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Corticosteroid therapy for hearing and balance disorders.皮质类固醇治疗听力和平衡障碍。
Anat Rec (Hoboken). 2012 Nov;295(11):1928-43. doi: 10.1002/ar.22576. Epub 2012 Oct 8.
2
Oxidative stress, inflammation, and autophagic stress as the key mechanisms of premature age-related hearing loss in SAMP8 mouse Cochlea.氧化应激、炎症和自噬应激作为 SAMP8 小鼠耳蜗衰老性听力损失的关键机制。
Antioxid Redox Signal. 2012 Feb 1;16(3):263-74. doi: 10.1089/ars.2011.4037. Epub 2011 Dec 1.
3
Tissue remodeling in the acute otitis media mouse model.急性中耳炎小鼠模型中的组织重塑
Int J Pediatr Otorhinolaryngol. 2011 Nov;75(11):1368-71. doi: 10.1016/j.ijporl.2011.07.026. Epub 2011 Sep 1.
4
Control of chronic otitis media and sensorineural hearing loss in C3H/HeJ mice: glucocorticoids vs mineralocorticoids.C3H/HeJ小鼠慢性中耳炎和感音神经性听力损失的控制:糖皮质激素与盐皮质激素的比较
Otolaryngol Head Neck Surg. 2008 Nov;139(5):646-53. doi: 10.1016/j.otohns.2008.07.029.
5
Stepwise replication identifies a low-producing lymphotoxin-alpha allele as a major risk factor for early-onset leprosy.逐步复制法确定低产淋巴毒素-α等位基因是早发型麻风病的主要危险因素。
Nat Genet. 2007 Apr;39(4):517-22. doi: 10.1038/ng2000. Epub 2007 Mar 11.
6
Age-related hearing loss in CD/1 mice is associated to ROS formation and HIF target proteins up-regulation in the cochlea.CD/1小鼠的年龄相关性听力损失与耳蜗中活性氧的形成及低氧诱导因子靶蛋白的上调有关。
Exp Gerontol. 2007 Apr;42(4):327-36. doi: 10.1016/j.exger.2006.10.014. Epub 2006 Dec 4.
7
Impaired skeletal development in interleukin-6-transgenic mice: a model for the impact of chronic inflammation on the growing skeletal system.白细胞介素-6转基因小鼠骨骼发育受损:慢性炎症对生长中骨骼系统影响的模型
Arthritis Rheum. 2006 Nov;54(11):3551-63. doi: 10.1002/art.22175.
8
Intratympanic injection of dexamethasone: time course of inner ear distribution and conversion to its active form.鼓室内注射地塞米松:内耳分布的时间进程及其向活性形式的转化。
Otol Neurotol. 2006 Jun;27(4):564-9. doi: 10.1097/01.mao.0000194814.07674.4f.
9
Apical-to-basal gradients in age-related cochlear degeneration and their relationship to "primary" loss of cochlear neurons.年龄相关性耳蜗退变中的顶-底梯度及其与耳蜗神经元“原发性”丢失的关系。
J Comp Neurol. 2004 Nov 1;479(1):103-16. doi: 10.1002/cne.20326.
10
Mineralocorticoid receptor-mediated inhibition of the hypothalamic-pituitary-adrenal axis in aged humans.盐皮质激素受体介导的老年人下丘脑-垂体-肾上腺轴抑制
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BALB/cJ小鼠全身与鼓室内给予类固醇药物后与年龄相关的耳蜗细胞因子基因表达

Age-related cochlear cytokine gene expression in the BALB/cJ mouse with systemic versus intratympanic dosing of steroid drugs.

作者信息

Tokarz Sara A, Pang Jiaqing, Grosz Anna, Kempton J Beth, Trune Dennis R, Pillers De-Ann M

机构信息

Division of Neonatology, Department of Pediatrics, University of Wisconsin-Madison, Meriter Hospital, Madison, WI 53715, USA.

出版信息

Acta Otolaryngol. 2013 Jul;133(7):685-91. doi: 10.3109/00016489.2013.771407.

DOI:10.3109/00016489.2013.771407
PMID:23768053
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3968830/
Abstract

CONCLUSION

Age-related differences in the expression of inflammatory cytokines in the inner ear may contribute to the development of age-related hearing loss (ARHL).

OBJECTIVES

ARHL is characterized by tissue remodeling, ischemia, ion homeostasis, and inflammation. Steroid therapy is an otoprotective strategy that likely acts by reducing inflammation. We examined age-related changes in cytokine gene expression in the cochlea of the BALB/cJ mouse model of premature ARHL after systemic or intratympanic steroid delivery.

METHODS

'Young' (2.5-3 months) and 'Old' (5-9 months) mice were treated with dexamethasone or fludrocortisone administered either orally or intratympanically. Cytokine gene expression in cochlear RNA was analyzed using prefabricated cDNA arrays. Old groups were compared to Young groups to identify age-related changes.

RESULTS

Down-regulation of a cytokine associated with bone remodeling (SPP1) was observed in the untreated Old group. Numerous genes were up- or down-regulated by more than twofold by steroid treatment, including proinflammatory interleukins (IL-16) and anti-inflammatory cytokines.

摘要

结论

内耳中炎症细胞因子表达的年龄相关性差异可能促成年龄相关性听力损失(ARHL)的发生。

目的

ARHL的特征为组织重塑、缺血、离子稳态及炎症。类固醇疗法是一种耳保护策略,可能通过减轻炎症起作用。我们研究了在全身或鼓室内给予类固醇后,过早发生ARHL的BALB/cJ小鼠模型耳蜗中细胞因子基因表达的年龄相关性变化。

方法

“年轻”(2.5 - 3个月)和“年老”(5 - 9个月)小鼠接受口服或鼓室内给予地塞米松或氟氢可的松治疗。使用预制的cDNA阵列分析耳蜗RNA中的细胞因子基因表达。将老年组与年轻组进行比较,以确定年龄相关性变化。

结果

在未治疗的老年组中观察到与骨重塑相关的细胞因子(SPP1)下调。类固醇治疗使众多基因上调或下调超过两倍,包括促炎白细胞介素(IL - 16)和抗炎细胞因子。