4.6 Article

Theta-gamma coupling emerges from spatially heterogeneous cholinergic neuromodulation

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PLOS COMPUTATIONAL BIOLOGY
卷 17, 期 7, 页码 -

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PUBLIC LIBRARY SCIENCE
DOI: 10.1371/journal.pcbi.1009235

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资金

  1. National Institute on Drug Abuse [R01DA045063]
  2. National Institute of Neurological Disorders and Stroke [PO50NS091856, R01 NS118440]
  3. National Institute of Mental Health [DP2 MH 104119]
  4. National Science Foundation [BCS-1749430]
  5. National Institute of Biomedical Imaging and Bioengineering [R01EB018297]

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Recent evidence suggests that spatially segregated acetylcholine (ACh) modulation can generate theta-modulated gamma rhythms in excitatory-inhibitory neural networks, providing novel insights into the mechanisms of ACh-regulated theta-gamma coupling. Stable gamma rhythms and theta-gamma coupling emerge in high-ACh regions, while theta or mixed theta-gamma activity occurs at the peripheries of these regions. This study highlights the causal role of spatially heterogenous ACh signaling in localized theta-gamma rhythmicity and its potential impact on attentional processing in the brain.
Author summary Recent evidence indicating that ACh signaling is both transient and spatially circumscribed raises the question of how this feature impacts information processing in cortical networks. Here we demonstrate that spatially segregated ACh modulation of excitatory-inhibitory neural networks generates theta-modulated gamma rhythms, a hallmark of attention and information processing. Theta-gamma coupling arises naturally as neuronal activity traverses high-ACh regions of the network, and gamma activity alternates between distinct high-ACh sites at theta frequency. These findings provide novel insights into neurophysiological mechanisms for ACh-regulated theta-gamma coupling and uncoupling. Theta and gamma rhythms and their cross-frequency coupling play critical roles in perception, attention, learning, and memory. Available data suggest that forebrain acetylcholine (ACh) signaling promotes theta-gamma coupling, although the mechanism has not been identified. Recent evidence suggests that cholinergic signaling is both temporally and spatially constrained, in contrast to the traditional notion of slow, spatially homogeneous, and diffuse neuromodulation. Here, we find that spatially constrained cholinergic stimulation can generate theta-modulated gamma rhythms. Using biophysically-based excitatory-inhibitory (E-I) neural network models, we simulate the effects of ACh on neural excitability by varying the conductance of a muscarinic receptor-regulated K+ current. In E-I networks with local excitatory connectivity and global inhibitory connectivity, we demonstrate that theta-gamma-coupled firing patterns emerge in ACh modulated network regions. Stable gamma-modulated firing arises within regions with high ACh signaling, while theta or mixed theta-gamma activity occurs at the peripheries of these regions. High gamma activity also alternates between different high-ACh regions, at theta frequency. Our results are the first to indicate a causal role for spatially heterogenous ACh signaling in the emergence of localized theta-gamma rhythmicity. Our findings also provide novel insights into mechanisms by which ACh signaling supports the brain region-specific attentional processing of sensory information.

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