Evidence map›Paper›PMID 24929099›Full record

ReviewFrontiers in neuroendocrinology2015

GABAA receptor-acting neurosteroids: a role in the development and regulation of the stress response.

Benjamin G Gunn, Linda Cunningham, Scott G Mitchell, Jerome D Swinny, Jeremy J Lambert, Delia Belelli

Open access · hybridAbstract readReview
In one paragraph

Review in Frontiers in neuroendocrinology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 61 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
61citing papers in PubMed, 2 pooled it
4.6field-weighted citation impact, top 4% 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

61 citing papers in PubMed, 2 syntheses or guidelines pooled it, 152 citations in OpenAlex.

  1. Pooled it
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  14. Why Can Modulation of α6-Containing GABAArchives of pharmacology and therapeutics · 2024
    Article
  15. Neurosteroid Receptor Modulators for Treating Traumatic Brain Injury.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2023
    Review
  16. Prefrontal allopregnanolone mediates the adverse effects of acute stress in a mouse model of tic pathophysiology.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2023
    Article
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1 more citing papers are in PubMed but not listed here.

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 at 3 institutions in 1 country.

Benjamin G GunnDivision of Neuroscience, Medical Research Institute, Dundee University, Ninewells Hospital and Medical School, Dundee DD1 9SY, UK.
Linda CunninghamDivision of Neuroscience, Medical Research Institute, Dundee University, Ninewells Hospital and Medical School, Dundee DD1 9SY, UK.
Scott G MitchellDivision of Neuroscience, Medical Research Institute, Dundee University, Ninewells Hospital and Medical School, Dundee DD1 9SY, UK.
Jerome D SwinnyInstitute for Biomedical and Biomolecular Sciences, School of Pharmacy and Biomedical Sciences, University of Portsmouth, UK.
Jeremy J LambertDivision of Neuroscience, Medical Research Institute, Dundee University, Ninewells Hospital and Medical School, Dundee DD1 9SY, UK.
Delia BelelliDivision of Neuroscience, Medical Research Institute, Dundee University, Ninewells Hospital and Medical School, Dundee DD1 9SY, UK. Electronic address: d.belelli@dundee.ac.uk.
Ninewells Hospital · GBUniversity of Dundee · GBUniversity of Portsmouth · GB

Funding

Biotechnology and Biological Sciences Research Council 11426Medical Research Council MR/K500896/1
6 · The paper itself

Abstract

Regulation of hypothalamic-pituitary-adrenocortical (HPA) axis activity by stress is a fundamental survival mechanism and HPA-dysfunction is implicated in psychiatric disorders. Adverse early life experiences, e.g. poor maternal care, negatively influence brain development and programs an abnormal stress response by encoding long-lasting molecular changes, which may extend to the next generation. How HPA-dysfunction leads to the development of affective disorders is complex, but may involve GABAA receptors (GABAARs), as they curtail stress-induced HPA axis activation. Of particular interest are endogenous neurosteroids that potently modulate the function of GABAARs and exhibit stress-protective properties. Importantly, neurosteroid levels rise rapidly during acute stress, are perturbed in chronic stress and are implicated in the behavioural changes associated with early-life adversity. We will appraise how GABAAR-active neurosteroids may impact on HPA axis development and the orchestration of the stress-evoked response. The significance of these actions will be discussed in the context of stress-associated mood disorders.

Indexed as

HumansHypothalamo-Hypophyseal SystemNeurotransmitter AgentsPituitary-Adrenal SystemReceptors, GABA-AStress, PsychologicalNeurotransmitter AgentsReceptors, GABA-AAllopregnanoloneDepressionEarly-life stressGABA(A) receptorHPA axis

Identifiers

PMID24929099
PMCPMC4349499
OpenAlexW2113668852

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.