Hu Yue, Ma Xiulan
Department of Otolaryngology Head and Neck Surgery, Shengjing Hospital of China Medical University, Shenyang, China.
Front Pharmacol. 2021 Feb 18;12:620741. doi: 10.3389/fphar.2021.620741. eCollection 2021.
Ototoxicity is a serious health problem that greatly affects millions of people worldwide. This condition is caused by the entry of aminoglycosides into auditory hair cells, subsequently inducing reactive oxygen species (ROS) production and accumulation. Several strategies have been adopted to overcome irreversible ROS-induced hair cell loss in mammals. In recent years, icariin, a major active component of the traditional herb Epimedium, has been widely studied and revealed to have antioxidant, anti-inflammatory, and anti-apoptotic properties. In this study, we found that icariin pretreatment improved the survival rate of gentamicin-treated House Ear Institute-Organ of Corti 1 (HEI-OC1) cells and cochlear explants. Icariin remarkably suppressed HEI-OC1 cell apoptosis and inhibited ROS production in cells. Notably, icariin upregulated PGC-1α (SIRT3 promoter) and SIRT3 expression in HEI-OC1 cells. In addition, SIRT3 inhibition significantly attenuated the anti-apoptotic effect of icariin. We also found that icariin can increase AMPK phosphorylation. Further studies showed that inhibition of SIRT3 activity had no significant effect on AMPK phosphorylation. Furthermore, the AMPK inhibitor compound C significantly suppressed SIRT3 expression, meaning that AMPK, as an upstream molecule, regulates SIRT3 expression. Meanwhile, inhibition of AMPK activity significantly reduced the protective effect of icariin on gentamicin ototoxicity. Based on these results, icariin exerts its protective effect on gentamicin-induced ototoxicity via activation of the AMPK-SIRT3 signaling pathway, thus providing a new strategy for treating ototoxicity caused by aminoglycoside antibiotics.
耳毒性是一个严重的健康问题,极大地影响着全球数百万人。这种情况是由氨基糖苷类药物进入听觉毛细胞引起的,随后诱导活性氧(ROS)的产生和积累。已经采用了几种策略来克服哺乳动物中不可逆的ROS诱导的毛细胞损失。近年来,淫羊藿苷作为传统草药淫羊藿的主要活性成分,已得到广泛研究,并显示具有抗氧化、抗炎和抗凋亡特性。在本研究中,我们发现淫羊藿苷预处理提高了庆大霉素处理的耳科研究所-柯蒂氏器1(HEI-OC1)细胞和耳蜗外植体的存活率。淫羊藿苷显著抑制HEI-OC1细胞凋亡并抑制细胞中的ROS产生。值得注意的是,淫羊藿苷上调了HEI-OC1细胞中PGC-1α(SIRT3启动子)和SIRT3的表达。此外,SIRT3抑制显著减弱了淫羊藿苷的抗凋亡作用。我们还发现淫羊藿苷可以增加AMPK磷酸化。进一步的研究表明,抑制SIRT3活性对AMPK磷酸化没有显著影响。此外,AMPK抑制剂化合物C显著抑制SIRT3表达,这意味着AMPK作为上游分子调节SIRT3表达。同时,抑制AMPK活性显著降低了淫羊藿苷对庆大霉素耳毒性的保护作用。基于这些结果,淫羊藿苷通过激活AMPK-SIRT3信号通路对庆大霉素诱导的耳毒性发挥保护作用,从而为治疗氨基糖苷类抗生素引起的耳毒性提供了一种新策略。