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Persistent Na+ current modifies burst discharge by regulating conditional backpropagation of dendritic spikes
Brent Doiron1, Liza Noonan, Neal Lemon
1Department of Physics, University of Ottawa, Ontario K1N 6N5, Canada.
Journal of Neurophysiology
|January 11, 2003
Summary
Sensory neurons transition from tonic to burst firing using a depolarizing afterpotential (DAP) mechanism. This process, involving persistent sodium current (I(NaP)), regulates burst frequency for effective stimulus detection in electric fish.
Area of Science:
- Neuroscience
- Computational Neuroscience
- Electrophysiology
Background:
- Sensory neuron stimulus detection relies on firing mode transitions (tonic to burst).
- Pyramidal cells in electric fish electrosensory lobes use spike bursts for stimulus detection.
- Burst generation involves dendritic spike broadening, potentiating somatic depolarizing afterpotentials (DAPs).
Purpose of the Study:
- Investigate the mechanisms controlling the transition from tonic to burst firing in sensory neurons.
- Determine the factors regulating spike burst frequency in pyramidal cells.
- Explain the physiological basis for variable bursting dynamics.
Main Methods:
- In vitro electrophysiological recordings from weakly electric fish.
- Compartmental modeling of neuronal activity.
- Dynamical systems analysis to understand discharge thresholds.
Main Results:
- Burst frequency is regulated by the rate of DAP potentiation, influencing spike doublet discharge.
- Persistent sodium current (I(NaP)) magnifies DAP potentiation via positive feedback.
- A shift from tonic to burst discharge is induced by I(NaP)-mediated slow depolarization.
Conclusions:
- Conditional backpropagation, a rhythmic dendritic spike failure, converts tonic to burst discharge.
- The interaction between dendritic K+ current and I(NaP) explains variable bursting timescales.
- Neuronal firing mode transitions are explained by saddle-node bifurcations and underlying ionic mechanisms.