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Age-associated expression of erythropoietin and its receptor in rat spiral ganglion neurons and its association with neuronal apoptosis and hearing alterations

机译:促红细胞生成素及其受体在大鼠螺旋神经节神经元中的年龄相关表达及其与神经元凋亡和听力改变的关系

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摘要

The present study aimed to determine the expression of erythropoietin (EPO) and the EPO receptor (EPOR) in spiral ganglion neurons (SGNs) in the inner ear of rats of various ages, and the associated neuronal apoptosis and hearing alterations. A total of 15 healthy rats (n=30 ears), were divided into three groups: i) A nominated infant group at post-natal day (PND) 12–14, ii) an adult group at PND 60 and iii) a 3-year postnatal aged group. Auditory brainstem response (ABR) measurements were performed on all rats. EPO and EPOR expression in the inner ear was detected by immunohistochemistry. In situ terminal deoxynucleotidyl transferase dUTP nick end labeling assays were performed to detect the apoptosis of SGNs. The average hearing thresholds of the ABR (decibels above normal hearing level) were 5.625±4.955 in the infant, 15.000±8.498 in the adult and 23.500±13.134 in the aged groups. Hearing thresholds for aged and adult rats increased significantly compared with infant rats. However, the difference in latencies of peak I was not significant (P>0.05). EPO in SGNs was detected during different developmental periods without significant alterations, but were reduced compared with Corti's organ or the stria vascularis. EPOR expression increased significantly from infant to adult stage, and this increased expression was maintained in the aged group. An age-associated increase in the apoptosis of SGNs was detected in all three groups (P=0.0347). The potential neuroprotective effects of EPO in SGNs may not be revealed during the aging process under natural conditions, and may be associated with spontaneous neuronal apoptosis and consequently, hearing diminution. However, the age-associated increase in EPOR in SGNs may exert a role in neuroprotection when necessary, for example in presbycusis.
机译:本研究旨在确定不同年龄大鼠内耳螺旋神经节神经元(SGNs)中促红细胞生成素(EPO)和EPO受体(EPOR)的表达,以及相关的神经元凋亡和听力改变。总共15只健康的大鼠(n = 30耳)分为三组:i)出生后第12-14天的指定婴儿组; ii)60 PND的成年组; iii)a 3岁产后老年组。对所有大鼠进行听性脑干反应(ABR)测量。通过免疫组织化学检测内耳中的EPO和EPOR表达。进行原位末端脱氧核苷酸转移酶dUTP缺口末端标记测定以检测SGN的凋亡。 ABR的平均听力阈值(高于正常听力水平的分贝)在婴儿中为5.625±4.955,在成人中为15.000±8.498,在老年组中为23.500±13.134。与婴儿大鼠相比,老年和成年大鼠的听力阈值显着增加。但是,峰I的潜伏期差异不显着(P> 0.05)。在不同的发育时期检测到SGNs中的EPO没有明显改变,但与Corti器官或血管纹相比有所降低。从婴儿到成年期,EPOR表达均显着增加,并且在老年组中这种表达得以维持。在所有三个组中均检测到了与年龄相关的SGNs凋亡增加(P = 0.0347)。 EPO对SGNs的潜在神经保护作用可能不会在自然条件下的衰老过程中揭示,而可能与自发性神经元凋亡有关,从而导致听力下降。但是,SGN中EPOR的与年龄相关的增加可能在必要时在神经保护中发挥作用,例如在老花眼中。

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