Characterization of voltage-gated Ca(2+) conductances in layer 5 neocortical pyramidal neurons from rats.

Neuronal voltage-gated Ca(2+) channels are involved in electrical signalling and in converting these signals into cytoplasmic calcium changes. One important function of voltage-gated Ca(2+) channels is generating regenerative dendritic Ca(2+) spikes. However, the Ca(2+) dependent mechanisms used to...

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Main Authors: Mara Almog, Alon Korngreen
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2009-01-01
Series:PLoS ONE
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/19337371/pdf/?tool=EBI
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spelling doaj-04ed304544e74087b361e407c220aa912021-03-03T22:40:50ZengPublic Library of Science (PLoS)PLoS ONE1932-62032009-01-0144e484110.1371/journal.pone.0004841Characterization of voltage-gated Ca(2+) conductances in layer 5 neocortical pyramidal neurons from rats.Mara AlmogAlon KorngreenNeuronal voltage-gated Ca(2+) channels are involved in electrical signalling and in converting these signals into cytoplasmic calcium changes. One important function of voltage-gated Ca(2+) channels is generating regenerative dendritic Ca(2+) spikes. However, the Ca(2+) dependent mechanisms used to create these spikes are only partially understood. To start investigating this mechanism, we set out to kinetically and pharmacologically identify the sub-types of somatic voltage-gated Ca(2+) channels in pyramidal neurons from layer 5 of rat somatosensory cortex, using the nucleated configuration of the patch-clamp technique. The activation kinetics of the total Ba(2+) current revealed conductance activation only at medium and high voltages suggesting that T-type calcium channels were not present in the patches. Steady-state inactivation protocols in combination with pharmacology revealed the expression of R-type channels. Furthermore, pharmacological experiments identified 5 voltage-gated Ca(2+) channel sub-types - L-, N-, R- and P/Q-type. Finally, the activation of the Ca(2+) conductances was examined using physiologically derived voltage-clamp protocols including a calcium spike protocol and a mock back-propagating action potential (mBPAP) protocol. These experiments enable us to suggest the possible contribution of the five Ca(2+) channel sub-types to Ca(2+) current flow during activation under physiological conditions.https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/19337371/pdf/?tool=EBI
collection DOAJ
language English
format Article
sources DOAJ
author Mara Almog
Alon Korngreen
spellingShingle Mara Almog
Alon Korngreen
Characterization of voltage-gated Ca(2+) conductances in layer 5 neocortical pyramidal neurons from rats.
PLoS ONE
author_facet Mara Almog
Alon Korngreen
author_sort Mara Almog
title Characterization of voltage-gated Ca(2+) conductances in layer 5 neocortical pyramidal neurons from rats.
title_short Characterization of voltage-gated Ca(2+) conductances in layer 5 neocortical pyramidal neurons from rats.
title_full Characterization of voltage-gated Ca(2+) conductances in layer 5 neocortical pyramidal neurons from rats.
title_fullStr Characterization of voltage-gated Ca(2+) conductances in layer 5 neocortical pyramidal neurons from rats.
title_full_unstemmed Characterization of voltage-gated Ca(2+) conductances in layer 5 neocortical pyramidal neurons from rats.
title_sort characterization of voltage-gated ca(2+) conductances in layer 5 neocortical pyramidal neurons from rats.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2009-01-01
description Neuronal voltage-gated Ca(2+) channels are involved in electrical signalling and in converting these signals into cytoplasmic calcium changes. One important function of voltage-gated Ca(2+) channels is generating regenerative dendritic Ca(2+) spikes. However, the Ca(2+) dependent mechanisms used to create these spikes are only partially understood. To start investigating this mechanism, we set out to kinetically and pharmacologically identify the sub-types of somatic voltage-gated Ca(2+) channels in pyramidal neurons from layer 5 of rat somatosensory cortex, using the nucleated configuration of the patch-clamp technique. The activation kinetics of the total Ba(2+) current revealed conductance activation only at medium and high voltages suggesting that T-type calcium channels were not present in the patches. Steady-state inactivation protocols in combination with pharmacology revealed the expression of R-type channels. Furthermore, pharmacological experiments identified 5 voltage-gated Ca(2+) channel sub-types - L-, N-, R- and P/Q-type. Finally, the activation of the Ca(2+) conductances was examined using physiologically derived voltage-clamp protocols including a calcium spike protocol and a mock back-propagating action potential (mBPAP) protocol. These experiments enable us to suggest the possible contribution of the five Ca(2+) channel sub-types to Ca(2+) current flow during activation under physiological conditions.
url https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/19337371/pdf/?tool=EBI
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