Evidence map›Paper›PMID 38268565›Full record

ReviewFrontiers in psychiatry2023

Colin J McArdle, Alana A Arnone, Chelcie F Heaney, Kimberly F Raab-Graham

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in psychiatry, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 2 pooled it
5.9field-weighted citation impact, top 3% of its field
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

19 citing papers in PubMed, 2 syntheses or guidelines pooled it, 22 citations in OpenAlex.

  1. Psychotherapy and inhibitory control: Insights from fMRI research.Psychiatry and clinical neurosciences · 2026
    Pooled it
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  18. Gut microbiota-mediated pain sensitization: mechanisms and therapeutic implications.Frontiers in pain research (Lausanne, Switzerland) · 2025
    Review
  19. 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

4 authors at 1 institution in 1 country.

Colin J McArdleDepartment of Physiology and Pharmacology, Wake Forest University School of Medicine, Winston-Salem, NC, United States.
Alana A ArnoneDepartment of Physiology and Pharmacology, Wake Forest University School of Medicine, Winston-Salem, NC, United States.
Chelcie F HeaneyDepartment of Physiology and Pharmacology, Wake Forest University School of Medicine, Winston-Salem, NC, United States.
Kimberly F Raab-GrahamDepartment of Physiology and Pharmacology, Wake Forest University School of Medicine, Winston-Salem, NC, United States.
Wake Forest University · US

Funding

Wake Forest University School of Medicine Alzheimer's Disease Research CenterP30AG072947 · NIA · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI SUZANNE CRAFT · 2021 to 2026
$24.3M
Wake Forest Alzheimer's Disease Core CenterP30AG049638 · NIA · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI WILLIAMSON, JEFF DOUGLAS · 2016 to 2020
$12.2M
MULTI-DISCIPLINARY TRAINING IN THE BIOLOGY OF ALCOHOLISMT32AA007565 · NIAAA · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI BRIAN A MCCOOL · 1994 to 2026
$10.1M
Molecular Mechanism of Hippocampal network excitability in a novel, in vivo model of Tuberous Sclerosis ComplexR01NS105005 · NINDS · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI RAAB-GRAHAM, KIMBERLY FRANCES · 2018 to 2022
$1.9M
Biochemical Studies Underlying Acute Ethanol's Antidepressant-like effects during Withdrawal in a Preclinical Model of Ethanol DependenceR01AA029691 · NIAAA · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI Kimberly Frances Raab-Graham · 2023 to 2026
$1.4M
NIAAA NIH HHS R01 AA029691NIAAA NIH HHS T32 AA007565NIA NIH HHS P30 AG049638NIA NIH HHS P30 AG072947NINDS NIH HHS R01 NS105005
6 · The paper itself

Abstract

Gamma-aminobutyric acid (GABA) is the primary inhibitory neurotransmitter in the central nervous system. In the mature brain, inhibitory GABAergic signaling is critical in maintaining neuronal homeostasis and vital human behaviors such as cognition, emotion, and motivation. While classically known to inhibit neuronal function under physiological conditions, previous research indicates a paradoxical switch from inhibitory to excitatory GABAergic signaling that is implicated in several neurological disorders. Various mechanisms have been proposed to contribute to the excitatory switch such as chloride ion dyshomeostasis, alterations in inhibitory receptor expression, and modifications in GABAergic synaptic plasticity. Of note, the hypothesized mechanisms underlying excitatory GABAergic signaling are highlighted in a number of neurodevelopmental, substance use, stress, and neurodegenerative disorders. Herein, we present an updated review discussing the presence of excitatory GABAergic signaling in various neurological disorders, and their potential contributions towards disease pathology.

Indexed as

depolarizingdiseasesexcitatoryGABAGABAARsneurological

Identifiers

PMID38268565
PMCPMC10805837
OpenAlexW4390699074

What OpenQuestion 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 OpenQuestion graph.