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Mechanisms and otoprotective strategies of programmed cell death on aminoglycoside-induced ototoxicity.
Han, Lei; Wang, Zijing; Wang, Daqi; Gao, Ziwen; Hu, Shaowei; Shi, Dazhi; Shu, Yilai.
Afiliação
  • Han L; Department of Otorhinolaryngology, The Second Affiliated Hospital, Hengyang Medical School, University of South China, Hengyang, China.
  • Wang Z; ENT Institute and Department of Otorhinolaryngology, Eye and ENT Hospital, State Key Laboratory of Medical Neurobiology and MOE Frontiers Center for Brain Science, Fudan University, Shanghai, China.
  • Wang D; Institutes of Biomedical Sciences, Fudan University, Shanghai, China.
  • Gao Z; NHC Key Laboratory of Hearing Medicine, Fudan University, Shanghai, China.
  • Hu S; Department of Otorhinolaryngology, The Second Affiliated Hospital, Hengyang Medical School, University of South China, Hengyang, China.
  • Shi D; ENT Institute and Department of Otorhinolaryngology, Eye and ENT Hospital, State Key Laboratory of Medical Neurobiology and MOE Frontiers Center for Brain Science, Fudan University, Shanghai, China.
  • Shu Y; Institutes of Biomedical Sciences, Fudan University, Shanghai, China.
Front Cell Dev Biol ; 11: 1305433, 2023.
Article em En | MEDLINE | ID: mdl-38259515
ABSTRACT
Aminoglycosides are commonly used for the treatment of life-threatening bacterial infections, however, aminoglycosides may cause irreversible hearing loss with a long-term clinical therapy. The mechanism and prevention of the ototoxicity of aminoglycosides are still limited although amounts of studies explored widely. Specifically, advancements in programmed cell death (PCD) provide more new perspectives. This review summarizes the general signal pathways in programmed cell death, including apoptosis, autophagy, and ferroptosis, as well as the mechanisms of aminoglycoside-induced ototoxicity. Additionally, novel interventions, especially gene therapy strategies, are also investigated for the prevention or treatment of aminoglycoside-induced hearing loss with prospective clinical applications.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Front Cell Dev Biol Ano de publicação: 2023 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Front Cell Dev Biol Ano de publicação: 2023 Tipo de documento: Article País de afiliação: China