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柚皮苷通过多种途径减轻斑马鱼侧线中海因茨素和氨基糖苷类诱导的毛细胞损伤。

Naringin attenuates cisplatin- and aminoglycoside-induced hair cell injury in the zebrafish lateral line via multiple pathways.

机构信息

Department of Clinical Laboratory, Shandong Provincial Hospital, Cheeloo College of Medicine, Shandong University, Jinan, China.

Department of Orthopaedics, Shandong Provincial Hospital, Cheeloo College of Medicine, Shandong University, Jinan, China.

出版信息

J Cell Mol Med. 2021 Jan;25(2):975-989. doi: 10.1111/jcmm.16158. Epub 2020 Dec 3.

Abstract

Exposure to ototoxic drugs is a significant cause of hearing loss that affects about 30 thousand children with potentially serious physical, social and psychological dysfunctions every year. Cisplatin (CP) and aminoglycosides are effective antineoplastic or bactericidal drugs, and their application has a high probability of ototoxicity which results from the death of hair cells (HCs). Here, we describe the therapeutic effect of the flavonoid compound naringin (Nar) against ototoxic effects of cisplatin and aminoglycosides include gentamicin (GM) and neomycin (Neo) in zebrafish HCs. Animals incubated with Nar (100-400 μmol/L) were protected against the pernicious effects of CP (150-250 μmol/L), GM (50-150 μmol/L) and Neo (50-150 μmol/L). We also provide evidence for the potential mechanism of Nar against ototoxicity, including antioxidation, anti-apoptosis, promoting proliferation and hair cell regeneration. We found that mRNA levels of the apoptotic- and pyroptosis-related genes are regulated by Nar both in vivo and in vitro. Finally, by proving that Nar does not affect the anti-tumour efficacy of CP and antibacterial activity of aminoglycosides in vitro, we highlight its value in clinical application. In conclusion, these results unravel a novel therapeutic role for Nar as an otoprotective drug against the adverse effects of CP and aminoglycosides.

摘要

接触耳毒性药物是导致听力损失的一个重要原因,每年约有 3 万名儿童因此受到影响,这些儿童可能存在严重的身体、社交和心理功能障碍。顺铂(CP)和氨基糖苷类是有效的抗肿瘤或杀菌药物,它们的应用具有很高的耳毒性概率,这是由于毛细胞(HCs)死亡所致。在这里,我们描述了黄酮类化合物柚皮苷(Nar)对斑马鱼 HCs 中顺铂和氨基糖苷类(包括庆大霉素(GM)和新霉素(Neo))耳毒性的治疗作用。孵育有 Nar(100-400μmol/L)的动物可以免受 CP(150-250μmol/L)、GM(50-150μmol/L)和 Neo(50-150μmol/L)的有害影响。我们还提供了 Nar 对抗耳毒性的潜在机制的证据,包括抗氧化、抗细胞凋亡、促进增殖和毛细胞再生。我们发现,Nar 体内和体外均可调节与细胞凋亡和细胞焦亡相关的基因的 mRNA 水平。最后,通过证明 Nar 不影响 CP 的抗肿瘤疗效和氨基糖苷类的体外抗菌活性,我们强调了其在临床应用中的价值。总之,这些结果揭示了 Nar 作为一种对抗 CP 和氨基糖苷类不良反应的新型治疗药物的耳保护作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2eaa/7812295/af629512c89c/JCMM-25-975-g001.jpg

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