Evidence map›Paper›PMID 33780353›Full record

ArticleAging2021

Chronic treatment with acetaminophen protects against liver aging by targeting inflammation and oxidative stress.

Rocío Brea, Pilar Valdecantos, Patricia Rada, Rosa Alen, Carmelo García-Monzón, Lisardo Boscá, Marina Fuertes-Agudo, Marta Casado, Paloma Martín-Sanz, Ángela M Valverde

Open access · greenAbstract read
In one paragraph

Article in Aging, 2021. 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
0.2field-weighted citation impact, top 50% 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

2 citing papers in PubMed, 4 citations in OpenAlex.

  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

10 authors at 6 institutions in 1 country.

Rocío BreaInstituto de Investigaciones Biomédicas "Alberto Sols", (CSIC-UAM), Department of Metabolism and Cellular Signaling, Madrid 28029, Spain.
Pilar ValdecantosInstituto de Investigaciones Biomédicas "Alberto Sols", (CSIC-UAM), Department of Metabolism and Cellular Signaling, Madrid 28029, Spain.
Patricia RadaInstituto de Investigaciones Biomédicas "Alberto Sols", (CSIC-UAM), Department of Metabolism and Cellular Signaling, Madrid 28029, Spain.
Rosa AlenInstituto de Investigaciones Biomédicas "Alberto Sols", (CSIC-UAM), Department of Metabolism and Cellular Signaling, Madrid 28029, Spain.
Carmelo García-MonzónLiver Research Unit, Hospital Universitario Santa Cristina, Instituto de Investigación Sanitaria Princesa, Madrid 28009, Spain.
Lisardo BoscáInstituto de Investigaciones Biomédicas "Alberto Sols", (CSIC-UAM), Department of Metabolism and Cellular Signaling, Madrid 28029, Spain.
Marina Fuertes-AgudoInstituto de Biomedicina de Valencia (IBV-CSIC), Valencia 46010, Spain.
Marta CasadoInstituto de Biomedicina de Valencia (IBV-CSIC), Valencia 46010, Spain.
Paloma Martín-SanzInstituto de Investigaciones Biomédicas "Alberto Sols", (CSIC-UAM), Department of Metabolism and Cellular Signaling, Madrid 28029, Spain.
Ángela M ValverdeInstituto de Investigaciones Biomédicas "Alberto Sols", (CSIC-UAM), Department of Metabolism and Cellular Signaling, Madrid 28029, Spain.
Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas · ESCentro de Investigación Biomédica en Red Diabetes y Enfermedades Metabólicas Asociadas · ESInstituto de Salud Carlos III · ESUniversidad Autónoma de Madrid · ESCentro de Investigación Biomédica en Red · ESInstituto de Investigaciones Biomédicas Sols-Morreale · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The liver exhibits a variety of functions that are well-preserved during aging. However, the cellular hallmarks of aging increase the risk of hepatic alterations and development of chronic liver diseases. Acetaminophen (APAP) is a first choice for relieving mild-to-moderate pain. Most of the knowledge about APAP-mediated hepatotoxicity arises from acute overdose studies due to massive oxidative stress and inflammation, but little is known about its effect in age-related liver inflammation after chronic exposure. Our results show that chronic treatment of wild-type mice on the B6D2JRcc/Hsd genetic background with APAP at an infratherapeutic dose reduces liver alterations during aging without affecting body weight. This intervention attenuates age-induced mild oxidative stress by increasing HO-1, MnSOD and NQO1 protein levels and reducing ERK1/2 and p38 MAPK phosphorylation. More importantly, APAP treatment counteracts the increase in Cd8

Indexed as

AcetaminophenAgingAlanine TransaminaseAnimalsAspartate AminotransferasesInflammationLipid PeroxidationLiverL-Lactate DehydrogenaseMaleMiceOxidative StressProtective AgentsAcetaminophenAlanine TransaminaseAspartate AminotransferasesL-Lactate DehydrogenaseProtective AgentsagingAPAPinflammationliveroxidative stress

Identifiers

PMID33780353
PMCPMC8034963
OpenAlexW3143475922

What Socratic holds

Textmetadata
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 Socratic graph.