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Postsynaptic action potentials do not alter short-term potentiation in the dentate gyrus
1School of Kinesiology, Simon Fraser University, Burnaby, B.C., Canada. barryf@sfu.ca
Brain Research
|May 30, 1997
Summary
Dendritic spikes in neurons were investigated for their role in paired-pulse facilitation (PPF), a short-term plasticity. Results indicate that dendritic action potentials do not contribute to the postsynaptic component of PPF in the dentate gyrus.
Area of Science:
- Neuroscience
- Cellular Neuroscience
- Synaptic Plasticity
Background:
- Dendrites of neocortical neurons can generate active action potentials that propagate back from the soma.
- These dendritic spikes have been hypothesized to play a role in various forms of synaptic plasticity.
- Paired-pulse facilitation (PPF) is a well-characterized form of short-term synaptic plasticity.
Purpose of the Study:
- To investigate the contribution of dendritic spikes to paired-pulse facilitation (PPF) in the dentate gyrus of hippocampal slices.
- To determine if dendritic action potentials influence the postsynaptic component of PPF.
Main Methods:
- Paired orthodromic stimulation of the perforant path in hippocampal slices.
- Measurement of population spike (PS) amplitude and field excitatory postsynaptic potential (fEPSP) slope.
- Analysis of input-output (I-O) relationships between fEPSP slope and PS amplitude.
- Utilizing electric field effects to manipulate granule cell excitability without altering synaptic drive.
Main Results:
- Paired stimulation resulted in significant facilitation of PS amplitude (167%) and a smaller increase in fEPSP slope (108%).
- Input-output analysis suggested a postsynaptic contribution to PPF.
- However, altering granule cell excitability via electric fields, which modified the conditioning population spike, did not affect the test response.
Conclusions:
- Dendritic action potentials do not appear to contribute to the postsynaptic component of paired-pulse facilitation in the dentate gyrus.
- The observed facilitation is likely mediated by other mechanisms, potentially presynaptic.