Literature DB >> 10985285

Physiological patterns in the hippocampo-entorhinal cortex system.

J J Chrobak1, A Lörincz, G Buzsáki.   

Abstract

The anatomical connectivity and intrinsic properties of entorhinal cortical neurons give rise to ordered patterns of ensemble activity. How entorhinal ensembles form, interact, and accomplish emergent processes such as memory formation is not well-understood. We lack sufficient understanding of how neuronal ensembles in general can function transiently and distinctively from other neuronal ensembles. Ensemble interactions are bound, foremost, by anatomical connectivity and temporal constraints on neuronal discharge. We present an overview of the structure of neuronal interactions within the entorhinal cortex and the rest of the hippocampal formation. We wish to highlight two principle features of entorhinal-hippocampal interactions. First, large numbers of entorhinal neurons are organized into at least two distinct high-frequency population patterns: gamma (40-100 Hz) frequency volleys and ripple (140-200 Hz) frequency volleys. These patterns occur coincident with other well-defined electrophysiological patterns. Gamma frequency volleys are modulated by the theta cycle. Ripple frequency volleys occur on each sharp wave event. Second, these patterns occur dominantly in specific layers of the entorhinal cortex. Theta/gamma frequency volleys are the principle pattern observed in layers I-III, in the neurons that receive cortical inputs and project to the hippocampus. Ripple frequency volleys are the principle population pattern observed in layers V-VI, in the neurons that receive hippocampal output and project primarily to the neocortex. Further, we will highlight how these ensemble patterns organize interactions within distributed forebrain structures and support memory formation.

Mesh:

Year:  2000        PMID: 10985285     DOI: 10.1002/1098-1063(2000)10:4<457::AID-HIPO12>3.0.CO;2-Z

Source DB:  PubMed          Journal:  Hippocampus        ISSN: 1050-9631            Impact factor:   3.899


  51 in total

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2.  Nonpharmacological amelioration of age-related learning deficits: the impact of hippocampal theta-triggered training.

Authors:  Yukiko Asaka; Kristin N Mauldin; Amy L Griffin; Matthew A Seager; Elizabeth Shurell; Stephen D Berry
Journal:  Proc Natl Acad Sci U S A       Date:  2005-09-06       Impact factor: 11.205

3.  Developmental emergence of hippocampal fast-field "ripple" oscillations in the behaving rat pups.

Authors:  D L Buhl; G Buzsáki
Journal:  Neuroscience       Date:  2005       Impact factor: 3.590

4.  Heterogeneous spatial patterns of long-term potentiation in rat hippocampal slices.

Authors:  Payne Y Chang; Meyer B Jackson
Journal:  J Physiol       Date:  2006-07-27       Impact factor: 5.182

5.  NMDA receptor-dependent switching between different gamma rhythm-generating microcircuits in entorhinal cortex.

Authors:  Steven Middleton; Jozsi Jalics; Tilman Kispersky; Fiona E N Lebeau; Anita K Roopun; Nancy J Kopell; Miles A Whittington; Mark O Cunningham
Journal:  Proc Natl Acad Sci U S A       Date:  2008-11-07       Impact factor: 11.205

6.  Parallel prefrontal pathways reach distinct excitatory and inhibitory systems in memory-related rhinal cortices.

Authors:  Jamie G Bunce; Basilis Zikopoulos; Marcia Feinberg; Helen Barbas
Journal:  J Comp Neurol       Date:  2013-12-15       Impact factor: 3.215

7.  Input-output features of anatomically identified CA3 neurons during hippocampal sharp wave/ripple oscillation in vitro.

Authors:  Norbert Hájos; Mária R Karlócai; Beáta Németh; István Ulbert; Hannah Monyer; Gábor Szabó; Ferenc Erdélyi; Tamás F Freund; Attila I Gulyás
Journal:  J Neurosci       Date:  2013-07-10       Impact factor: 6.167

8.  Shared rhythmic subcortical GABAergic input to the entorhinal cortex and presubiculum.

Authors:  Tim James Viney; Minas Salib; Abhilasha Joshi; Gunes Unal; Naomi Berry; Peter Somogyi
Journal:  Elife       Date:  2018-04-05       Impact factor: 8.140

9.  Dynamic cross-frequency couplings of local field potential oscillations in rat striatum and hippocampus during performance of a T-maze task.

Authors:  Adriano B L Tort; Mark A Kramer; Catherine Thorn; Daniel J Gibson; Yasuo Kubota; Ann M Graybiel; Nancy J Kopell
Journal:  Proc Natl Acad Sci U S A       Date:  2008-12-12       Impact factor: 11.205

10.  High frequency oscillations in intracranial EEGs mark epileptogenicity rather than lesion type.

Authors:  Julia Jacobs; Pierre Levan; Claude-Edouard Châtillon; André Olivier; François Dubeau; Jean Gotman
Journal:  Brain       Date:  2009-03-18       Impact factor: 13.501

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