Evidence map›Paper›PMID 21350192›Full record

ArticleAmerican journal of physiology. Gastrointestinal and liver physiology2011

Different functions of intestinal and liver-type fatty acid-binding proteins in intestine and in whole body energy homeostasis.

William Stacy Lagakos, Angela Marie Gajda, Luis Agellon, Bert Binas, Victor Choi, Bernadette Mandap, Timothy Russnak, Yin Xiu Zhou, Judith Storch

Open access · greenAbstract read
In one paragraph

Article in American journal of physiology. Gastrointestinal and liver physiology, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 53 papers.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed
3.6field-weighted citation impact, top 6% 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

53 citing papers in PubMed, 81 citations in OpenAlex.

  1. Article
  2. Polyunsaturated fatty acid metabolism in the retinal pigment epithelium and its association with outer retinal disease.Mammalian genome : official journal of the International Mammalian Genome Society · 2026
    Review
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  19. Frontiers in microbiology · 2022
    Article
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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

9 authors at 3 institutions in 3 countries.

William Stacy LagakosDepartment of Nutritional Sciences, Rutgers, the State University of New Jersey, New Brunswick, USA.
Angela Marie Gajda
Luis Agellon
Bert Binas
Victor Choi
Bernadette Mandap
Timothy Russnak
Yin Xiu Zhou
Judith Storch
Rutgers, The State University of New Jersey · USHanyang University · KRMcGill University · CA

Funding

Supplement to DK-38389 Lipid Transport in the IntestineR01DK038389 · NIDDK · RUTGERS THE ST UNIV OF NJ NEW BRUNSWICK · PI SAMPATH, HARINI, STORCH, JUDITH · 1992 to 2025
$8.6M
FATTY ACID ASSIMILATION IN THE INTESTINER29DK038389 · NIDDK · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI STORCH, JUDITH · 1987 to 1991
–
NIDDK NIH HHS DK-38389NIDDK NIH HHS R01 DK038389
6 · The paper itself

Abstract

It has long been known that mammalian enterocytes coexpress two members of the fatty acid-binding protein (FABP) family, the intestinal FABP (IFABP) and the liver FABP (LFABP). Both bind long-chain fatty acids and have similar though not identical distributions in the intestinal tract. While a number of in vitro properties suggest the potential for different functions, the underlying reasons for expression of both proteins in the same cells are not known. Utilizing mice genetically lacking either IFABP or LFABP, we directly demonstrate that each of the enterocyte FABPs participates in specific pathways of intestinal lipid metabolism. In particular, LFABP appears to target fatty acids toward oxidative pathways and dietary monoacylglycerols toward anabolic pathways, while IFABP targets dietary fatty acids toward triacylglycerol synthesis. The two FABP-null models also displayed differences in whole body response to fasting, with LFABP-null animals losing less fat-free mass and IFABP-null animals losing more fat mass relative to wild-type mice. The metabolic changes observed in both null models appear to occur by nontranscriptional mechanisms, supporting the hypothesis that the enterocyte FABPs are specifically trafficking their ligands to their respective metabolic fates.

Indexed as

AnimalsBlotting, WesternBody CompositionBody WeightEatingEnergy MetabolismEnterocytesFatty Acid-Binding ProteinsFatty AcidsFecesGene ExpressionGenotypeHomeostasisIntestinal MucosaIntestinesLipid MetabolismFatty Acid-Binding ProteinsFatty AcidsLipids

Identifiers

PMID21350192
PMCPMC3094135
OpenAlexW2144113979

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.