Evidence map›Paper›PMID 36139762›Full record

ArticleAntioxidants (Basel, Switzerland)2022

Exercise Improves Redox Homeostasis and Mitochondrial Function in White Adipose Tissue.

Leonardo Matta, Caroline Coelho de Faria, Dahienne F De Oliveira, Iris Soares Andrade, Niedson Correia Lima-Junior, Bianca Martins Gregório, Cristina Maeda Takiya, Andrea Claudia Freitas Ferreira, José Hamilton M Nascimento, Denise Pires de Carvalho and 3 more

Open access · goldAbstract read
In one paragraph

Article in Antioxidants (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.2field-weighted citation impact, top 22% 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

8 citing papers in PubMed, 11 citations in OpenAlex.

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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

13 authors at 3 institutions in 2 countries.

Leonardo MattaHealth Science Center, Carlos Chagas Filho Institute of Biophysics, Federal University of Rio de Janeiro, 21941-590 Rio de Janeiro, Brazil.ORCID 0000-0002-3892-6330
Caroline Coelho de FariaHealth Science Center, Carlos Chagas Filho Institute of Biophysics, Federal University of Rio de Janeiro, 21941-590 Rio de Janeiro, Brazil.
Dahienne F De OliveiraHealth Science Center, Carlos Chagas Filho Institute of Biophysics, Federal University of Rio de Janeiro, 21941-590 Rio de Janeiro, Brazil.
Iris Soares AndradeHealth Science Center, Carlos Chagas Filho Institute of Biophysics, Federal University of Rio de Janeiro, 21941-590 Rio de Janeiro, Brazil.
Niedson Correia Lima-JuniorHealth Science Center, Carlos Chagas Filho Institute of Biophysics, Federal University of Rio de Janeiro, 21941-590 Rio de Janeiro, Brazil.
Bianca Martins GregórioUrogenital Research Unit, Roberto Alcântara Gomes Institute of Biology, State University of Rio de Janeiro, 20511-010 Rio de Janeiro, Brazil.
Cristina Maeda TakiyaHealth Science Center, Carlos Chagas Filho Institute of Biophysics, Federal University of Rio de Janeiro, 21941-590 Rio de Janeiro, Brazil.ORCID 0000-0002-8019-628X
Andrea Claudia Freitas FerreiraHealth Science Center, Carlos Chagas Filho Institute of Biophysics, Federal University of Rio de Janeiro, 21941-590 Rio de Janeiro, Brazil.ORCID 0000-0001-7300-2718
José Hamilton M NascimentoHealth Science Center, Carlos Chagas Filho Institute of Biophysics, Federal University of Rio de Janeiro, 21941-590 Rio de Janeiro, Brazil.ORCID 0000-0001-7052-254X
Denise Pires de CarvalhoHealth Science Center, Carlos Chagas Filho Institute of Biophysics, Federal University of Rio de Janeiro, 21941-590 Rio de Janeiro, Brazil.ORCID 0000-0001-6933-6424
Alexander BarteltInstitute for Cardiovascular Prevention, Klinikum der Universität München, Ludwig-Maximilians-University Munich, 80539 München, Germany.ORCID 0000-0001-7840-3991
Leonardo MacielHealth Science Center, Carlos Chagas Filho Institute of Biophysics, Federal University of Rio de Janeiro, 21941-590 Rio de Janeiro, Brazil.
Rodrigo Soares FortunatoHealth Science Center, Carlos Chagas Filho Institute of Biophysics, Federal University of Rio de Janeiro, 21941-590 Rio de Janeiro, Brazil.ORCID 0000-0003-3497-8173
Universidade Federal do Rio de Janeiro · BRLudwig-Maximilians-Universität München · DEUniversidade do Estado do Rio de Janeiro · BR

Funding

Coordenação de Aperfeicoamento de Pessoal de Nível Superior RFEuropean Research Council PROTEOFITFundação de Amparo à Pesquisa do Estado do Rio de Janeiro RFNational Council for Scientific and Technological Development RF
6 · The paper itself

Abstract

Exercise has beneficial effects on energy balance and also improves metabolic health independently of weight loss. Adipose tissue function is a critical denominator of a healthy metabolism but the adaptation of adipocytes in response to exercise is insufficiently well understood. We have previously shown that one aerobic exercise session was associated with increased expression of antioxidant and cytoprotective genes in white adipose tissue (WAT). In the present study, we evaluate the chronic effects of physical exercise on WAT redox homeostasis and mitochondrial function. Adult male Wistar rats were separated into two groups: a control group that did not exercise and a group that performed running exercise sessions on a treadmill for 30 min, 5 days per week for 9 weeks. Reactive oxygen species (ROS) generation, antioxidant enzyme activities, mitochondrial function, markers of oxidative stress and inflammation, and proteins related to DNA damage response were analyzed. In WAT from the exercise group, we found higher mitochondrial respiration in states I, II, and III of Complex I and Complex II, followed by an increase in ATP production, and the ROS/ATP ratio when compared to tissues from control rats. Regarding redox homeostasis, NADPH oxidase activity, protein carbonylation, and lipid peroxidation levels were lower in WAT from the exercise group when compared to control tissues. Moreover, antioxidant enzymatic activity, reduced glutathione/oxidized glutathione ratio, and total nuclear factor erythroid-2, like-2 (NFE2L2/NRF2) protein levels were higher in the exercise group compared to control. Finally, we found that exercise reduced the phosphorylation levels of H2AX histone (γH2AX), a central protein that contributes to genome stability through the signaling of DNA damage. In conclusion, our results show that chronic exercise modulates redox homeostasis in WAT, improving antioxidant capacity, and mitochondrial function. This hormetic remodeling of adipocyte redox balance points to improved adipocyte health and seems to be directly associated with the beneficial effects of exercise.

Indexed as

adipose tissueexercisehormesisredox homeostasis

Identifiers

PMID36139762
PMCPMC9495527
OpenAlexW4293527336

What OpenQuestion holds

Textmetadata
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.