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Inhibition of A-type potassium current by the peptide toxin SNX-482.
- Source :
-
The Journal of neuroscience : the official journal of the Society for Neuroscience [J Neurosci] 2014 Jul 09; Vol. 34 (28), pp. 9182-9. - Publication Year :
- 2014
-
Abstract
- SNX-482, a peptide toxin isolated from tarantula venom, has become widely used as an inhibitor of Cav2.3 voltage-gated calcium channels. Unexpectedly, we found that SNX-482 dramatically reduced the A-type potassium current in acutely dissociated dopamine neurons from mouse substantia nigra pars compacta. The inhibition persisted when calcium was replaced by cobalt, showing that it was not secondary to a reduction of calcium influx. Currents from cloned Kv4.3 channels expressed in HEK-293 cells were inhibited by SNX-482 with an IC50 of <3 nM, revealing substantially greater potency than for SNX-482 inhibition of Cav2.3 channels (IC50 20-60 nM). At sub-saturating concentrations, SNX-482 produced a depolarizing shift in the voltage dependence of activation of Kv4.3 channels and slowed activation kinetics. Similar effects were seen on gating of cloned Kv4.2 channels, but the inhibition was less pronounced and required higher toxin concentrations. These results reveal SNX-482 as the most potent inhibitor of Kv4.3 channels yet identified. Because of the effects on both Kv4.3 and Kv4.2 channels, caution is needed when interpreting the effects of SNX-482 on cells and circuits where these channels are present.<br /> (Copyright © 2014 the authors 0270-6474/14/349182-08$15.00/0.)
- Subjects :
- Animals
Cells, Cultured
Dopaminergic Neurons physiology
Female
HEK293 Cells
Humans
Inhibitory Concentration 50
Ion Channel Gating physiology
Male
Membrane Potentials physiology
Mice
Patch-Clamp Techniques
Potassium metabolism
Shal Potassium Channels physiology
Dopaminergic Neurons drug effects
Ion Channel Gating drug effects
Membrane Potentials drug effects
Potassium Channel Blockers pharmacology
Shal Potassium Channels drug effects
Spider Venoms pharmacology
Subjects
Details
- Language :
- English
- ISSN :
- 1529-2401
- Volume :
- 34
- Issue :
- 28
- Database :
- MEDLINE
- Journal :
- The Journal of neuroscience : the official journal of the Society for Neuroscience
- Publication Type :
- Academic Journal
- Accession number :
- 25009251
- Full Text :
- https://doi.org/10.1523/JNEUROSCI.0339-14.2014