- Poster presentation
- Open Access
Distinct and competing interneuron populations can generate fast and slow gamma in oscillatory models of CA1
BMC Neuroscience volume 16, Article number: P119 (2015)
Gamma oscillations are widely observed in the mammalian brain and are important markers for cognition and attention [1, 2]. In CA1 of the hippocampus of freely moving rats, power in one of two distinct oscillatory bands in the gamma regime (fast gamma and slow gamma) is predominantly present at a given moment of time . Here, we demonstrate that models of networks with competing interneuron populations with different post-synaptic effects can create distinct oscillatory regimes that mimic the observed oscillations of CA1. Our network formulation reflects the following facts: 1) The duration of post-synaptic effect of an interneuron strongly influences the frequency in biophysical models of gamma oscillations . 2) The primary CA1 inputs from CA3 and the entorhinal cortex (EC) preferentially innervate interneurons of different subtype with different post-synaptic durations [5, 6].
We show that a firing rate model with competing interneuron populations with different post-synaptic time-constants is sufficient to generate slow and fast gamma oscillations. We conclude that mutual inhibition between the modeled interneuron populations permits switching in a bistable regime between distinct fast and slow gamma states. We also find similar behavior in spike-based network models. Our models explicitly predict the following about CA1: 1) Different interneurons innervated by different upstream regions phase-lock to different gamma states. 2) One population of interneurons is silenced, and another is active during fast and slow gamma events. 3) Mutual inhibition between interneuron populations is necessary for spontaneous switching of gamma state. Using experimental electrophysiological data from awake behaving rodents, we find interneurons that satisfy conditions 1 and 2, and we show putative 'fast' and 'slow' gamma interneurons categorized by their tendency to fire and phase-lock with oscillatory events as measured by a nearby local field potential.
Our 3-population firing rate model is schematized in Figure 1A. The dynamic variables are synaptic currents of an excitatory, fast inhibitory (IF) and slow inhibitory (Is) population; the firing rates are instantaneous functions of total input current. Fast excitation that interacts with inhibitory subpopulations supports oscillations. This interaction engages either one or both inhibitory subpopulations depending on IS - IF connectivity and input balance (Example in Figure 1B). This network oscillates at biophysically realistic frequencies given biophysically realistic network parameters. The fast inhibitory population, IF and slow inhibitory population, IS have post-synaptic time-constants of 5ms and 15ms, respectively. These roughly capture the diversity of post-synaptic inhibitory current time-courses of interneurons of different subtypes measured in CA1 . Our firing rate model demonstrates that with sufficient mutual inhibition between inhibitory populations, the oscillating network bifurcates into two stable regimes that oscillate at roughly the same frequencies as the observed fast and slow gamma oscillations [3, 7].
Previous experimental work suggests these two gamma oscillations reflect different information processing modes in the learning and memory system . Our models provide a mechanistic understanding of these modes and posit a new oscillatory role for distinct interneurons in CA1. Moreover, our models describe general oscillatory behavior in networks with distinct interneuron populations.
Fries P, Reynolds JH, Rorie AE, Desimone R: Modulation of oscillatory neuronal synchronization by selective visual attention. Science. 2001, 291 (5508): 1560-3.
Başar E, Başar-eroglu C, Karakaş S, Schürmann M: Gamma, alpha, delta, and theta oscillations govern cognitive processes. Int J Psychophysiol. 2001, 39 (2-3): 241-8.
Belluscio MA, Mizuseki K, Schmidt R, Kempter R, Buzsáki G: Cross-frequency phase-phase coupling between θ and γ oscillations in the hippocampus. J Neurosci. 2012, 32 (2): 423-35.
Jefferys JG, Traub RD, Whittington MA: Neuronal networks for induced '40 Hz' rhythms. Trends Neurosci. 1996, 19 (5): 202-8.
Gulyás AI, Megías M, Emri Z, Freund TF: Total number and ratio of excitatory and inhibitory synapses converging onto single interneurons of different types in the CA1 area of the rat hippocampus. J Neurosci. 1999, 19 (22): 10082-97.
Maccaferri G, Roberts JD, Szucs P, Cottingham CA, Somogyi P: Cell surface domain specific postsynaptic currents evoked by identified GABAergic neurones in rat hippocampus in vitro. J Physiol (Lond). 2000, 524 (Pt 1): 91-116.
Colgin LL, Denninger T, Fyhn M, Hafting T, Bonnevie T, Jensen O, Moser MB, Moser EI: Frequency of gamma oscillations routes flow of information in the hippocampus. Nature. 2009, 462 (7271): 353-7.
About this article
Cite this article
Keeley, S.L., Fenton, A.A. & Rinzel, J. Distinct and competing interneuron populations can generate fast and slow gamma in oscillatory models of CA1. BMC Neurosci 16, P119 (2015). https://doi.org/10.1186/1471-2202-16-S1-P119
- Local Field Potential
- Gamma Oscillation
- Mutual Inhibition
- Inhibitory Population
- Bistable Regime