Evidence map›Paper›PMID 42747643›Full record

ArticleJournal of physiology and biochemistry2026

Chronic administration of a calafate (Berberis microphylla) polyphenol-rich extract modulates gut microbiota and metabolic homeostasis associated with thermogenic activation in high-fat diet-fed mice.

Lissette Duarte, Vanessa Villanueva, Robert Barroux, Juan Francisco Orellana, Denisse Uribe, Javier J Quezada, Luisa Amanda Ramirez, Karla Vasquez, Carlos Poblete-Aro, Martin Gotteland and 3 more

Abstract read
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In one paragraph

Article in Journal of physiology and biochemistry, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Lissette DuarteDepartamento de Nutricion, Facultad de Medicina, Universidad de Chile, Independencia 1027, Santiago, Chile.
Vanessa VillanuevaDepartamento de Nutricion, Facultad de Medicina, Universidad de Chile, Independencia 1027, Santiago, Chile.
Robert BarrouxDepartamento de Nutricion, Facultad de Medicina, Universidad de Chile, Independencia 1027, Santiago, Chile.
Juan Francisco OrellanaDepartamento de Nutricion, Facultad de Medicina, Universidad de Chile, Independencia 1027, Santiago, Chile.
Denisse UribeDepartamento de Nutricion, Facultad de Medicina, Universidad de Chile, Independencia 1027, Santiago, Chile.
Javier J QuezadaDepartamento de Nutricion, Facultad de Medicina, Universidad de Chile, Independencia 1027, Santiago, Chile.
Luisa Amanda RamirezDepartamento de Nutricion, Facultad de Medicina, Universidad de Chile, Independencia 1027, Santiago, Chile.
Karla VasquezDepartamento de Nutricion, Facultad de Medicina, Universidad de Chile, Independencia 1027, Santiago, Chile.
Carlos Poblete-AroFacultad de Ciencias Médicas, Escuela de Ciencias de la Actividad Física, el Deporte y La Salud, Universidad de Santiago de Chile (USACH), Santiago, Chile.
Martin GottelandDepartamento de Nutricion, Facultad de Medicina, Universidad de Chile, Independencia 1027, Santiago, Chile.
Fabien MagnePrograma de Microbiología y Micología, Instituto de Ciencias Biomédicas, Facultad de Medicina, Universidad de Chile, Santiago, Chile.
Rodrigo ValenzuelaDepartamento de Nutricion, Facultad de Medicina, Universidad de Chile, Independencia 1027, Santiago, Chile.
Diego F Garcia-DiazDepartamento de Nutricion, Facultad de Medicina, Universidad de Chile, Independencia 1027, Santiago, Chile. digarcia@uchile.cl.

Funding

Agencia Nacional de Investigación y Desarrollo 1171550
6 · The paper itself

Abstract

Obesity is characterized by a pathological increase in white adipose tissue (WAT). In addition to WAT, humans and animals have brown (BAT) and beige adipose tissue, specialized in thermogenesis. Increasing thermogenesis could help treat obesity. Polyphenols, such as those found in Calafate (Berberis microphylla), promote thermogenesis, but their effectiveness depends on gut microbiota (GM) composition. This study aimed to evaluate the impact of a Calafate extract on GM composition and thermogenic activity of brown and beige adipose tissue in mice fed a high-fat diet (HFD). Forty 8-week-old C57BL/6J mice were subdivided into 4 groups: control diet (C), control/Calafate diet (CC), high-fat diet (HF) and high-fat/Calafate diet (HFC). CC and HFC groups received daily 50 mg total polyphenols/kg body weight of Calafate extract in the drink for 4 months. Before euthanasia, mice underwent an energy expenditure (EE) measurement. RT-PCR was used to evaluate transcripts of thermogenic markers in ATs. Short-chain fatty acids (SCFAs) and GM composition were analyzed in cecal contents. Calafate extract administration reduced weight gain and increased EE, regardless of diet. It also enhanced the expression of thermogenic markers in BAT and inguinal WAT. While no significant changes in GM α-diversity were found, Calafate extract administration influenced GM composition. Additionally, correlations were observed between thermogenic markers and the abundance of specific gut bacteria. In conclusion, Calafate extract prevents excessive weight gain in HFD-fed male mice, potentially via a thermogenic transcriptional response associated with an enriched abundance of SCFA-producing bacteria.

Indexed as

Gastrointestinal MicrobiomeObesityPlant ExtractsPolyphenolsThermogenesisAdipose Tissue, BrownAdipose Tissue, WhiteAnimalsCecumDiet, High-FatEnergy MetabolismHomeostasisMaleMiceMice, Inbred C57BLPlant ExtractsPolyphenolsBrown adipose tissueBrowning adipose tissueCalafateGut microbiotaPolyphenolsThermogenesis

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Registered trials

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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.