Evidence map›Paper›PMID 39268032›Full record

ArticleFrontiers in neuroscience2024

Early hippocampal high-amplitude rhythmic spikes predict post-traumatic epilepsy in mice.

Tyler Shannon, Noah Levine, Rina Dirickson, Yuyan Shen, Christopher Cotter, Noora Rajjoub, Julie Fitzgerald, Fernando Pardo-Manuel de Villena, Olga Kokiko-Cochran, Bin Gu

Abstract read
In one paragraph

Article in Frontiers in neuroscience, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors.

Tyler ShannonDepartment of Neuroscience, Ohio State University, Columbus, OH, United States.
Noah LevineElectrical and Computer Engineering Program, Ohio State University, Columbus, OH, United States.
Rina DiricksonDepartment of Neuroscience, Ohio State University, Columbus, OH, United States.
Yuyan ShenCollege of Veterinary Medicine, Ohio State University, Columbus, OH, United States.
Christopher CotterDepartment of Neuroscience, Ohio State University, Columbus, OH, United States.
Noora RajjoubDepartment of Neuroscience, Ohio State University, Columbus, OH, United States.
Julie FitzgeraldDepartment of Neuroscience, Ohio State University, Columbus, OH, United States.
Fernando Pardo-Manuel de VillenaDepartment of Genetics, University of North Carolina, Chapel Hill, NC, United States.
Olga Kokiko-CochranDepartment of Neuroscience, Ohio State University, Columbus, OH, United States.
Bin GuDepartment of Neuroscience, Ohio State University, Columbus, OH, United States.

Funding

Characterizing Sleep Disruption as a Post-Injury Immune StressorR01NS109585 · NINDS · OHIO STATE UNIVERSITY · PI KOKIKO-COCHRAN, OLGA NICOLE · 2019 to 2023
$2.1M
NINDS NIH HHS R01 NS109585
6 · The paper itself

Abstract

Oscillations, a highly conserved brain function across mammalian species, play a pivotal role in both brain physiology and pathology. Traumatic brain injury (TBI) frequently results in subacute and chronic alterations in brain oscillations, which are often associated with complications like post-traumatic epilepsy (PTE) in patients and animal models. We recently conducted longitudinal recordings of local field potential from the contralateral hippocampus of 12 strains of recombinant inbred Collaborative Cross (CC) mice and classical laboratory inbred C57BL/6 J mice after lateral fluid percussion injury. In this study, we profiled the acute (<12 h post-injury) and subacute (12-48 h post-injury) hippocampal oscillatory responses to TBI and evaluated their predictive value for PTE. We found dynamic high-amplitude rhythmic spikes with elevated power density and reduced signal complexity that prevailed exclusively during the acute phase in CC031 mice, which later developed PTE. This characteristic early brain oscillatory alteration was absent in CC031 sham controls, as well as in other CC strains and reference C57BL/6 J mice that did not develop PTE after TBI. Our findings offer quantitative measures linking early hippocampal brain oscillation to PTE at a population level in mice. These insights enhance understanding of circuit mechanisms and suggest potential targets for neuromodulatory intervention.

Indexed as

biomarkersbrain oscillationcollaborative cross miceEEGepilepsylocal field potential (LFP)post traumatic epilepsytraumatic brain injury

Identifiers

PMID39268032
PMCPMC11390562

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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 Socratic graph.