Inhibition of the mitochondrial permeability transition pore as a promising target for protecting auditory function in cisplatin-induced hearing loss

Ye Ri Kim, Sujin Jun, Sunhwa Jung, Byeonghyeon Lee, Sang Hee Lee, Jaehyuk Lee, Jong Su Hwang, Themis Thoudam, Hoyul Lee, Ibotombi Singh Sinam, Jae Han Jeon, Kyu Yup Lee, Sun Joon Min, Un Kyung Kim

Research output: Contribution to journalArticlepeer-review

Abstract

mPTP is a multi-protein complex that opens in mitochondria during cell death. Cisplatin-induced hearing loss is also known to be caused by mPTP opening. Thus, our study evaluated the protective effect of a novel mPTP inhibitor named DBP-iPT against cisplatin-induced hearing loss. The cell viability result showed that DBP-iPT provided a 40 % protective effect compared to the group treated with cisplatin. In addition, the DBP-iPT treated group exhibited a reduction in intracellular ROS levels, counteracting the excessive ROS accumulation induced by cisplatin at the whole cell level. Intriguingly, mitochondrial ROS levels in the DBP-iPT group were elevated three-fold compared to the cisplatin-treated group. Despite this increase in mitochondrial ROS, the mitochondrial membrane potential in the DBP-iPT group was three times higher than that of the control. These findings present intriguing contradictions to prior studies. Therefore, we investigated whether the mitochondria were damaged or not and found that DBP-iPT treatment maintained an increased portion of elongated mitochondria, suggesting autophagy-mediated removal of damaged mitochondria. This process leads to improved mitochondrial dynamics. Finally, in vivo studies confirmed that the ABR test using a mouse model showed the same pattern of protection against cisplatin-induced hearing loss in the DBP-iPT treatment group. We have identified a new target that has a protective effect against cisplatin-induced hearing loss. Therefore, this study is expected to provide valuable insights as it focuses on targeting mPTP opening to protect against ototoxicity caused by cisplatin. This discovery will serve as a significant foundation for future research.

Original languageEnglish
Article number117767
JournalBiomedicine and Pharmacotherapy
Volume182
DOIs
StatePublished - Jan 2025

Keywords

  • Autophagy
  • Cisplatin
  • Hearing loss
  • Mitochondrial permeability transition pore
  • Reactive oxygen species

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