Selective entrainment of gamma subbands by different slow network oscillations
Selective entrainment of gamma subbands by different slow network oscillations
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DOI:
10.1073/pnas.1617249114
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发表时间:
2017-04
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影响因子:
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通讯作者:
Weiwei Zhong;Mareva Ciatipis;Thérèse Wolfenstetter;Jakob Jessberger;C. Müller;S. Ponsel;Y. Yanovsky;J. Brankačk;A. Tort;A. Draguhn
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文献类型:
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作者:
Weiwei Zhong;Mareva Ciatipis;Thérèse Wolfenstetter;Jakob Jessberger;C. Müller;S. Ponsel;Y. Yanovsky;J. Brankačk;A. Tort;A. Draguhn
Significance Theta-gamma coupling has been largely documented in hippocampal and neocortical areas and hypothesized to constitute a network mechanism for information processing. However, we identify here another global slow rhythm at near-theta frequency that also couples to gamma. By simultaneously recording respiration, we could distinguish actual theta oscillations from a respiration-entrained rhythm (RR) in the local field potential whose peak frequency may overlap with theta. We demonstrate a robust specificity for the coupling of different gamma subbands to either theta or RR depending on brain state and region. The results suggest that the brain uses different frequency channels for transferring different types of information. Theta oscillations (4–12 Hz) are thought to provide a common temporal reference for the exchange of information among distant brain networks. On the other hand, faster gamma-frequency oscillations (30–160 Hz) nested within theta cycles are believed to underlie local information processing. Whether oscillatory coupling between global and local oscillations, as showcased by theta-gamma coupling, is a general coding mechanism remains unknown. Here, we investigated two different patterns of oscillatory network activity, theta and respiration-induced network rhythms, in four brain regions of freely moving mice: olfactory bulb (OB), prelimbic cortex (PLC), parietal cortex (PAC), and dorsal hippocampus [cornu ammonis 1 (CA1)]. We report differential state- and region-specific coupling between the slow large-scale rhythms and superimposed fast oscillations. During awake immobility, all four regions displayed a respiration-entrained rhythm (RR) with decreasing power from OB to CA1, which coupled exclusively to the 80- to 120-Hz gamma subband (γ2). During exploration, when theta activity was prevailing, OB and PLC still showed exclusive coupling of RR with γ2 and no theta-gamma coupling, whereas PAC and CA1 switched to selective coupling of theta with 40- to 80-Hz (γ1) and 120- to 160-Hz (γ3) gamma subbands. Our data illustrate a strong, specific interaction between neuronal activity patterns and respiration. Moreover, our results suggest that the coupling between slow and fast oscillations is a general brain mechanism not limited to the theta rhythm.