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中枢突损伤后听觉神经元的凋亡

Apoptosis of auditory neurons following central process injury.

作者信息

Sekiya Tetsuji, Yagihashi Akinori, Shimamura Norihito, Asano Kenichiro, Suzuki Shigeharu, Matsubara Atsushi, Namba Atsushi, Shinkawa Hideichi

机构信息

Neurosurgery Department, Hirosaki University School of Medicine, Hirosaki 036-8216, Japan.

出版信息

Exp Neurol. 2003 Dec;184(2):648-58. doi: 10.1016/S0014-4886(03)00288-7.

Abstract

Although apoptotic changes in auditory neurons induced by injury to peripheral processes (dendrites) have been intensively studied, apoptotic changes in auditory neurons induced by injury to central processes (axons of spiral ganglion cells, SGCs) have not been reported previously, probably due to lack of an experimental model. The present study reports for the first time the appearance, extent, and time course of SGC apoptosis following injury to the central processes. Apoptosis was studied in a rat model that consisted of compression of the auditory nerve in the cerebellopontine (CP) angle cistern with intraoperative recordings of auditory nerve compound action potentials (CAPs) to ensure highly reproducible results. Rats were killed between day 0 and day 14 after compression and apoptosis of SGCs was evaluated quantitatively as well as qualitatively by terminal deoxynucleotidyl transferase (TdT)-mediated deoxyuridine triphosphate nick-end labeling (TUNEL) staining, anti-activated caspase-3 immunostaining, Hoechst 33342 staining, and electron microscopy. The average number of TUNEL-positive apoptotic SGCs in each cochlear turn increased from day 1 to day 5 and then decreased gradually to an undetectable level on day 14 after compression. The average proportion of apoptotic SGCs identified in any cochlear turn on any day was always lower than 10%. The results of our present study should be useful in determining the therapeutic time window for rescuing auditory neurons undergoing apoptosis due to injury during surgery in the CP angle.

摘要

尽管对外周突(树突)损伤诱导的听觉神经元凋亡变化已进行了深入研究,但中枢突(螺旋神经节细胞,SGCs的轴突)损伤诱导的听觉神经元凋亡变化此前尚未见报道,这可能是由于缺乏实验模型。本研究首次报道了中枢突损伤后SGCs凋亡的出现、程度和时间进程。在一个大鼠模型中研究凋亡情况,该模型通过在小脑脑桥(CP)角池压迫听神经,并术中记录听神经复合动作电位(CAPs),以确保结果具有高度可重复性。在压迫后0至14天之间处死大鼠,通过末端脱氧核苷酸转移酶(TdT)介导的脱氧尿苷三磷酸缺口末端标记(TUNEL)染色、抗活化半胱天冬酶-3免疫染色、Hoechst 33342染色和电子显微镜对SGCs的凋亡进行定量和定性评估。每个耳蜗转中TUNEL阳性凋亡SGCs的平均数量从压迫后第1天到第5天增加,然后在第14天逐渐下降到不可检测水平。在任何一天的任何耳蜗转中鉴定出的凋亡SGCs的平均比例始终低于10%。我们目前的研究结果对于确定在CP角手术期间因损伤而正在经历凋亡的听觉神经元的治疗时间窗应该是有用的。

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