Upper stimulation threshold for retinal ganglion cell activation.
Details
Serval ID
serval:BIB_129028A80BDB
Type
Article: article from journal or magazin.
Collection
Publications
Institution
Title
Upper stimulation threshold for retinal ganglion cell activation.
Journal
Journal of neural engineering
ISSN
1741-2552 (Electronic)
ISSN-L
1741-2552
Publication state
Published
Issued date
08/2018
Peer-reviewed
Oui
Volume
15
Number
4
Pages
046012
Language
english
Notes
Publication types: Journal Article ; Research Support, Non-U.S. Gov't
Publication Status: ppublish
Publication Status: ppublish
Abstract
The existence of an upper threshold in electrically stimulated retinal ganglion cells (RGCs) is of interest because of its relevance to the development of visual prosthetic devices, which are designed to restore partial sight to blind patients. The upper threshold is defined as the stimulation level above which no action potentials (direct spikes) can be elicited in electrically stimulated retina.
We collected and analyzed in vitro recordings from rat RGCs in response to extracellular biphasic (anodic-cathodic) pulse stimulation of varying amplitudes and pulse durations. Such responses were also simulated using a multicompartment model.
We identified the individual cell variability in response to stimulation and the phenomenon known as upper threshold in all but one of the recorded cells (n = 20/21). We found that the latencies of spike responses relative to stimulus amplitude had a characteristic U-shape. In silico, we showed that the upper threshold phenomenon was observed only in the soma. For all tested biphasic pulse durations, electrode positions, and pulse amplitudes above lower threshold, a propagating action potential was observed in the distal axon. For amplitudes above the somatic upper threshold, the axonal action potential back-propagated in the direction of the soma, but the soma's low level of hyperpolarization prevented action potential generation in the soma itself.
An upper threshold observed in the soma does not prevent spike conductance in the axon.
We collected and analyzed in vitro recordings from rat RGCs in response to extracellular biphasic (anodic-cathodic) pulse stimulation of varying amplitudes and pulse durations. Such responses were also simulated using a multicompartment model.
We identified the individual cell variability in response to stimulation and the phenomenon known as upper threshold in all but one of the recorded cells (n = 20/21). We found that the latencies of spike responses relative to stimulus amplitude had a characteristic U-shape. In silico, we showed that the upper threshold phenomenon was observed only in the soma. For all tested biphasic pulse durations, electrode positions, and pulse amplitudes above lower threshold, a propagating action potential was observed in the distal axon. For amplitudes above the somatic upper threshold, the axonal action potential back-propagated in the direction of the soma, but the soma's low level of hyperpolarization prevented action potential generation in the soma itself.
An upper threshold observed in the soma does not prevent spike conductance in the axon.
Keywords
Action Potentials/physiology, Animals, Electric Stimulation/methods, Female, Photic Stimulation/methods, Rats, Rats, Long-Evans, Retinal Ganglion Cells/physiology
Pubmed
Web of science
Open Access
Yes
Create date
21/03/2024 11:48
Last modification date
22/03/2024 8:25