Evidence map›Paper›PMID 40521450›Full record

ArticleACS omega2025

Pharmacological Potential of Cafestol, a Bioactive Substance in Coffee, in Preventing Ischemia-Reperfusion-Induced Acute Kidney Injury.

Dayene S Gomes, Mayara A Romanelli, Stela P S Gomes, Ana Laura M Brand, Rodrigo M V da Silva, Simone S C Oliveira, André L S Santos, Claudia M Rezende, Lucienne S Lara

Abstract read
In one paragraph

Article in ACS omega, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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

9 authors.

Dayene S GomesInstituto de Ciências Biomédicas, Universidade Federal do Rio de Janeiro, Rio de Janeiro, RJ 21941-902, Brazil.
Mayara A RomanelliInstituto de Ciências Biomédicas, Universidade Federal do Rio de Janeiro, Rio de Janeiro, RJ 21941-902, Brazil.
Stela P S GomesInstituto de Ciências Biomédicas, Universidade Federal do Rio de Janeiro, Rio de Janeiro, RJ 21941-902, Brazil.
Ana Laura M BrandInstituto de Química, Centro de Ciências Matemáticas e da Natureza, Universidade Federal do Rio de Janeiro, Rio de Janeiro, RJ 21941-909, Brazil.ORCID https://orcid.org/0009-0003-4963-6376
Rodrigo M V da SilvaInstituto de Química, Centro de Ciências Matemáticas e da Natureza, Universidade Federal do Rio de Janeiro, Rio de Janeiro, RJ 21941-909, Brazil.
Simone S C OliveiraInstituto de Microbiologia Paulo de Góes, Universidade Federal do Rio de Janeiro, Rio de Janeiro, RJ 21941-902, Brazil.
André L S SantosInstituto de Microbiologia Paulo de Góes, Universidade Federal do Rio de Janeiro, Rio de Janeiro, RJ 21941-902, Brazil.ORCID https://orcid.org/0000-0003-0821-8592
Claudia M RezendeInstituto de Química, Centro de Ciências Matemáticas e da Natureza, Universidade Federal do Rio de Janeiro, Rio de Janeiro, RJ 21941-909, Brazil.ORCID https://orcid.org/0000-0003-2710-5702
Lucienne S LaraInstituto de Ciências Biomédicas, Universidade Federal do Rio de Janeiro, Rio de Janeiro, RJ 21941-902, Brazil.ORCID https://orcid.org/0000-0002-2204-8799

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Renal ischemia-reperfusion (I/R) is the leading cause of acute kidney injury (AKI) and is a relevant complication of kidney transplantation. This work evaluated whether a single dose of cafestol (CAF) prevents I/R-induced AKI. We randomly divided male Wistar rats (180-220 g) into sham-operated groups (CTRL) or I/R surgery groups (I/R), which received either CAF 50 mg/kg or 75 mg/kg orally 2 h before the I/R procedure. During 24 h of reperfusion, rats were placed in metabolic cages for urine collection. The rats were euthanized, blood and urine were stored for renal function analyses, and the kidneys were collected for biochemical and histological studies. The I/R rats developed AKI, as evidenced by kidney damage (space between tubules, glomerular segmentation, and marked collagen accumulation throughout the renal tissue) and a decline in function and Na

Identifiers

PMID40521450
PMCPMC12163779

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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.