Evidence map›Paper›PMID 33343499›Full record

ArticleFrontiers in neurology2020

Recovery of Theta Frequency Oscillations in Rats Following Lateral Fluid Percussion Corresponds With a Mild Cognitive Phenotype.

Katelynn Ondek, Aleksandr Pevzner, Kayleen Tercovich, Amber M Schedlbauer, Ali Izadi, Arne D Ekstrom, Stephen L Cowen, Kiarash Shahlaie, Gene G Gurkoff

Abstract read
In one paragraph

Article in Frontiers in neurology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Katelynn OndekDepartment of Neurological Surgery, University of California, Davis, Davis, CA, United States.
Aleksandr PevznerDepartment of Neurological Surgery, University of California, Davis, Davis, CA, United States.
Kayleen TercovichDepartment of Neurological Surgery, University of California, Davis, Davis, CA, United States.
Amber M SchedlbauerDepartment of Neurological Surgery, University of California, Davis, Davis, CA, United States.
Ali IzadiDepartment of Neurological Surgery, University of California, Davis, Davis, CA, United States.
Arne D EkstromDepartment of Psychology, The University of Arizona, Tucson, AZ, United States.
Stephen L CowenDepartment of Psychology, The University of Arizona, Tucson, AZ, United States.
Kiarash ShahlaieDepartment of Neurological Surgery, University of California, Davis, Davis, CA, United States.
Gene G GurkoffDepartment of Neurological Surgery, University of California, Davis, Davis, CA, United States.

Funding

Learning, Memory, and Plasticity (LaMP) Training ProgramT32MH112507 · NIMH · UNIVERSITY OF CALIFORNIA AT DAVIS · PI Karen Zito · 2017 to 2026
$2.4M
Restoring functional connectivity following TBIR01NS084026 · NINDS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI GURKOFF, GENE GABRIEL · 2014 to 2018
$2.1M
NIMH NIH HHS T32 MH112507NINDS NIH HHS R01 NS084026
6 · The paper itself

Abstract

Whether from a fall, sports concussion, or even combat injury, there is a critical need to identify when an individual is able to return to play or work following traumatic brain injury (TBI). Electroencephalogram (EEG) and local field potentials (LFP) represent potential tools to monitor circuit-level abnormalities related to learning and memory: specifically, theta oscillations can be readily observed and play a critical role in cognition. Following moderate traumatic brain injury in the rat, lasting changes in theta oscillations coincide with deficits in spatial learning. We hypothesized, therefore, that theta oscillations can be used as an objective biomarker of recovery, with a return of oscillatory activity corresponding with improved spatial learning. In the current study, LFP were recorded from dorsal hippocampus and anterior cingulate in awake, behaving adult Sprague Dawley rats in both a novel environment on post-injury days 3 and 7, and Barnes maze spatial navigation on post-injury days 8-11. Theta oscillations, as measured by power, theta-delta ratio, peak theta frequency, and phase coherence, were significantly altered on day 3, but had largely recovered by day 7 post-injury. Injured rats had a mild behavioral phenotype and were not different from shams on the Barnes maze, as measured by escape latency. Injured rats did use suboptimal search strategies. Combined with our previous findings that demonstrated a correlation between persistent alterations in theta oscillations and spatial learning deficits, these new data suggest that neural oscillations, and particularly theta oscillations, have potential as a biomarker to monitor recovery of brain function following TBI. Specifically, we now demonstrate that oscillations are depressed following injury, but as oscillations recover, so does behavior.

Indexed as

biomarkerin vivo electrophysiologyphase coherencespatial learningtheta oscillationstraumatic brain injury

Identifiers

PMID33343499
PMCPMC7746872

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.