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Promoting neurite outgrowth from spiral ganglion neuron explants using polypyrrole/BDNF-coated electrodes
Journal of biomedical materials research. Part A, 2009-10, Vol.91A (1), p.241-250
Evans, Alison J.
Thompson, Brianna C.
Wallace, Gordon G.
Millard, Rodney
O'Leary, Stephen J.
Clark, Graeme M.
Shepherd, Robert K.
Richardson, Rachael T.
2009
Volltextzugriff (PDF)
Details
Autor(en) / Beteiligte
Evans, Alison J.
Thompson, Brianna C.
Wallace, Gordon G.
Millard, Rodney
O'Leary, Stephen J.
Clark, Graeme M.
Shepherd, Robert K.
Richardson, Rachael T.
Titel
Promoting neurite outgrowth from spiral ganglion neuron explants using polypyrrole/BDNF-coated electrodes
Ist Teil von
Journal of biomedical materials research. Part A, 2009-10, Vol.91A (1), p.241-250
Ort / Verlag
Hoboken: Wiley Subscription Services, Inc., A Wiley Company
Erscheinungsjahr
2009
Quelle
MEDLINE
Beschreibungen/Notizen
Release of neurotrophin‐3 (NT3) and brain‐derived neurotrophic factor (BDNF) from hair cells in the cochlea is essential for the survival of spiral ganglion neurons (SGNs). Loss of hair cells associated with a sensorineural hearing loss therefore results in degeneration of SGNs, potentially reducing the performance of a cochlear implant. Exogenous replacement of either or both neurotrophins protects SGNs from degeneration after deafness. We previously incorporated NT3 into the conducting polymer polypyrrole (Ppy) synthesized with para‐toluene sulfonate (pTS) to investigate whether Ppy/pTS/NT3‐coated cochlear implant electrodes could provide both neurotrophic support and electrical stimulation for SGNs. Enhanced and controlled release of NT3 was achieved when Ppy/pTS/NT3‐coated electrodes were subjected to electrical stimulation. Here we describe the release dynamics and biological properties of Ppy/pTS with incorporated BDNF. Release studies demonstrated slow passive diffusion of BDNF from Ppy/pTS/BDNF, with electrical stimulation significantly enhancing BDNF release over 7 days. A 3‐day SGN explant assay found that neurite outgrowth from explants was 12.3‐fold greater when polymers contained BDNF (p < 0.001), although electrical stimulation did not increase neurite outgrowth further. The versatility of Ppy to store and release neurotrophins, conduct electrical charge, and act as a substrate for nerve‐electrode interactions is discussed for specialized applications such as cochlear implants. © 2008 Wiley Periodicals, Inc. J Biomed Mater Res, 2009
Sprache
Englisch
Identifikatoren
ISSN: 1549-3296, 1552-4965
eISSN: 1552-4965
DOI: 10.1002/jbm.a.32228
Titel-ID: cdi_proquest_miscellaneous_869583572
Format
–
Schlagworte
Animals
,
Benzenesulfonates - chemistry
,
brain-derived neurotrophic factor
,
Brain-Derived Neurotrophic Factor - administration & dosage
,
Cells, Cultured
,
cochlear implant
,
Cochlear Implants
,
Diffusion
,
Electric Stimulation
,
electrical stimulation
,
Electrodes
,
Equipment Design
,
Ganglia - cytology
,
Neurites - metabolism
,
Neurons - cytology
,
Polymers - chemistry
,
polypyrrole
,
Pyrroles - chemistry
,
Rats
,
Rats, Wistar
,
sensorineural hearing loss
,
Spiral Ganglion
,
spiral ganglion neuron
,
Tissue Engineering - instrumentation
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