PUBLICATION
Voltage dependence of the glycine receptor-channel kinetics in the zebrafish hindbrain
- Authors
- Legendre, P.
- ID
- ZDB-PUB-991216-2
- Date
- 1999
- Source
- Journal of neurophysiology 82(5): 2120-2129 (Journal)
- Registered Authors
- Legendre, Pascal
- Keywords
- none
- MeSH Terms
-
- Animals
- Evoked Potentials/drug effects
- Evoked Potentials/physiology*
- Excitatory Postsynaptic Potentials/drug effects
- Excitatory Postsynaptic Potentials/physiology
- Glycine/pharmacology*
- In Vitro Techniques
- Ion Channel Gating/physiology
- Ion Channels/drug effects
- Ion Channels/physiology*
- Kinetics
- Membrane Potentials
- Patch-Clamp Techniques
- Reaction Time
- Receptors, Glycine/physiology*
- Rhombencephalon/physiology*
- Zebrafish
- PubMed
- 10561392 Full text @ J. Neurophysiol.
Citation
Legendre, P. (1999) Voltage dependence of the glycine receptor-channel kinetics in the zebrafish hindbrain. Journal of neurophysiology. 82(5):2120-2129.
Abstract
Electrophysiological recordings of outside-out patches to fast-flow applications of glycine were made on patches derived from the Mauthner cells of the 50-h-old zebrafish larva. As for glycinergic miniature inhibitory postsynaptic currents (mIPSCs), depolarizing the patch produced a broadening of the transient outside-out current evoked by short applications (1 ms) of a saturating concentration of glycine (3 mM). When the outside-out patch was depolarized from -50 to +20 mV, the peak current varied linearly with voltage. A 1-ms application of 3 mM glycine evoked currents that activated rapidly and deactivated biexponentially with time constants of approximately 5 and approximately 30 ms (holding potential of -50 mV). These two decay time constants were increased by depolarization. The fast deactivation time constant increased e-fold per 95 mV. The relative amplitude of the two decay components did not significantly vary with voltage. The fast component represented 64.2 +/- 2.8% of the total current at -50 mV and 54.1 +/- 10% at +20 mV. The 20-80% rise time of these responses did not show any voltage dependence, suggesting that the opening rate constant is insensitive to voltage. The 20-80% rise time was 0.2 ms at -70 mV and 0.22 ms at +20 mV. Responses evoked by 100-200 ms application of a low concentration of glycine (0.1 mM) had a biphasic rising phase reflecting the complex gating behavior of the glycine receptor. The time constant of these two components and their relative amplitude did not change with voltage, suggesting that modal shifts in the glycine-activated channel gating mode are not sensitive to the membrane potential. Using a Markov model to simulate glycine receptor gating behavior, we were able to mimic the voltage-dependent change in the deactivation time course of the responses evoked by 1-ms application of 3 mM glycine. This kinetics model incorporates voltage-dependent closing rate constants. It provides a good description of the time course of the onset of responses evoked by the application of a low concentration of glycine at all membrane potentials tested.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping