The Role and Research Progress of Mitochondria in Sensorineural Hearing Loss

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Abstract

Hearing loss is one of the most common human diseases, seriously affecting everyday lives. Mitochondria, as the energy metabolism center in cells, are also involved in regulating active oxygen metabolism and mediating the occurrence of inflammation and apoptosis. Mitochondrial defects are closely related to hearing diseases. Studies have shown that mitochondrial DNA mutations are one of the causes of hereditary hearing loss. In addition, changes in mitochondrial homeostasis are directly related to noise-induced hearing loss and presbycusis. This review mainly summarizes and discusses the effects of mitochondrial dysfunction and mitophagy on hearing loss. Subsequently, we introduce the recent research progress of targeted mitochondria therapy in the hearing system.

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Xu, S., & Yang, N. (2025, June 1). The Role and Research Progress of Mitochondria in Sensorineural Hearing Loss. Molecular Neurobiology. Springer. https://doi.org/10.1007/s12035-024-04470-4

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