A role for fast rhythmic bursting neurons in cortical gamma oscillations in vitro.

Mark O Cunningham, Miles A Whittington, Andrea Bibbig, Anita Roopun, Fiona E N LeBeau, Angelika Vogt, Hannah Monyer, Eberhard H Buhl, Roger D Traub
Author Information
  1. Mark O Cunningham: School of Biomedical Sciences, The Worsley Building, University of Leeds, Leeds LS2 9JT, United Kingdom.

Abstract

Basic cellular and network mechanisms underlying gamma frequency oscillations (30-80 Hz) have been well characterized in the hippocampus and associated structures. In these regions, gamma rhythms are seen as an emergent property of networks of principal cells and fast-spiking interneurons. In contrast, in the neocortex a number of elegant studies have shown that specific types of principal neuron exist that are capable of generating powerful gamma frequency outputs on the basis of their intrinsic conductances alone. These fast rhythmic bursting (FRB) neurons (sometimes referred to as "chattering" cells) are activated by sensory stimuli and generate multiple action potentials per gamma period. Here, we demonstrate that FRB neurons may function by providing a large-scale input to an axon plexus consisting of gap-junctionally connected axons from both FRB neurons and their anatomically similar counterparts regular spiking neurons. The resulting network gamma oscillation shares all of the properties of gamma oscillations generated in the hippocampus but with the additional critical dependence on multiple spiking in FRB cells.

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MeSH Term

Animals
Anticonvulsants
Auditory Cortex
Electroencephalography
Hippocampus
Male
Neural Conduction
Neurons
Phenytoin
Rats

Chemicals

Anticonvulsants
Phenytoin

Word Cloud

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