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Characterization of Voltage-Gated Ca2+ Conductances in Layer 5 Neocortical Pyramidal Neurons from Rats
Author(s) -
Mara Almog,
Alon Korngreen
Publication year - 2009
Publication title -
plos one
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.99
H-Index - 332
ISSN - 1932-6203
DOI - 10.1371/journal.pone.0004841
Subject(s) - voltage dependent calcium channel , patch clamp , biophysics , voltage gated ion channel , chemistry , membrane potential , somatosensory system , conductance , electrophysiology , neuroscience , t type calcium channel , calcium , ion channel , biology , physics , biochemistry , receptor , organic chemistry , condensed matter physics
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.

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