20(S)-Ginsenoside Rh1 inhibits cisplatin-induced hearing loss by inhibiting the MAPK signaling pathway and suppressing apoptosis in vitro
Author:
Funder
National Natural Science Foundation of China
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology
Reference48 articles.
1. Aminoglycoside- and cisplatin-induced ototoxicity: mechanisms and otoprotective strategies;Kros;Cold Spring Harb. Perspect. Med.,2019
2. Cisplatin is retained in the cochlea indefinitely following chemotherapy;Breglio;Nat. Commun.,2017
3. Mechanisms of cisplatin-induced ototoxicity and otoprotection;Sheth;Front. Cell. Neurosci.,2017
4. Cisplatin-induced ototoxicity: effects,mechanisms and protection strategies;Callejo;Toxics,2015
5. Knockdown and mutation of Pou4f3 gene mutation promotes pyroptosis of cochleae in cisplatin-induced deafness mice by NLRP3/caspase-3/GSDME pathway;Yu;Toxicology,2022
Cited by 3 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. 20(S)-Ginsenoside Rh1 alleviates sevoflurane-induced ototoxicity by reducing oxidative stress levels;NeuroReport;2023-12-22
2. KSR1 knockout mouse model demonstrates MAPK pathway’s key role in cisplatin- and noise-induced hearing loss;2023-11-13
3. 3,5,6-Trichloro-2-pyridinol confirms ototoxicity in mouse cochlear organotypic cultures and induces cytotoxicity in HEI-OC1 cells;Toxicology and Applied Pharmacology;2023-09
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