Evidence map›Paper›PMID 26051626›Full record

ArticleScientific reports2015

Dietary proanthocyanidins modulate BMAL1 acetylation, Nampt expression and NAD levels in rat liver.

Aleix Ribas-Latre, Laura Baselga-Escudero, Ester Casanova, Anna Arola-Arnal, M-Josepa Salvadó, Cinta Bladé, Lluís Arola

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed, 1 pooled it
2.3field-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

28 citing papers in PubMed, 1 synthesis or guideline pooled it, 58 citations in OpenAlex.

  1. Pooled it
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  14. A wrinkle in time: circadian biology in pulmonary vascular health and disease.American journal of physiology. Lung cellular and molecular physiology · 2022
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  19. Molecules (Basel, Switzerland) · 2019
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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 1 institution in 1 country.

Aleix Ribas-LatreNutrigenomic Research Group. Department of Biochemistry and Biotechnology, Universitat Rovira i Virgili, Tarragona, Spain.
Laura Baselga-EscuderoNutrigenomic Research Group. Department of Biochemistry and Biotechnology, Universitat Rovira i Virgili, Tarragona, Spain.
Ester CasanovaNutrigenomic Research Group. Department of Biochemistry and Biotechnology, Universitat Rovira i Virgili, Tarragona, Spain.
Anna Arola-ArnalNutrigenomic Research Group. Department of Biochemistry and Biotechnology, Universitat Rovira i Virgili, Tarragona, Spain.
M-Josepa SalvadóNutrigenomic Research Group. Department of Biochemistry and Biotechnology, Universitat Rovira i Virgili, Tarragona, Spain.
Cinta BladéNutrigenomic Research Group. Department of Biochemistry and Biotechnology, Universitat Rovira i Virgili, Tarragona, Spain.
Lluís ArolaNutrigenomic Research Group. Department of Biochemistry and Biotechnology, Universitat Rovira i Virgili, Tarragona, Spain.
Universidad Rovira i Virgili · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Metabolism follows circadian rhythms, which are driven by peripheral clocks. Clock genes in the liver are entrained by daytime meals and food components. Proanthocyanidins (PAs), the most abundant flavonoids in the human diet, modulate lipid and glucose metabolism. The aim of this study was to determine whether PAs could adjust the clock system in the liver. Male Wistar rats were orally gavaged with 250 mg grape seed proanthocyanidin extract (GSPE)/kg body weight at zeitgeber time (ZT) 0 (light turned on), at ZT12 (light turned off), or before a 6 hour jet-lag and sacrificed at different times. The 24 hour rhythm of clock-core and clock-controlled gene expression indicated that nicotinamide phosphoribosyltransferase (Nampt) was the most sensitive gene to GSPE. However, Nampt was repressed or overexpressed after GSPE administration at ZT0 or ZT12, respectively. NAD levels, which are controlled by Nampt and also exhibit circadian rhythm, decreased or increased according to Nampt expression. Moreover, the ratio of acetylated Bmal1, that directly drives Nampt expression, only increased when GSPE was administered at ZT12. Therefore, GSPE modulated the clock system in the liver, suggesting that PAs can regulate lipid and glucose metabolism by adjusting the circadian rhythm in the liver.

Indexed as

AcetylationAnimalsARNTL Transcription FactorsCircadian RhythmCytokinesGene Expression Regulation, DevelopmentalGlucoseHumansLipid MetabolismLiverMaleMiceNADNicotinamide PhosphoribosyltransferaseProanthocyanidinsRatsArntl protein, ratARNTL Transcription FactorsCytokinesGlucoseNADNicotinamide Phosphoribosyltransferasenicotinamide phosphoribosyltransferase, ratproanthocyanidinProanthocyanidins

Identifiers

PMID26051626
PMCPMC4603780
OpenAlexW588563159

What OpenQuestion holds

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LicenceCC BY
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.