Phosphodiesterase type 4 inhibitor rolipram improves survival of spiral ganglion neurons in vitro.

Sensorineural deafness is caused by damage of hair cells followed by degeneration of the spiral ganglion neurons and can be moderated by cochlear implants. However, the benefit of the cochlear implant depends on the excitability of the spiral ganglion neurons. Therefore, current research focuses on...

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Main Authors: Katharina Kranz, Athanasia Warnecke, Thomas Lenarz, Martin Durisin, Verena Scheper
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2014-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3958480?pdf=render
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spelling doaj-72df44c2231d41328a149ec6e80a52722020-11-25T01:19:08ZengPublic Library of Science (PLoS)PLoS ONE1932-62032014-01-0193e9215710.1371/journal.pone.0092157Phosphodiesterase type 4 inhibitor rolipram improves survival of spiral ganglion neurons in vitro.Katharina KranzAthanasia WarneckeThomas LenarzMartin DurisinVerena ScheperSensorineural deafness is caused by damage of hair cells followed by degeneration of the spiral ganglion neurons and can be moderated by cochlear implants. However, the benefit of the cochlear implant depends on the excitability of the spiral ganglion neurons. Therefore, current research focuses on the identification of agents that will preserve their degeneration. In this project we investigated the neuroprotective effect of Rolipram as a promising agent to improve the viability of the auditory neurons. It is a pharmaceutical agent that acts by selective inhibition of the phosphodiesterase 4 leading to an increase in cyclic AMP. Different studies reported a neuroprotective effect of Rolipram. However, its significance for the survival of SGN has not been reported so far. Thus, we isolated spiral ganglion cells of neonatal rats for cultivation with different Rolipram concentrations and determined the neuronal survival rate. Furthermore, we examined immunocytologically distinct proteins that might be involved in the neuroprotective signalling pathway of Rolipram and determined endogenous BDNF by ELISA. When applied at a concentration of 0.1 nM, Rolipram improved the survival of SGN in vitro. According to previous studies, our immunocytological data showed that Rolipram application induces the phosphorylation and thereby activation of the transcription factor CREB. This activation can be mediated by the cAMP-PKA-signalling pathway as well as via ERK as a part of the MAP-kinase pathway. However, only in cultures pre-treated with BDNF, an endogenous increase of BDNF was detected. We conclude that Rolipram has the potential to improve the vitality of neonatal auditory nerve cells in vitro. Further investigations are necessary to prove the effect of Rolipram in vivo in the adult organism after lesion of the hair cells and insertion of cochlear implants.http://europepmc.org/articles/PMC3958480?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Katharina Kranz
Athanasia Warnecke
Thomas Lenarz
Martin Durisin
Verena Scheper
spellingShingle Katharina Kranz
Athanasia Warnecke
Thomas Lenarz
Martin Durisin
Verena Scheper
Phosphodiesterase type 4 inhibitor rolipram improves survival of spiral ganglion neurons in vitro.
PLoS ONE
author_facet Katharina Kranz
Athanasia Warnecke
Thomas Lenarz
Martin Durisin
Verena Scheper
author_sort Katharina Kranz
title Phosphodiesterase type 4 inhibitor rolipram improves survival of spiral ganglion neurons in vitro.
title_short Phosphodiesterase type 4 inhibitor rolipram improves survival of spiral ganglion neurons in vitro.
title_full Phosphodiesterase type 4 inhibitor rolipram improves survival of spiral ganglion neurons in vitro.
title_fullStr Phosphodiesterase type 4 inhibitor rolipram improves survival of spiral ganglion neurons in vitro.
title_full_unstemmed Phosphodiesterase type 4 inhibitor rolipram improves survival of spiral ganglion neurons in vitro.
title_sort phosphodiesterase type 4 inhibitor rolipram improves survival of spiral ganglion neurons in vitro.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2014-01-01
description Sensorineural deafness is caused by damage of hair cells followed by degeneration of the spiral ganglion neurons and can be moderated by cochlear implants. However, the benefit of the cochlear implant depends on the excitability of the spiral ganglion neurons. Therefore, current research focuses on the identification of agents that will preserve their degeneration. In this project we investigated the neuroprotective effect of Rolipram as a promising agent to improve the viability of the auditory neurons. It is a pharmaceutical agent that acts by selective inhibition of the phosphodiesterase 4 leading to an increase in cyclic AMP. Different studies reported a neuroprotective effect of Rolipram. However, its significance for the survival of SGN has not been reported so far. Thus, we isolated spiral ganglion cells of neonatal rats for cultivation with different Rolipram concentrations and determined the neuronal survival rate. Furthermore, we examined immunocytologically distinct proteins that might be involved in the neuroprotective signalling pathway of Rolipram and determined endogenous BDNF by ELISA. When applied at a concentration of 0.1 nM, Rolipram improved the survival of SGN in vitro. According to previous studies, our immunocytological data showed that Rolipram application induces the phosphorylation and thereby activation of the transcription factor CREB. This activation can be mediated by the cAMP-PKA-signalling pathway as well as via ERK as a part of the MAP-kinase pathway. However, only in cultures pre-treated with BDNF, an endogenous increase of BDNF was detected. We conclude that Rolipram has the potential to improve the vitality of neonatal auditory nerve cells in vitro. Further investigations are necessary to prove the effect of Rolipram in vivo in the adult organism after lesion of the hair cells and insertion of cochlear implants.
url http://europepmc.org/articles/PMC3958480?pdf=render
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