2000
DOI: 10.1038/79848
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Cellular and network mechanisms of rhythmic recurrent activity in neocortex

Abstract: The neocortex generates periods of recurrent activity, such as the slow (0.1-0.5 Hz) oscillation during slow-wave sleep. Here we demonstrate that slices of ferret neocortex maintained in vitro generate this slow (< 1 Hz) rhythm when placed in a bathing medium that mimics the extracellular ionic composition in situ. This slow oscillation seems to be initiated in layer 5 as an excitatory interaction between pyramidal neurons and propagates through the neocortex. Our results demonstrate that the cerebral cortex g… Show more

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Cited by 1,370 publications
(1,595 citation statements)
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“…Another non–mutually exclusive possibility is that the complexity of residual thalamocortical networks may be reduced by functional imbalances leading to an excessive degree of neuronal bistability 42. This may happen, for example, following changes in the neuromodulatory milieu, when potassium currents are abnormally increased and when the balance between excitation and inhibition is disrupted 43, 44. In this regard, it is worth recalling that low complexity responses to cortical stimulation are the rule during states such as anesthesia18 and NREM sleep,45 when bistability is present but can be readily reversed 46…”
Section: Discussionmentioning
confidence: 99%
“…Another non–mutually exclusive possibility is that the complexity of residual thalamocortical networks may be reduced by functional imbalances leading to an excessive degree of neuronal bistability 42. This may happen, for example, following changes in the neuromodulatory milieu, when potassium currents are abnormally increased and when the balance between excitation and inhibition is disrupted 43, 44. In this regard, it is worth recalling that low complexity responses to cortical stimulation are the rule during states such as anesthesia18 and NREM sleep,45 when bistability is present but can be readily reversed 46…”
Section: Discussionmentioning
confidence: 99%
“…In the cortex, this hallmark of spontaneous activity has been reported since the earliest culture success in vitro (Crain, 1966;Calvet, 1974) and naturally occurs in all isolated cortex preparations thus studied, e.g. in organotypic cultures (Plenz and Aertsen, 1996a;Plenz and Aertsen, 1996b;Gorba, Klostermann et al, 1999;Klostermann and Wahle, 1999;Baker, Corner et al, 2006), dissociated cultures (Maeda, Robinson et al, 1995;Gopal and Gross, 1996;Kamioka, Maeda et al, 1996;Canepari, Bove et al, 1997;Jimbo, Kawana et al, 2000;Segev, Shapira et al, 2001;van Pelt, Corner et al, 2004;Eytan and Marom, 2006), acute cortex slices (Sanchez-Vives and McCormick, 2000), and acutely isolated cortical slabs in vivo (Steriade, Nuñez et al, 1993;Timofeev, Grenier et al, 2000). Quantification of these Correspondence: Dr. Dietmar Plenz, Section on Critical Brain Dynamics, National Institute of Mental Health, Porter Neuroscience Research Center, Bldg.…”
Section: Introductionmentioning
confidence: 99%
“…Isolating the cortical tissue in vivo by creating cortical ''slabs'' first lead to a silent network, but activity recurs after a few days (Burns and Webb, 1979;Timofeev et al, 2000). In vitro cortical networks can also display self-sustained activity, as found in cortical slices (Sanchez-Vives and McCormick, 2000;Cossart et al, 2003) or in organotypic cultures of cortical neurons (Plenz and Aertsen, 1996).…”
Section: Introductionmentioning
confidence: 99%