Rutin Attenuates Gentamycin-induced Hair Cell Injury in the Zebrafish Lateral Line via Suppressing STAT1

• Published in: Molecular neurobiology Vol. 61; no. 11; pp. 9548 - 9561
• Main Authors: Yang, Huiming, Zong, Tao, Liu, Jing, Wang, Dengxu, Gong, Ke, Yin, Haiyan, Zhang, Weiwei, Xu, Tong, Yang, Rong
• Format: Journal Article
• Language: English
• Published: New York Springer US 01.11.2024; Springer Nature B.V
• Subjects: Aminoglycoside antibiotics; Antibiotics; Antibodies; Apoptosis; Bacteriostats; Biomedical and Life Sciences; Biomedicine; Cell Biology; Cell death; Cell injury; Cell proliferation; Clinical medicine; Danio rerio; Diabetes; Drugs; Flavonoids; Gentamicin; Gram-negative bacteria; Hair; Hair cells; Hearing loss; Hearing protection; Lateral line; Necroptosis; Neurobiology; Neurology; Neuromasts; Neurosciences; Otolaryngology; Ototoxicity; Oxidation; Proteomics; Reactive oxygen species; Rutin; Stat1 protein; Toxicity; Zebrafish; Zebrafish; Otoprotective drug; Rutin; Gentamicin; Hair cells
• ISSN: 0893-7648; 1559-1182; 1559-1182
• DOI: 10.1007/s12035-024-04179-4

Aminoglycoside antibiotics, including gentamicin (GM), induce delayed ototoxic effects such as hearing loss after prolonged use, which results from the death of hair cells. However, the mechanisms underlying the ototoxicity of aminoglycosides warrant further investigation, and there are currently no effective drugs in the clinical setting. Herein, the therapeutic effect of the flavonoid compound rutin against the ototoxic effects of GM in zebrafish hair cells was investigated. Animals incubated with rutin (100–400 µmol/L) were protected against the pernicious effects of GM (200 µmol/L). We found that rutin improves hearing behavior in zebrafish, and rutin was effective in reducing the number of Tunel-positive cells in the neuromasts of the zebrafish lateral line and promoting cell proliferation after exposure to GM. Subsequently, rutin exerted a protective effect against GM-induced cell death in HEI-OC1 cells and could limit the production of cytosolic reactive oxygen species (ROS) and diminish the percentage of apoptotic cells. Additionally, the results of the proteomic analysis revealed that rutin could effectively inhibit the expression of necroptosis and apoptosis related genes. Meanwhile, molecular docking analysis revealed a high linking activity between the molecular docking of rutin and STAT1 proteins. The protection of zebrafish hair cells or HEI-OC1 cells from GM-induced ototoxicity by rutin was attenuated by the introduction of STAT1 activator. Finally, we demonstrated that rutin significantly improves the bacteriostatic effect of GM by in vitro experiments, emphasising its clinical application value. In summary, these results collectively unravel a novel therapeutic role for rutin as an otoprotective drug against the adverse effects of GM.