Abstract
The synchronization of cortical gamma oscillatory activity (25β80 Hz) is thought to coordinate neuronal assemblies in the processing and storage of information. The mechanism by which independently oscillating and distantly located cortical zones become synchronized is presumed to involve activity in corticocortical connections, although evidence supporting this conjecture has only been indirect. In the present study, we show that activation of synaptic inputs within and to the medial entorhinal cortex (mEC) of the in vitro isolated guinea pig brain preparation resets the phase of ongoing gamma activity induced by muscarinic receptor agonism with carbachol (frequency: 24 Β± 2 Hz at 32Β°C). Phase reset was associated with a transient enhancement of the synchronization of gamma activity recorded at distant (>1 mm) mEC sites, across which low coherence (>0.75) was observed before stimulation. This increase in synchronization, as measured by crossβcorrelation analysis, was restricted to a maximal period of 200 ms after either local mEC or CA1 afferent stimulation. The results provide direct evidence that synaptic activation can enhance the rhythmic synchronization of spatially remote, independently oscillating neuronal assemblies in the mEC through a mechanism of synaptically evoked phase reset. Dynamic functional grouping of oscillatory discharges across long distances in the mEC may underlie coding processes involved in the integration and storage of incoming information and thus may be important for the role of this region in memory processes. Hippocampus 2002;12:447β456. Β© 2002 WileyβLiss, Inc.