Evidence map›Paper›PMID 40227203›Full record

ArticleAntioxidants (Basel, Switzerland)2025

Sustainable Utilization of Coffee Pulp, a By-Product of Coffee Production: Effects on Metabolic Syndrome in Fructose-Fed Rats.

Nelson Andrade, Ilda Rodrigues, Francisca Carmo, Gabriela Campanher, Isabella Bracchi, Joanne Lopes, Emília Patrício, João T Guimarães, Juliana A Barreto-Peixoto, Anabela S G Costa and 8 more

Abstract read
In one paragraph

Article in Antioxidants (Basel, Switzerland), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Article
  2. Article
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

18 authors.

Nelson AndradeLaboratório Associado para a Química Verde-Tecnologias e Processos Limpos (REQUIMTE/LAQV), Department of Chemical Sciences, Faculty of Pharmacy, University of Porto, 4050-313 Porto, Portugal.
Ilda RodriguesUnit of Biochemistry, Department of Biomedicine, Faculty of Medicine of Porto, University of Porto, 4200-465 Porto, Portugal.
Francisca CarmoUnit of Biochemistry, Department of Biomedicine, Faculty of Medicine of Porto, University of Porto, 4200-465 Porto, Portugal.
Gabriela CampanherUnit of Biochemistry, Department of Biomedicine, Faculty of Medicine of Porto, University of Porto, 4200-465 Porto, Portugal.
Isabella BracchiUnit of Biochemistry, Department of Biomedicine, Faculty of Medicine of Porto, University of Porto, 4200-465 Porto, Portugal.
Joanne LopesDepartment of Pathology, São João Hospital Centre, 4200-319 Porto, Portugal.
Emília PatrícioDepartment of Pathology, São João Hospital Centre, 4200-319 Porto, Portugal.ORCID 0000-0002-3045-5802
João T GuimarãesUnit of Biochemistry, Department of Biomedicine, Faculty of Medicine of Porto, University of Porto, 4200-465 Porto, Portugal.ORCID 0000-0003-4836-6311
Juliana A Barreto-PeixotoLaboratório Associado para a Química Verde-Tecnologias e Processos Limpos (REQUIMTE/LAQV), Department of Chemical Sciences, Faculty of Pharmacy, University of Porto, 4050-313 Porto, Portugal.ORCID 0000-0002-1853-1622
Anabela S G CostaLaboratório Associado para a Química Verde-Tecnologias e Processos Limpos (REQUIMTE/LAQV), Department of Chemical Sciences, Faculty of Pharmacy, University of Porto, 4050-313 Porto, Portugal.ORCID 0000-0003-4136-935X
Liliana Espírito SantoLaboratório Associado para a Química Verde-Tecnologias e Processos Limpos (REQUIMTE/LAQV), Department of Chemical Sciences, Faculty of Pharmacy, University of Porto, 4050-313 Porto, Portugal.
Marlene MachadoLaboratório Associado para a Química Verde-Tecnologias e Processos Limpos (REQUIMTE/LAQV), Department of Chemical Sciences, Faculty of Pharmacy, University of Porto, 4050-313 Porto, Portugal.
Thiago F SoaresLaboratório Associado para a Química Verde-Tecnologias e Processos Limpos (REQUIMTE/LAQV), Department of Chemical Sciences, Faculty of Pharmacy, University of Porto, 4050-313 Porto, Portugal.
Susana MachadoLaboratório Associado para a Química Verde-Tecnologias e Processos Limpos (REQUIMTE/LAQV), Department of Chemical Sciences, Faculty of Pharmacy, University of Porto, 4050-313 Porto, Portugal.ORCID 0000-0002-4567-0687
Maria Beatriz P P OliveiraLaboratório Associado para a Química Verde-Tecnologias e Processos Limpos (REQUIMTE/LAQV), Department of Chemical Sciences, Faculty of Pharmacy, University of Porto, 4050-313 Porto, Portugal.ORCID 0000-0002-6767-6596
Rita C AlvesLaboratório Associado para a Química Verde-Tecnologias e Processos Limpos (REQUIMTE/LAQV), Department of Chemical Sciences, Faculty of Pharmacy, University of Porto, 4050-313 Porto, Portugal.ORCID 0000-0002-5053-513X
Fátima MartelUnit of Biochemistry, Department of Biomedicine, Faculty of Medicine of Porto, University of Porto, 4200-465 Porto, Portugal.ORCID 0000-0002-0525-3416
Cláudia SilvaLaboratório Associado para a Química Verde-Tecnologias e Processos Limpos (REQUIMTE/LAQV), Department of Chemical Sciences, Faculty of Pharmacy, University of Porto, 4050-313 Porto, Portugal.ORCID 0000-0003-2937-974X

Funding

Fundação para a Ciência e Tecnologia PTDC/SAU-NUT/2165/2021
6 · The paper itself

Abstract

Metabolic syndrome (MetS) is a cluster of metabolic abnormalities that include insulin resistance, impaired glucose tolerance, dyslipidemia, hypertension, and abdominal obesity. Coffee production generates large quantities of waste products, which pose a serious threat to the environment. However, coffee by-products, such as coffee pulp (CP), possess an undeniable wealth of bioactive components. Based on this, we investigated whether a 10-week dietary intervention with 250 mg/kg/d of CP could prevent or ameliorate MetS in high-fructose-fed rats. Consumption of CP by rats fed a high-fructose diet reduced body weight gain, lowered systolic blood pressure (SBP), fasting plasma glucose and insulin levels, and improved insulin resistance compared to rats fed a high-fructose diet alone. At the hepatic level, CP attenuated the increase in lipid storage, reduced lipid peroxidation, and improved glutathione levels when combined with a high-fructose diet. CP also affected the expression of key genes related to glucose and lipid metabolism in hepatic and adipose tissues, in rats fed a fructose-rich diet. This study demonstrates that CP ameliorates several consequences of high-fructose-induced MetS in the rat (weight gain, hypertension, glucose intolerance, insulin resistance, changes in liver, and adipose tissue function). Hence, our data provide evidence that CP consumption in the context of a high-fructose diet can be used to improve MetS management.

Indexed as

adipose tissuecoffee pulpfructoselivermetabolic syndrome

Identifiers

PMID40227203
PMCPMC11939298

What OpenQuestion holds

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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.