KV1 and KV3 Potassium Channels Identified at Presynaptic Terminals of the Corticostriatal Synapses in Rat
| Autor: | Ana V. Vega, David Meneses, Francisco M. Torres‐Cruz, Jaime Barral |
|---|---|
| Jazyk: | angličtina |
| Rok vydání: | 2016 |
| Předmět: |
Male
0301 basic medicine Article Subject Presynaptic Terminals Dendrotoxin Action Potentials Biology lcsh:RC321-571 Tityustoxin 03 medical and health sciences chemistry.chemical_compound 0302 clinical medicine Potassium Channel Blockers medicine Animals Protein Isoforms Rats Wistar lcsh:Neurosciences. Biological psychiatry. Neuropsychiatry Cerebral Cortex Tetraethylammonium Margatoxin Phrixotoxin Potassium channel blocker Corpus Striatum Potassium channel Rats 030104 developmental biology Shaw Potassium Channels Neurology chemistry Synapses Shaker Superfamily of Potassium Channels Heteropodatoxin Neurology (clinical) Neuroscience 030217 neurology & neurosurgery Research Article medicine.drug |
| Zdroj: | Neural Plasticity, Vol 2016 (2016) Neural Plasticity |
| ISSN: | 2090-5904 |
| DOI: | 10.1155/2016/8782518 |
| Popis: | In the last years it has been increasingly clear thatKV-channel activity modulates neurotransmitter release. The subcellular localization and composition of potassium channels are crucial to understanding its influence on neurotransmitter release. To investigate the role ofKVin corticostriatal synapses modulation, we combined extracellular recording of population-spike and pharmacological blockage with specific and nonspecific blockers to identify several families ofKVchannels. We induced paired-pulse facilitation (PPF) and studied the changes in paired-pulse ratio (PPR) before and after the addition of specificKVblockers to determine whether particularKVsubtypes were located pre- or postsynaptically. Initially, the presence ofKVchannels was tested by exposing brain slices to tetraethylammonium or 4-aminopyridine; in both cases we observed a decrease in PPR that was dose dependent. Further experiments with tityustoxin, margatoxin, hongotoxin, agitoxin, dendrotoxin, and BDS-I toxins all rendered a reduction in PPR. In contrast heteropodatoxin and phrixotoxin had no effect. Our results reveal that corticostriatal presynapticKVchannels have a complex stoichiometry, including heterologous combinationsKV1.1,KV1.2,KV1.3, andKV1.6 isoforms, as well asKV3.4, but notKV4 channels. The variety ofKVchannels offers a wide spectrum of possibilities to regulate neurotransmitter release, providing fine-tuning mechanisms to modulate synaptic strength. |
| Databáze: | OpenAIRE |
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