Evidence map›Paper›PMID 40656063›Full record

ReviewNeuroscience applied2024

Coping with the multifaceted and multifunctional role of cortisol in the brain.

Edo Ronald de Kloet

Abstract readReview
In one paragraph

Review in Neuroscience applied, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
  4. Observational
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

1 author.

Edo Ronald de KloetLeiden University Medical Center, Department of Clinical Medicine, Division of Endocrinology, Leiden University, Leiden, the Netherlands.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glucocorticoid hormones cortisol and corticosterone (collectively called CORT), secreted as the end products of the hypothalamus-pituitary-adrenal (HPA)-axis, coordinate body and brain function over the circadian cycle and during adaptation to stress. For this purpose, the hormones bind to the mineralocorticoid receptors (MR) with the highest expression in the hippocampus/lateral septum neurons and a 10-fold lower affinity to the widely distributed glucocorticoid receptors (GR). MR and GR mediate opposing rapid non-genomic actions of CORT on neuronal excitability. MR and GR also mediate in a slower complementary manner the genomic actions on neuronal excitability, the management of energy resources, the control of defense reactions, and emotional, motivational, social, and valuation processes to gain control and adapt. The glucocorticoids perform this life-sustaining pleiotropic action in interaction with the neuropeptides of the HPA-axis, the central and autonomic nervous systems, and the immune system. Here, the progress is discussed in (i) detecting dysregulation and recovery in glucocorticoid secretion patterns, (ii) unraveling the complementary function of MR and GR in the mechanism underlying stress-coping and adaptation, and (iii) applying selective CORT receptor modulators for attenuating neurodegeneration and enhancing resilience.

Indexed as

AdaptationAmygdalaBrainGlucocorticoid receptorsHippocampusMineralocorticoid receptorsStress

Identifiers

PMID40656063
PMCPMC12244002

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.