and the key regulator of intracellular and extracellular adenosine levels. The present study provides the first evidence for ADK distribution in the adult and developing rat cochlea. In the adult cochlea, ADK was localized to the nuclear or perinuclear region of spiral ganglion neurons, lateral wall tissues, and epithelial cells lining scala media. In the developing cochlea, ADK was strongly expressed in multiple cell types at birth and reached its peak level of expression at postnatal day 21 (P21). Ontogenetic changes in ADK expression were evident in the spiral ganglion, organ of Corti, and stria vascularis. In the spiral ganglion, ADK showed a shift from predominantly satellite cell immunolabelling at P1 to neuronal expression from P14 onward. In contrast to the role of ADK in various aspects of cochlear development, the ADK contribution to the cochlear response to noise stress was less obvious. Transcript and protein levels of ADK were unaltered in the cochlea exposed to broadband noise (90-110 dBSPL, 24 hr), and the selective inhibition of ADK in the cochlea with ABT-702 failed to restore hearing thresholds after exposure to traumatic noise. This study indicates that ADK is involved in purine salvage pathways for nucleotide synthesis in the adult cochlea, but its role in the regulation of adenosine signalling under physiological and pathological conditions has yet to be established.

摘要

腺苷信号在耳蜗免受氧化应激的保护中具有重要作用。在大多数组织中,细胞内腺苷激酶(ADK)是腺苷代谢的主要途径,也是细胞内和细胞外腺苷水平的关键调节剂。本研究首次提供了 ADK 在成年和发育中的大鼠耳蜗中的分布证据。在成年耳蜗中,ADK 定位于螺旋神经节神经元的核或核周区域、侧壁组织和衬里中阶的上皮细胞。在发育中的耳蜗中,ADK 在出生时强烈表达于多种细胞类型,并在出生后第 21 天(P21)达到表达高峰。ADK 表达的个体发育变化在螺旋神经节、柯蒂氏器和血管纹中显而易见。在螺旋神经节中,ADK 从 P1 时主要定位于卫星细胞免疫标记转变为 P14 以后的神经元表达。与 ADK 在耳蜗发育各个方面的作用相反,ADK 对耳蜗对噪声应激的反应的贡献不太明显。暴露于宽带噪声(90-110dBSPL,24 小时)后,耳蜗中的 ADK 转录本和蛋白水平没有改变,并且用 ABT-702 选择性抑制耳蜗中的 ADK 也未能在暴露于创伤性噪声后恢复听力阈值。本研究表明,ADK 参与成年耳蜗中核苷酸合成的嘌呤补救途径,但它在生理和病理条件下调节腺苷信号的作用尚未确定。