[Establishment of model with inner ear mimetic aging and mtDNA 4834 bp deletion in rats].

Weijia Kong, Yujuan Hu, Qiong Wang, Li Xu, Ying Wang, Yuechen Han, Jun Li, Bo Liu, Wen Kong
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Abstract

Objective: To explore the establishment of the mimetic aging effect in the inner ear of the rat.

Method: Twenty-four Wistar rats were randomly divided into two groups: group A (D-galactose group, n = 14), which were treated with hypodermic 5% D-galactose (150 mg x kg(-1) x d(-1)) for 8 weeks and then with intraperitoneal saline for 10 days, and group B (control group, n = 10), which were given saline only. Auditory brainstem response(ABR) was used to detect the hearing threshold of rats, and colorimetry was used to analyze the activity of the glutathione peroxidase (GSH-PX). The inner ear tissue was harvested and mitochondrial DNA was amplified to identify the 4 834 bp deletion mutation by nested primer polymerase chain reaction (nested PCR) technique.

Result: The incidence of mitochondrial DNA 4 834 bp deletion of group A was 100% (28/28), while the deletion of group B was 0. The activity of the GSH-PX in group A (59.07 +/- 8.70 U) was lower than that in group B (142.10 +/- 7.02 U). The difference between group A and group B was significant (t-test, P < 0.01). Variation in ABR threshold of (5.36 +/- 3.08) dB peSPL was observed in group A, and (6.50 +/- 3.37) dB peSPL in group B. The difference in shift of ABR threshold between group A and group B was not significant (P > 0.05).

Conclusion: The mimetic aging effect in the inner ear of the rat can be induced by D-galactose, and this rat model presents high incidence of mtDNA4834 deletion. But no hearing loss was found in this model.

[大鼠内耳模拟衰老及mtDNA 4834 bp缺失模型的建立]。
目的:探讨大鼠内耳模拟衰老效应的建立。方法:将24只Wistar大鼠随机分为两组:A组(d -半乳糖组,n = 14),给予5% d -半乳糖(150 mg x kg(-1) x d(-1))皮下注射8周,然后腹腔注射生理盐水10 d; B组(对照组,n = 10),只给予生理盐水。用听觉脑干反应(ABR)检测大鼠的听阈,用比色法分析谷胱甘肽过氧化物酶(GSH-PX)活性。采集内耳组织,扩增线粒体DNA,采用巢式引物聚合酶链反应(巢式PCR)技术鉴定4 834 bp缺失突变。结果:A组线粒体DNA 4 834 bp缺失发生率为100% (28/28),B组为0。A组GSH-PX活性(59.07 +/- 8.70 U)低于B组(142.10 +/- 7.02 U),两组间差异有统计学意义(t检验,P < 0.01)。A组ABR阈值变化为(5.36 +/- 3.08)dB peSPL, B组为(6.50 +/- 3.37)dB peSPL, A组与B组ABR阈值变化无显著性差异(P > 0.05)。结论:d -半乳糖可诱导大鼠内耳模拟衰老,且该模型大鼠mtDNA4834缺失发生率高。但在这个模型中没有发现听力损失。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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