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Activity‐dependent excitability changes in hippocampal CA3 cell Schaffer axons
Author(s) -
Soleng A. F.,
Baginskas A.,
Andersen P.,
Raastad M.
Publication year - 2004
Publication title -
the journal of physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.802
H-Index - 240
eISSN - 1469-7793
pISSN - 0022-3751
DOI - 10.1113/jphysiol.2004.071225
Subject(s) - neuroscience , hippocampal formation , axon , hyperpolarization (physics) , chemistry , electrophysiology , stimulation , stimulus (psychology) , soma , biophysics , biology , psychology , organic chemistry , nuclear magnetic resonance spectroscopy , psychotherapist
The membrane potential changes following action potentials in thin unmyelinated cortical axons with en passant boutons may be important for synaptic release and conduction abilities of such axons. In the lack of intra‐axonal recording techniques we have used extracellular excitability testing as an indirect measure of the after‐potentials. We recorded from individual CA3 soma in hippocampal slices and activated the axon with a range of stimulus intensities. When conditioning and test stimuli were given to the same site the excitability changes were partly masked by local effects of the stimulating electrode at intervals < 5 ms. Therefore, we elicited the conditioning action potential from one axonal branch and tested the excitability of another branch. We found that a single action potential reduced the axonal excitability for 15 ms followed by an increased excitability for ∼200 ms at 24°C. Using field recordings of axonal action potentials we show that raising the temperature to 34°C reduced the magnitude and duration of the initial depression. However, the duration of the increased excitability was very similar (time constant 135 ± 20 ms) at 24 and 34°C, and with 2.0 and 0.5 m m Ca 2+ in the bath. At stimulus rates > 1 Hz, a condition that activates a hyperpolarization‐activated current ( I h ) in these axons, the decay was faster than at lower stimulation rates. This effect was reduced by the I h blocker ZD7288. These data suggest that the decay time course of the action potential‐induced hyperexcitability is determined by the membrane time constant.