Hydrogen peroxide toxicity on auditory cells: An in vitro study

In recent decades, interest has increased in the role of reactive oxygen species (ROS) in health and disease. The ROS are key causative factors in several hearing loss pathologies including ototoxicity, noise trauma, cochlear ageing and ischemic injury. In order to investigate ROS effects on inner ear cells and counteract them, we developed an in vitro model of oxidative stress by exposing the inner ear cell line OC-k3 to hydrogen peroxide (H2O2) at concentrations able to affect in vivo cellular components but allowing cell survival. The treatment with high concentrations (20 and 30 mu M) resulted in reduction of cell viability, activation of apoptosis/necrosis and alteration of morphology, cell cycle progression and antioxidant defences. The ROS effects in inner ear cells are difficult to assess in vivo. Organocultures may provide preservation of tissue architecture but involve ethical issues and can be used only for a limited time. An in vitro model that could be commercially available and easy to handle is necessary to investigate inner ear oxidative stress and the ways to counteract it. The OC-k3 line is a suitable in vitro model to study ROS effects on inner ear cells because the observed cell alterations and damages were similar to those reported in studies investigating ROS effects of ototoxic drugs, noise trauma and cochlear ageing.

Automated summary

The study highlights the importance of reactive oxygen species (ROS) in hearing loss pathologies and the development of an in vitro model using the OC-k3 cell line to study the effects of ROS on inner ear cells. High concentrations of hydrogen peroxide resulted in reduced cell viability, activation of apoptosis/necrosis, and alteration of cell morphology, cell cycle progression, and antioxidant defenses. This model could be valuable for investigating inner ear oxidative stress and potential countermeasures.