Evidence map›Paper›PMID 25394661›Full record

ArticleAmerican journal of physiology. Gastrointestinal and liver physiology2015

SCFA transport in rat duodenum.

Izumi Kaji, Toshihiko Iwanaga, Masahiko Watanabe, Paul H Guth, Eli Engel, Jonathan D Kaunitz, Yasutada Akiba

Open access · greenAbstract read
In one paragraph

Article in American journal of physiology. Gastrointestinal and liver physiology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
3.5field-weighted citation impact, top 8% 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

40 citing papers in PubMed, 65 citations in OpenAlex.

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  9. [The Relationship of Dysbiosis of Duodenal Microbiome and Functional Dyspepsia].The Korean journal of helicobacter and upper gastrointestinal research · 2024
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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

7 authors at 3 institutions in 2 countries.

Izumi KajiDepartment of Medicine, School of Medicine, University of California, Los Angeles, Los Angeles, California; Department of Anatomy, Hokkaido University Graduate School of Medicine, Sapporo, Japan; and Brentwood Biomedical Research Institute, Los Angeles, California.
Toshihiko IwanagaDepartment of Anatomy, Hokkaido University Graduate School of Medicine, Sapporo, Japan; and.
Masahiko WatanabeDepartment of Anatomy, Hokkaido University Graduate School of Medicine, Sapporo, Japan; and.
Paul H GuthGreater Los Angeles Veterans Affairs Healthcare System, Los Angeles, California; Department of Medicine, School of Medicine, University of California, Los Angeles, Los Angeles, California;
Eli EngelDepartment of Biomathematics, School of Medicine, University of California, Los Angeles, Los Angeles, California;
Jonathan D KaunitzGreater Los Angeles Veterans Affairs Healthcare System, Los Angeles, California; Department of Medicine, School of Medicine, University of California, Los Angeles, Los Angeles, California; Department of Surgery, School of Medicine, University of California, Los Angeles, Los Angeles, California; Brentwood Biomedical Research Institute, Los Angeles, California jake@ucla.edu.
Yasutada AkibaGreater Los Angeles Veterans Affairs Healthcare System, Los Angeles, California; Department of Medicine, School of Medicine, University of California, Los Angeles, Los Angeles, California; Brentwood Biomedical Research Institute, Los Angeles, California.
University of California, Los Angeles · USHokkaido University · JPBrentwood Biomedical Research Institute · US

Funding

Pilot and Feasibility ProgramP30DK041301 · NIDDK · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI ROZENGURT, JUAN ENRIQUE · 1990 to 2019
$18.0M
Duodenal Muscosal Defense MechanismsR01DK054221 · NIDDK · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI KAUNITZ, JONATHAN D. · 1999 to 2016
$4.4M
BLRD VA I01 BX001245NIDDK NIH HHS P30-DK-0413NIDDK NIH HHS P30 DK041301NIDDK NIH HHS R01 DK054221NIDDK NIH HHS R01-DK-54221
6 · The paper itself

Abstract

Bacterial or ingested food-derived short-chain fatty acids (SCFAs) are present in the duodenal lumen. Acetate, the most abundant SCFA in the foregut lumen, is absorbed immediately after ingestion, although the mechanism by which this absorption occurs is not fully understood. We investigated the distribution and function of candidate SCFA transporters in rat duodenum. The Na(+)-coupled monocarboxylate transporter-1 (SMCT1) was localized to the brush border, whereas the pH-dependent monocarboxylate transporter (MCT) 1 and MCT4 were localized to the duodenocyte basolateral membrane. In Ussing chambered duodenal mucosa, luminal acetate dose-dependently increased short-circuit current (Isc) in the presence of serosal bumetanide and indomethacin by a luminal Na(+)-dependent, ouabain-sensitive mechanism. The Isc response was inhibited dose-dependently by the SMCT1 nonsubstrate inhibitor ibuprofen, consistent with net electrogenic absorption of acetate via SMCT1. Other SCFAs and lactate also increased Isc. Furthermore, duodenal loop perfusion of acetate increased portal venous acetate concentration, inhibited by coperfusion of ibuprofen or a MCT inhibitor. Luminal acetate perfusion increased duodenal HCO3 (-) secretion via capsaicin-sensitive afferent nerve activation and cyclooxygenase activity, consistent with absorption-mediated HCO3 (-) secretion. These results suggest that absorption of luminal SCFA via SMCT1 and MCTs increases duodenal HCO3 (-) secretion. In addition to SCFA sensing via free fatty acid receptors, the presence of rapid duodenal SCFA absorption may be important for the suppression of luminal bacterial colonization and implicated in the generation of functional dyspepsia due to bacterial overgrowth.

Indexed as

AnimalsBiological TransportDuodenumFatty Acids, VolatileHydrogen-Ion ConcentrationIntestinal AbsorptionIntestinal MucosaMaleModels, AnimalPropionatesRats, Sprague-DawleySodiumFatty Acids, VolatilePropionatesSodiumacetatemonocarboxylate transportershort-chain fatty acidsodium-coupled monocarboxylate transporter

Identifiers

PMID25394661
PMCPMC4312951
OpenAlexW2054781816

What OpenQuestion holds

Textmetadata
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.