Hippocampal CA1 pyramidal neurons exhibit type 1 phase-response curves and type 1 excitability

• Published in: Journal of neurophysiology 2013-06, Vol.109 (11), p.2757-2766
• Main Authors: Wang, Shuoguo, Musharoff, Maximilian M, Canavier, Carmen C, Gasparini, Sonia
• Format: Article
• Language: English
• Subjects: Action Potentials; Animals; CA1 Region, Hippocampal - cytology; CA1 Region, Hippocampal - physiology; Male; Pyramidal Cells - physiology; Rats; Rats, Sprague-Dawley
• ISSN: 0022-3077; 1522-1598
• DOI: 10.1152/jn.00721.2012

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.