Evidence map›Paper›PMID 36106538›Full record

ArticleFASEB journal : official publication of the Federation of American Societies for Experimental Biology2022

The intestine is a major contributor to circulating succinate in mice.

Wenxin Tong, Sarah A Hannou, You Wang, Inna Astapova, Ashot Sargsyan, Ruby Monn, Venkataramana Thiriveedi, Diana Li, Jessica R McCann, John F Rawls and 3 more

Open access · greenAbstract read
In one paragraph

Article in FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.0field-weighted citation impact, top 13% 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

18 citing papers in PubMed, 23 citations in OpenAlex.

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  12. Observational
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  15. Metabolites as signalling molecules.Nature reviews. Molecular cell biology · 2023
    Review
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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

13 authors at 1 institution in 1 country.

Wenxin TongDepartment of Pharmacology and Cancer Biology, Duke University, Durham, North Carolina, USA.
Sarah A HannouDuke Molecular Physiology Institute, Duke University, Durham, North Carolina, USA.
You WangDuke Molecular Physiology Institute, Duke University, Durham, North Carolina, USA.
Inna AstapovaDuke Molecular Physiology Institute, Duke University, Durham, North Carolina, USA.
Ashot SargsyanDuke Molecular Physiology Institute, Duke University, Durham, North Carolina, USA.
Ruby MonnDuke Molecular Physiology Institute, Duke University, Durham, North Carolina, USA.
Venkataramana ThiriveediDivision of Gastroenterology, Duke University, Durham, North Carolina, USA.
Diana LiDivision of Gastroenterology, Duke University, Durham, North Carolina, USA.
Jessica R McCannDepartment of Molecular Genetics and Microbiology, Duke Microbiome Center, Duke University, Durham, North Carolina, USA.
John F RawlsDepartment of Molecular Genetics and Microbiology, Duke Microbiome Center, Duke University, Durham, North Carolina, USA.
Jatin RoperDepartment of Pharmacology and Cancer Biology, Duke University, Durham, North Carolina, USA.
Guo-Fang ZhangDuke Molecular Physiology Institute, Duke University, Durham, North Carolina, USA.
Mark A HermanDuke Molecular Physiology Institute, Duke University, Durham, North Carolina, USA.ORCID https://orcid.org/0000-0001-6979-103X
Duke University · US

Funding

Pilot & Feasibility ProgramP30DK124723 · NIDDK · WAKE FOREST UNIVERSITY HEALTH SCIENCES · PI P Darrell Neufer · 2020 to 2026
$11.0M
The Role of ChREBP in Fructose Induced Metabolic DiseaseR01DK100425 · NIDDK · DUKE UNIVERSITY · PI HERMAN, MARK A · 2014 to 2023
$3.6M
Mechanisms connecting dysregulated BCAA, glucose & lipid metabolism in the pathogenesis of metabolic diseaseR01DK121710 · NIDDK · DUKE UNIVERSITY · PI HERMAN, MARK A, NEWGARD, CHRISTOPHER B · 2019 to 2022
$2.7M
NIDDK NIH HHS P30 DK124723NIDDK NIH HHS R01 DK100425NIDDK NIH HHS R01 DK121710
6 · The paper itself

Abstract

The tricarboxylic acid (TCA) cycle is the epicenter of cellular aerobic metabolism. TCA cycle intermediates facilitate energy production and provide anabolic precursors, but also function as intra- and extracellular metabolic signals regulating pleiotropic biological processes. Despite the importance of circulating TCA cycle metabolites as signaling molecules, the source of circulating TCA cycle intermediates remains uncertain. We observe that in mice, the concentration of TCA cycle intermediates in the portal blood exceeds that in tail blood indicating that the gut is a major contributor to circulating TCA cycle metabolites. With a focus on succinate as a representative of a TCA cycle intermediate with signaling activities and using a combination of gut microbiota depletion mouse models and isotopomer tracing, we demonstrate that intestinal microbiota is not a major contributor to circulating succinate. Moreover, we demonstrate that endogenous succinate production is markedly higher than intestinal succinate absorption in normal physiological conditions. Altogether, these results indicate that endogenous succinate production within the intestinal tissue is a major physiological source of circulating succinate. These results provide a foundation for an investigation into the role of the intestine in regulating circulating TCA cycle metabolites and their potential signaling effects on health and disease.

Indexed as

Gastrointestinal MicrobiomeSuccinic AcidAnimalsCitric Acid CycleIntestinesMiceSuccinatesSuccinatesSuccinic Acidcirculating biomarkersintestinesuccinateTCA cycle intermediates

Identifiers

PMID36106538
PMCPMC9523828
OpenAlexW4295907356

What Socratic holds

Textmetadata
LicenceTDM
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.