Xu Li, Hu Yujuan, Kong Weijia, Shi Hong, Peng Wei, Hu Yuan
Department of Otolaryngology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430022, China.
Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2010 Oct;24(19):895-8, 900.
Use the inner ear mimetic aging model which has been established by our research institute, investigate its sensitivity to noise trauma and the possible role of mitochondrial DNA deletions.
Thirty-two Wistar rats of 2 months old were randomly divided into four groups. In group A, D-galactose was subcutaneously injected at dose of 150 mg/kg weigh per day for 8 weeks, after that these rats were exposed to 110 dB SPL noise 4 hours each day, for 2 days. Group B were given normal saline (NS) injected at dose of 150 mg/kg weigh per day for 8 weeks,also given noise exposure as that of group A. Group C were give D-galactose without noise exposure. Group D were given normal saline (NS) without noise exposure. The thresholds of auditory brainstem response (ABR) were measured 2 weeks after stopping of noise exposure. And T-SOD and MDA of the inner membranous labyrinthine tissue were measured. Nest polymerase chain reaction (Nest PCR) were used to identify the mtDNA common deletion (CD), and PCR products were sequenced in the meantime.
The elevation of the mean ABR thresholds in group A was higher than that in group B, and the difference had statistic significance (P < 0.01). The reduction of T-SOD in group A was obvious, while the level of MDA was greatly increased. The difference in the levels of T-SOD and MDA between group A and group B had statistic significance (P < 0.01). The detection rate of mtDNA 4834 deletion were as follows: group A 87.5% (7/8); group B 12.5% (1/8); group C 75.0% (1/8); group D 0(0/8).
The rat in the inner ear mimetic aging model are hypersensitive to noise exposure, and mtDNA4834 deletions in the inner ear may play an important role in it.
利用本研究所建立的内耳拟衰老模型,研究其对噪声损伤的敏感性以及线粒体DNA缺失可能发挥的作用。
将32只2月龄Wistar大鼠随机分为四组。A组大鼠每天皮下注射150mg/kg体重的D-半乳糖,连续8周,之后每天暴露于110dB SPL噪声中4小时,共2天。B组大鼠每天皮下注射150mg/kg体重的生理盐水,连续8周,同样给予与A组相同的噪声暴露。C组大鼠给予D-半乳糖但不进行噪声暴露。D组大鼠给予生理盐水且不进行噪声暴露。在停止噪声暴露2周后测量听性脑干反应(ABR)阈值。并测量内耳膜迷路组织的T-SOD和MDA。采用巢式聚合酶链反应(Nest PCR)鉴定线粒体DNA常见缺失(CD),同时对PCR产物进行测序。
A组平均ABR阈值升高幅度高于B组,差异具有统计学意义(P<0.01)。A组T-SOD降低明显,而MDA水平大幅升高。A组与B组T-SOD和MDA水平差异具有统计学意义(P<0.01)。线粒体DNA 4834缺失的检出率如下:A组87.5%(7/8);B组12.5%(1/8);C组75.0%(1/8);D组0(0/8)。
内耳拟衰老模型大鼠对噪声暴露敏感,内耳中的线粒体DNA4834缺失可能在其中起重要作用。