scholarly journals Anatomical and physiological foundations of cerebello-hippocampal interactions

2018 ◽  
Author(s):  
TC Watson ◽  
P Obiang ◽  
A Torres-Herraez ◽  
A Wattilliaux ◽  
P Coulon ◽  
...  
Keyword(s):  
Neural Network ◽  
Motor Control ◽  
Local Field ◽  
Dorsal Hippocampus ◽  
Spatial Navigation ◽  
Field Potential ◽  
Spatial Processing ◽  
Frequency Range ◽  
Neuronal Oscillations ◽  
Lines Of Evidence

AbstractMultiple lines of evidence suggest that functionally intact cerebello-hippocampal interactions are required for appropriate spatial processing. However, how the cerebellum anatomically and physiologically engages with the hippocampus to sustain such interactions remains unknown. Using rabies virus as retrograde transneuronal tracer, we reveal that the dorsal hippocampus receives input from topographically restricted and disparate regions of the cerebellum. By simultaneously recording local field potential from both the dorsal hippocampus and anatomically connected cerebellar regions, we additionally demonstrate that the two structures interact, in a behaviorally dynamic manner, through subregion-specific synchronization of neuronal oscillations in the 6-12Hz frequency range. Together, these results reveal a novel neural network macro-architecture through which we can understand how a brain region classically associated with motor control, the cerebellum, may influence hippocampal neuronal activity and related functions, such as spatial navigation.

scholarly journals Anatomical and physiological foundations of cerebello-hippocampal interaction

eLife ◽  
2019 ◽  
Vol 8 ◽  
Author(s):  
Thomas Charles Watson ◽  
Pauline Obiang ◽  
Arturo Torres-Herraez ◽  
Aurélie Watilliaux ◽  
Patrice Coulon ◽  
...  
Keyword(s):  
Neural Network ◽  
Motor Control ◽  
Local Field ◽  
Dorsal Hippocampus ◽  
Spatial Navigation ◽  
Field Potential ◽  
Spatial Processing ◽  
Frequency Range ◽  
Neuronal Oscillations ◽  
Lines Of Evidence

Multiple lines of evidence suggest that functionally intact cerebello-hippocampal interactions are required for appropriate spatial processing. However, how the cerebellum anatomically and physiologically engages with the hippocampus to sustain such communication remains unknown. Using rabies virus as a retrograde transneuronal tracer in mice, we reveal that the dorsal hippocampus receives input from topographically restricted and disparate regions of the cerebellum. By simultaneously recording local field potential from both the dorsal hippocampus and anatomically connected cerebellar regions, we additionally suggest that the two structures interact, in a behaviorally dynamic manner, through subregion-specific synchronization of neuronal oscillations in the 6–12 Hz frequency range. Together, these results reveal a novel neural network macro-architecture through which we can understand how a brain region classically associated with motor control, the cerebellum, may influence hippocampal neuronal activity and related functions, such as spatial navigation.

Vagus Nerve Stimulation Induced Synchrony Modulation of Local Field Potential in the Rat Cerebral Cortex

2013 ◽  
Vol 133 (8) ◽  
pp. 1493-1500 ◽  
Author(s):  
Ryuji Kano ◽  
Kenichi Usami ◽  
Takahiro Noda ◽  
Tomoyo I. Shiramatsu ◽  
Ryohei Kanzaki ◽  
...  
Keyword(s):  
Cerebral Cortex ◽  
Vagus Nerve ◽  
Local Field ◽  
Nerve Stimulation ◽  
Local Field Potential ◽  
Vagus Nerve Stimulation ◽  
Field Potential ◽  
Rat Cerebral Cortex

scholarly journals Sensory feedback-dependent coding of arm position in local field potentials of the posterior parietal cortex

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Paul VanGilder ◽  
Ying Shi ◽  
Gregory Apker ◽  
Christopher A. Buneo
Keyword(s):  
Local Field ◽  
Sensory Feedback ◽  
Posterior Parietal Cortex ◽  
Spectral Power ◽  
Field Potential ◽  
Beta Activity ◽  
Beta Band ◽  
Arm Position ◽  
Multisensory Interactions ◽  
Spiking Activity

AbstractAlthough multisensory integration is crucial for sensorimotor function, it is unclear how visual and proprioceptive sensory cues are combined in the brain during motor behaviors. Here we characterized the effects of multisensory interactions on local field potential (LFP) activity obtained from the superior parietal lobule (SPL) as non-human primates performed a reaching task with either unimodal (proprioceptive) or bimodal (visual-proprioceptive) sensory feedback. Based on previous analyses of spiking activity, we hypothesized that evoked LFP responses would be tuned to arm location but would be suppressed on bimodal trials, relative to unimodal trials. We also expected to see a substantial number of recording sites with enhanced beta band spectral power for only one set of feedback conditions (e.g. unimodal or bimodal), as was previously observed for spiking activity. We found that evoked activity and beta band power were tuned to arm location at many individual sites, though this tuning often differed between unimodal and bimodal trials. Across the population, both evoked and beta activity were consistent with feedback-dependent tuning to arm location, while beta band activity also showed evidence of response suppression on bimodal trials. The results suggest that multisensory interactions can alter the tuning and gain of arm position-related LFP activity in the SPL.

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