Evidence map›Paper›PMID 19496086›Full record

ArticleMolecular nutrition & food research2009

Dietary procyanidins enhance transcriptional activity of bile acid-activated FXR in vitro and reduce triglyceridemia in vivo in a FXR-dependent manner.

Josep Maria Del Bas, Marie-Louise Ricketts, Montserrat Vaqué, Esther Sala, Helena Quesada, Anna Ardevol, M Josepa Salvadó, Mayte Blay, Lluís Arola, David D Moore and 3 more

Abstract read
In one paragraph

Article in Molecular nutrition & food research, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed, 3 pooled it
3.0field-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

38 citing papers in PubMed, 3 syntheses or guidelines pooled it, 89 citations in OpenAlex.

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  8. A review of alpha-glucosidase inhibitors from plants as potential candidates for the treatment of type-2 diabetes.Phytochemistry reviews : proceedings of the Phytochemical Society of Europe · 2022
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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 2 institutions in 2 countries.

Josep Maria Del BasDepartament de Bioquímica i Biotecnología, Universitat Rovira i Virgili, Campus Sescelades, Tarragona, Spain.
Marie-Louise Ricketts
Montserrat Vaqué
Esther Sala
Helena Quesada
Anna Ardevol
M Josepa Salvadó
Mayte Blay
Lluís Arola
David D Moore
Gerard Pujadas
Juan Fernandez-Larrea
Cinta Bladé
Universidad Rovira i Virgili · ESBaylor College of Medicine · US

Funding

RETINOID SIGNALING BY A NEW NUCLEAR HORMONE RECEPTORR01DK053366 · NIDDK · BAYLOR COLLEGE OF MEDICINE · PI MOORE, DAVID D · 1998 to 2006
$2.0M
NIDDK NIH HHS R01 DK053366
6 · The paper itself

Abstract

Consumption of dietary flavonoids has been associated with reduced mortality and risk of cardiovascular disease, partially by reducing triglyceridemia. We have previously reported that a grape seed procyanidin extract (GSPE) reduces postprandial triglyceridemia in normolipidemic animals signaling through the orphan nuclear receptor small heterodimer partner (SHP) a target of the bile acid receptor farnesoid X receptor (FXR). Our aim was to elucidate whether FXR mediates the hypotriglyceridemic effect of procyanidins. In FXR-driven luciferase expression assays GSPE dose-dependently enhanced FXR activity in the presence of chenodeoxycholic acid. GSPE gavage reduced triglyceridemia in wild type mice but not in FXR-null mice, revealing FXR as an essential mediator of the hypotriglyceridemic actions of procyanidins in vivo. In the liver, GSPE downregulated, in an FXR-dependent manner, the expression of the transcription factor steroid response element binding protein 1 (SREBP1) and several SREBP1 target genes involved in lipogenesis, and upregulated ApoA5 expression. Altogether, our results indicate that procyanidins lower triglyceridemia following the same pathway as bile acids: activation of FXR, transient upregulation of SHP expression and subsequent downregulation of SREBP1 expression. This study adds dietary procyanidins to the arsenal of FXR ligands with potential therapeutic use to combat hypertriglyceridemia, type 2 diabetes and metabolic syndrome.

Indexed as

AnimalsBile Acids and SaltsChlorocebus aethiopsGrape Seed ExtractHumansHypertriglyceridemiaMiceMice, Inbred C57BLPlant ExtractsProanthocyanidinsReceptor, Farnesoid X-ActivatedReceptors, Cytoplasmic and NuclearSterol Regulatory Element Binding Protein 1Transcription, GeneticBile Acids and SaltsGrape Seed ExtractGrape Seed ProanthocyanidinsPlant ExtractsProanthocyanidinsReceptor, Farnesoid X-ActivatedReceptors, Cytoplasmic and NuclearSterol Regulatory Element Binding Protein 1

Identifiers

PMID19496086
PMCPMC4142053
OpenAlexW2093128178

What OpenQuestion holds

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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.