Global slowing of network oscillations in mouse neocortex by diazepam

Benzodiazepines have a broad spectrum of clinical applications including sedation, anti-anxiety, and anticonvulsive therapy. At the cellular level, benzodiazepines are allosteric modulators of GABA(A) receptors; they increase the efficacy of inhibition in neuronal networks by prolonging the duration...

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Bibliographic Details
Main Authors: Scheffzük, Claudia (Author) , Draguhn, Andreas (Author) , Brankačk, Jurij (Author)
Format: Article (Journal)
Language:English
Published: 2013
In: Neuropharmacology
Year: 2013, Volume: 65, Pages: 123-133
ISSN:1873-7064
DOI:10.1016/j.neuropharm.2012.09.014
Online Access:Verlag, kostenfrei, Volltext: https://doi.org/10.1016/j.neuropharm.2012.09.014
Verlag, kostenfrei, Volltext: https://www.sciencedirect.com/science/article/pii/S0028390812004868
Verlag, Volltext: http://dx.doi.org/10.1016/j.neuropharm.2012.09.014
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Author Notes:Claudia Scheffzük, Valeriy I. Kukushka, Alexei L. Vyssotski, Andreas Draguhn, Adriano B.L. Tort, Jurij Brankačk
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Summary:Benzodiazepines have a broad spectrum of clinical applications including sedation, anti-anxiety, and anticonvulsive therapy. At the cellular level, benzodiazepines are allosteric modulators of GABA(A) receptors; they increase the efficacy of inhibition in neuronal networks by prolonging the duration of inhibitory postsynaptic potentials. This mechanism of action predicts that benzodiazepines reduce the frequency of inhibition-driven network oscillations, consistent with observations from human and animal EEG. However, most of existing data are restricted to frequency bands below ∼30 Hz. Recent data suggest that faster cortical network rhythms are critically involved in several behavioral and cognitive tasks. We therefore analyzed diazepam effects on a large range of cortical network oscillations in freely moving mice, including theta (4-12 Hz), gamma (40-100 Hz) and fast gamma (120-160 Hz) oscillations. We also investigated diazepam effects over the coupling between theta phase and the amplitude fast oscillations. We report that diazepam causes a global slowing of oscillatory activity in all frequency domains. Oscillation power was changed differently for each frequency domain, with characteristic differences between active wakefulness, slow-wave sleep and REM sleep. Cross-frequency coupling strength, in contrast, was mostly unaffected by diazepam. Such state- and frequency-dependent actions of benzodiazepines on cortical network oscillations may be relevant for their specific cognitive effects. They also underline the strong interaction between local network oscillations and global brain states.
Item Description:Online veröffentlicht: 9. Oktober 2012
Gesehen am 16.12.2024
Physical Description:Online Resource
ISSN:1873-7064
DOI:10.1016/j.neuropharm.2012.09.014