Evidence map›Paper›PMID 37128607›Full record

ArticleiScience2023

N-arachidonylglycine is a caloric state-dependent circulating metabolite which regulates human CD4

Allison M Meadows, Kim Han, Komudi Singh, Antonio Murgia, Ben D McNally, James A West, Rebecca D Huffstutler, Tiffany M Powell-Wiley, Yvonne Baumer, Julian L Griffin and 1 more

Open access · goldAbstract read
In one paragraph

Article in iScience, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.8field-weighted citation impact, top 16% 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

11 citing papers in PubMed, 10 citations in OpenAlex.

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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

11 authors at 4 institutions in 2 countries.

Allison M MeadowsLaboratory of Mitochondrial Biology and Metabolism, NHLBI, NIH, Bethesda, MD, USA.
Kim HanLaboratory of Mitochondrial Biology and Metabolism, NHLBI, NIH, Bethesda, MD, USA.
Komudi SinghLaboratory of Mitochondrial Biology and Metabolism, NHLBI, NIH, Bethesda, MD, USA.
Antonio MurgiaDepartment of Biochemistry and Cambridge Systems Biology Centre, University of Cambridge, Cambridge, UK.
Ben D McNallyDepartment of Biochemistry and Cambridge Systems Biology Centre, University of Cambridge, Cambridge, UK.
James A WestDepartment of Biochemistry and Cambridge Systems Biology Centre, University of Cambridge, Cambridge, UK.
Rebecca D HuffstutlerCardiovascular Branch, NHLBI, NIH, Bethesda, MD, USA.
Tiffany M Powell-WileySocial Determinants of Obesity and Cardiovascular Risk Laboratory, NHLBI, NIH, Bethesda, MD, USA.
Yvonne BaumerSocial Determinants of Obesity and Cardiovascular Risk Laboratory, NHLBI, NIH, Bethesda, MD, USA.
Julian L GriffinDepartment of Biochemistry and Cambridge Systems Biology Centre, University of Cambridge, Cambridge, UK.
Michael N SackLaboratory of Mitochondrial Biology and Metabolism, NHLBI, NIH, Bethesda, MD, USA.
National Institutes of Health · USUniversity of Cambridge · GBNational Heart Lung and Blood Institute · USUniversity of Aberdeen · GB

Funding

Cardiovascular Health and Needs Assessment in Washington D.C.ZIAHL006168 · NHLBI · NATIONAL HEART, LUNG, AND BLOOD INSTITUTE · PI POWELL-WILEY, TIFFANY · 2013 to 2025
$8.1M
6 · The paper itself

Abstract

Caloric deprivation interventions such as intermittent fasting and caloric restriction ameliorate metabolic and inflammatory disease. As a human model of caloric deprivation, a 24-h fast blunts innate and adaptive immune cell responsiveness relative to the refed state. Isolated serum at these time points confers these same immunomodulatory effects on transformed cell lines. To identify serum mediators orchestrating this, metabolomic and lipidomic analysis was performed on serum extracted after a 24-h fast and re-feeding. Bioinformatic integration with concurrent peripheral blood mononuclear cells RNA-seq analysis implicated key metabolite-sensing GPCRs in fasting-mediated immunomodulation. The putative GPR18 ligand N-arachidonylglycine (NAGly) was elevated during fasting and attenuated CD4

Indexed as

Human metabolismImmunologyLipidomicsMetabolomicsTranscriptomics

Identifiers

PMID37128607
PMCPMC10148119
OpenAlexW4362676615

What Socratic 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 Socratic graph.