Cochlear implantation trauma and noise-induced hearing loss: Apoptosis and therapeutic strategies
- PMID: 16550592
- DOI: 10.1002/ar.a.20305
Cochlear implantation trauma and noise-induced hearing loss: Apoptosis and therapeutic strategies
Abstract
Cochlear implantation trauma and noise-induced hearing loss both involve a physical disruption of the organ of Corti and may involve several mechanisms of cell death at the molecular level, i.e., necrosis, necrosis-like programmed cell death (PCD; type 2 PCD), and apoptosis (type 1 PCD). This article reviews several promising therapeutic strategies that are currently being developed. One of these promising new strategies involves the use of a highly effective peptide inhibitor of the c-Jun N-terminal kinase cell death signal cascade (i.e., D-JNKI-1) to prevent apoptosis of injured auditory hair cells. Our recent studies showed prevention of cochlear implantation-induced hearing loss by infusing this peptide into the cochlea of guinea pigs. Another otoprotective therapy under investigation is the application of mild hypothermia to protect the cochlea from the development of a hearing loss that follows exposure to a physical trauma, e.g., electrode array insertional trauma. These forward-looking strategies have the potential of improving hearing outcomes after cochlear implantation and providing novel means of otoprotection from noise-induced trauma.
Copyright 2006 Wiley-Liss, Inc.
Similar articles
-
D-JNKI-1 treatment prevents the progression of hearing loss in a model of cochlear implantation trauma.Otol Neurotol. 2006 Jun;27(4):504-11. doi: 10.1097/01.mao.0000217354.88710.13. Otol Neurotol. 2006. PMID: 16791042
-
A peptide inhibitor of c-Jun N-terminal kinase protects against both aminoglycoside and acoustic trauma-induced auditory hair cell death and hearing loss.J Neurosci. 2003 Sep 17;23(24):8596-607. doi: 10.1523/JNEUROSCI.23-24-08596.2003. J Neurosci. 2003. PMID: 13679429 Free PMC article.
-
Blocking c-Jun-N-terminal kinase signaling can prevent hearing loss induced by both electrode insertion trauma and neomycin ototoxicity.Hear Res. 2007 Apr;226(1-2):168-77. doi: 10.1016/j.heares.2006.09.008. Epub 2006 Nov 13. Hear Res. 2007. PMID: 17098385
-
Prevention of cochlear implant electrode damage.Curr Opin Otolaryngol Head Neck Surg. 2006 Oct;14(5):323-8. doi: 10.1097/01.moo.0000244189.74431.df. Curr Opin Otolaryngol Head Neck Surg. 2006. PMID: 16974145 Review.
-
Mechanisms of hearing loss from trauma and inflammation: otoprotective therapies from the laboratory to the clinic.Acta Otolaryngol. 2010 Mar;130(3):308-11. doi: 10.1080/00016480903124655. Acta Otolaryngol. 2010. PMID: 19579145 Review.
Cited by
-
Extracellular Vesicles in Inner Ear Therapies-Pathophysiological, Manufacturing, and Clinical Considerations.J Clin Med. 2022 Dec 15;11(24):7455. doi: 10.3390/jcm11247455. J Clin Med. 2022. PMID: 36556073 Free PMC article. Review.
-
[Cochlear implants and tinnitus].HNO. 2015 Apr;63(4):291-7. doi: 10.1007/s00106-014-2975-5. HNO. 2015. PMID: 25862623 German.
-
Dual Release Carriers for Cochlear Delivery.Adv Healthc Mater. 2016 Jan 7;5(1):94-100. doi: 10.1002/adhm.201500141. Epub 2015 Jul 14. Adv Healthc Mater. 2016. PMID: 26178272 Free PMC article. No abstract available.
-
[Biological therapies in otology. German version].HNO. 2017 Jul;65(7):571-585. doi: 10.1007/s00106-016-0304-x. HNO. 2017. PMID: 28204850 German.
-
Influence of electrode array stiffness and diameter on hearing in cochlear implanted guinea pig.PLoS One. 2017 Aug 24;12(8):e0183674. doi: 10.1371/journal.pone.0183674. eCollection 2017. PLoS One. 2017. PMID: 28837630 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Research Materials
Miscellaneous