Evidence map›Paper›PMID 35999325›Full record

ReviewMolecular neurobiology2022

A Pattern to Link Adenosine Signaling, Circadian System, and Potential Final Common Pathway in the Pathogenesis of Major Depressive Disorder.

Xin-Ling Wang, Wilf Gardner, Shu-Yan Yu, Tsvetan Serchov

Open access · hybridAbstract readReview
In one paragraph

Review in Molecular neurobiology, 2022. 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
1.1field-weighted citation impact, top 27% 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

3 citing papers in PubMed, 10 citations in OpenAlex.

  1. The crosstalk between CREB and PER2 mediates the transition between mania- and depression-like behavior.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2025
    Article
  2. Article
  3. Review
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 3 institutions in 3 countries.

Xin-Ling WangSchool of Basic Medical Sciences, Cheeloo College of Medicine, Shandong University, Ji'nan, 250012, Shandong, China.
Wilf GardnerCentre National de La Recherche Scientifique, Université de Strasbourg, Institut Des Neurosciences Cellulaires Et Intégratives, 67000, Strasbourg, France.
Shu-Yan YuSchool of Basic Medical Sciences, Cheeloo College of Medicine, Shandong University, Ji'nan, 250012, Shandong, China. shuyanyu@sdu.edu.cn.
Tsvetan SerchovCentre National de La Recherche Scientifique, Université de Strasbourg, Institut Des Neurosciences Cellulaires Et Intégratives, 67000, Strasbourg, France. tsvetan.serchov@uniklinik-freiburg.de.ORCID http://orcid.org/0000-0002-2234-2875
Shandong University · CNInstitut des Neurosciences Cellulaires et Intégratives · FRUniversity Medical Center Freiburg · DE

Funding

Deutsche Forschungsgemeinschaft SE2666/2-3Fondation pour la Recherche Médicale AJE201912009450Fundamental Research Fund of Shandong University 2020GN095National Natural Science Foundation of China NSFC81873796National Natural Science Foundation of China NSFC82071513Natural Science Foundation of Shandong Province ZR2021QH282Université de Strasbourg 2020-035
6 · The paper itself

Abstract

Several studies have reported separate roles of adenosine receptors and circadian clockwork in major depressive disorder. While less evidence exists for regulation of the circadian clock by adenosine signaling, a small number of studies have linked the adenosinergic system, the molecular circadian clock, and mood regulation. In this article, we review relevant advances and propose that adenosine receptor signaling, including canonical and other alternative downstream cellular pathways, regulates circadian gene expression, which in turn may underlie the pathogenesis of mood disorders. Moreover, we summarize the convergent point of these signaling pathways and put forward a pattern by which Homer1a expression, regulated by both cAMP-response element binding protein (CREB) and circadian clock genes, may be the final common pathogenetic mechanism in depression.

Indexed as

Circadian ClocksMajor Depressive DisorderAdenosineCircadian RhythmHumansMood DisordersReceptors, Purinergic P1AdenosineReceptors, Purinergic P1Adenosine receptorsCircadian genesCREBDepressionHomer1a

Identifiers

PMID35999325
PMCPMC9525429
OpenAlexW4292767419

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.