Evidence map›Paper›PMID 41144291›Full record

ArticleJournal of visualized experiments : JoVE2025

A Cost-Effective and Minimally Invasive Protocol for Chronic Multi-Site Electroencephalography Recording in Freely Moving Mice.

Kazi Rafsan Radeen, Khadijah Shanazz, Caili Hao, Danielle Lauren Weiss, David T Blake, Xingjun Fan

Abstract readVideo-Audio Media
In one paragraph

Article in Journal of visualized experiments : JoVE, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Article
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

6 authors.

Kazi Rafsan Radeen *Department of Cellular Biology and Anatomy, Medical College of Georgia at Augusta University; National Institute of Biotechnology.
Khadijah Shanazz *Department of Neuroscience and Regenerative Medicine, Medical College of Georgia at Augusta University.
Caili HaoDepartment of Cellular Biology and Anatomy, Medical College of Georgia at Augusta University.
Danielle Lauren WeissDepartment of Neurology, Medical College of Georgia at Augusta University.
David T BlakeDepartment of Neuroscience and Regenerative Medicine, Medical College of Georgia at Augusta University; DBLAKE@augusta.edu.
Xingjun FanDepartment of Cellular Biology and Anatomy, Medical College of Georgia at Augusta University; xfan@augusta.edu.

Funding

Primate model of deep brain stimulation for Alzheimers and age-related cognitivedeclineRF1AG060754 · NIA · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI BLAKE, DAVID T, CONSTANTINIDIS, CHRISTOS · 2019 to 2019
$3.9M
Module 3: Gene Expression/ProteomicsP30EY031631 · NEI · AUGUSTA UNIVERSITY · PI Xingjun Fan · 2020 to 2026
$3.6M
Mechanisms and consequences of impaired glutathione homeostasis in the aging Lens.R01EY028158 · NEI · CASE WESTERN RESERVE UNIVERSITY · PI Xingjun Fan · 2018 to 2026
$3.1M
Mechanisms of lens epithelium fibrosis and its relevance to posterior capsule opacificationR01EY032488 · NEI · AUGUSTA UNIVERSITY · PI Xingjun Fan · 2022 to 2026
$1.9M
Cholinergic influence on visual cognitive processingR01EY036089 · NEI · VANDERBILT UNIVERSITY · PI David T Blake, CHRISTOS CONSTANTINIDIS · 2025 to 2026
$1.3M
NEI NIH HHS P30 EY031631NEI NIH HHS R01 EY028158NEI NIH HHS R01 EY032488NEI NIH HHS R01 EY036089NIA NIH HHS RF1 AG060754
6 · The paper itself

Abstract

Electroencephalography (EEG) serves as a fundamental tool for tracking electrical activity in the brain and has become increasingly important in both clinical diagnostics and preclinical animal research. While rodent EEG offers a powerful platform for modeling human neurological disorders, long-term recordings are often limited by the high cost, invasiveness, or technical complexity of existing systems. Here, we present a reliable, accessible, economically viable, and minimally intrusive protocol for chronic, multi-site cortical EEG acquisition in freely moving mice. The technique involves fabricating platinum-iridium wires with screw electrodes connected to a universal serial bus (USB)-type interface, which are anchored epidurally using bone screws and secured with adhesive and dental cement. The system allows for stable signal capture over several months, as demonstrated in wild-type C57BL/6J mice with an 85% post-operative survival rate (n = 20). EEG was sampled at 1,000 Hz and filtered between 1 Hz and 500 Hz using a differential amplifier setup. To validate the system, pentylenetetrazol (20 mg/kg) was administered to induce seizure-like activity, leading to a marked increase in interictal discharges-from 2-5 at baseline to 20-51 events post-injection-accompanied by increased signal amplitude. Discharges were identified based on waveform morphology and signal characteristics matching recognized electrophysiological criteria. The setup is compatible with behavioral video tracking and open-source analysis pipelines, and supports integration with pharmacological, genetic, or neuromodulation studies. This method provides a stable and adaptable platform for investigating brain network dynamics in rodent models, with applications in epilepsy research and beyond.

Indexed as

ElectroencephalographyAnimalsCost-Benefit AnalysisMaleMiceMice, Inbred C57BLPentylenetetrazoleSeizuresPentylenetetrazole

Identifiers

PMID41144291
PMCPMC13128300

What OpenQuestion holds

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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 OpenQuestion graph.