ArticleJournal of neurophysiology2013
Hippocampal CA1 pyramidal neurons exhibit type 1 phase-response curves and type 1 excitability.
Article in Journal of neurophysiology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.
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Who cites it
10 citing papers in PubMed.
- How neuronal morphology impacts the synchronisation state of neuronal networks.PLoS computational biology · 2024Article
- How to correctly quantify neuronal phase-response curves from noisy recordings.Journal of computational neuroscience · 2019Article
- Phase response theory explains cluster formation in sparsely but strongly connected inhibitory neural networks and effects of jitter due to sparse connectivity.Journal of neurophysiology · 2019Article
- Article
- Morphology controls how hippocampal CA1 pyramidal neuron responds to uniform electric fields: a biophysical modeling study.Scientific reports · 2017Article
- Phase-resetting as a tool of information transmission.Current opinion in neurobiology · 2015Review
- Critical slowing down governs the transition to neuron spiking.PLoS computational biology · 2015Article
- Optimal entrainment of heterogeneous noisy neurons.Frontiers in neuroscience · 2015Article
- Predicting the responses of repetitively firing neurons to current noise.PLoS computational biology · 2014Article
- Effect of heterogeneity and noise on cross frequency phase-phase and phase-amplitude coupling.Network (Bristol, England)Article
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4 authors.
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Abstract
Phase-resetting properties of neurons determine their functionality as integrators (type 1) vs. resonators (type 2), as well as their synchronization tendencies. We introduce a novel, bias-correction method to estimate the infinitesimal phase-resetting curve (iPRC) and confirm type 1 excitability in hippocampal pyramidal CA1 neurons in vitro by two independent methods. First, PRCs evoked using depolarizing pulses consisted only of advances, consistent with type 1. Second, the frequency/current (f/I) plots showed no minimum frequency, again consistent with type 1. Type 1 excitability was also confirmed by the absence of a resonant peak in the interspike interval histograms derived from the f/I data. The PRC bias correction assumed that the distribution of noisy phase resetting is truncated, because an input cannot advance a spike to a point in time before the input (the causal limit) and successfully removed the statistical bias for delays in the null PRC in response to zero-magnitude input by computing the phase resetting as the mean of the untruncated distribution. The PRC for depolarization peaked at late phases and decreased to zero by the end of the cycle, whereas delays observed in response to hyperpolarization increased monotonically. The bias correction did not affect this difference in shape, which was due instead to the causal limit obscuring the iPRC for depolarization but not hyperpolarization. Our results suggest that weak periodic hyperpolarizing drive can theoretically entrain CA1 pyramidal neurons at any phase but that strong excitation will preferentially phase-lock them with zero time lag.
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