Department of Otolaryngology, Head and Neck Surgery, Graduate School of Comprehensive Human Sciences, University of Tsukuba, 1-1-1 Tennodai, Tsukuba 305-8575, Japan.
Neuroscience. 2010 Mar 17;166(2):665-70. doi: 10.1016/j.neuroscience.2009.12.038. Epub 2009 Dec 30.
This study evaluated the protective role of p38 mitogen-activated protein kinase (p38 MAPK) inhibitors and sequestosome 1 (Sqstm1/A170/p62), a stress-induced signal modulator, in acoustic injury of the cochlea in mice. Two weeks after the exposure of mice to acoustic stress, threshold shifts of the auditory brainstem response (ABR) from the pre-exposure level and hair cell loss were evaluated. The activation of p38 MAPK was observed in cochlea by immunostaining 4 h after acoustic stress. To examine the role of p38 MAPK in tissue injury, its inhibitors were i.p. injected into male wild-type C57BL mice before the acoustic overexposure. The inhibitors SB202190 and SB203580 but not the inactive analogue SB202474 dose-dependently decreased the auditory threshold shift and outer hair cell loss induced by acoustic overexposure, suggesting the involvement of p38 MAPK in ototoxicity. We found that acoustic overexposure induced the up-regulation of Sqstm1 mRNA expression in the cochlea of wild-type mice and that SQSTM1-deficient mice exhibited an enhanced ABR threshold shift and hair cell loss, suggesting a role of SQSTM1 in the protection of tissue from acoustic stress.
本研究评估了 p38 丝裂原活化蛋白激酶 (p38 MAPK) 抑制剂和自噬相关蛋白 1 (Sqstm1/A170/p62) 在小鼠耳蜗声损伤中的保护作用。声应激暴露小鼠 2 周后,评估听觉脑干反应 (ABR) 阈值相对于暴露前的偏移和毛细胞损失。声应激后 4 小时通过免疫染色观察到耳蜗中 p38 MAPK 的激活。为了研究 p38 MAPK 在组织损伤中的作用,在雄性野生型 C57BL 小鼠进行声过度暴露前,通过腹腔注射其抑制剂 SB202190 和 SB203580,但不是非活性类似物 SB202474,剂量依赖性地降低了由声过度暴露引起的听觉阈值偏移和外毛细胞损失,表明 p38 MAPK 参与了耳毒性。我们发现,声过度暴露诱导野生型小鼠耳蜗中 Sqstm1 mRNA 表达的上调,并且 SQSTM1 缺陷型小鼠表现出 ABR 阈值偏移和毛细胞损失增强,表明 SQSTM1 在组织对抗声应激中起保护作用。