Evidence map›Paper›PMID 36650315›Full record

ArticleEuropean journal of nutrition2023

Astaxanthin promotes mitochondrial biogenesis and antioxidant capacity in chronic high-intensity interval training.

Yang Wang, Xiaoping Chen, Julien S Baker, Gareth W Davison, Shujun Xu, Yingsong Zhou, Xiaoming Bao

Open access · greenAbstract read
PubMed Publisher
In one paragraph

Article in European journal of nutrition, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
4.7field-weighted citation impact, top 5% 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

27 citing papers in PubMed, 34 citations in OpenAlex.

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  18. Frontiers in nutrition · 2025
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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

7 authors at 4 institutions in 3 countries.

Yang WangFaculty of Sports Science, Ningbo University, Ningbo, Zhejiang, People's Republic of China.
Xiaoping ChenFaculty of Sports Science, Ningbo University, Ningbo, Zhejiang, People's Republic of China.
Julien S BakerCentre for Health and Exercise Science Research, Hong Kong Baptist University, Kowloon Tong, 999077, HK, People's Republic of China.
Gareth W DavisonSport and Exercise Sciences Research Institute, Ulster University, Newtownabbey, BT37 0QB, UK.
Shujun XuSchool of Medicine, Ningbo University, Ningbo, Zhejiang, People's Republic of China.
Yingsong ZhouFaculty of Sports Science, Ningbo University, Ningbo, Zhejiang, People's Republic of China. zhouyingsong@nbu.edu.cn.ORCID http://orcid.org/0000-0002-9758-3673
Xiaoming BaoDepartment of Cardiology, Ningbo No.2 Hospital, Ningbo, Zhejiang, People's Republic of China. 18668271580@163.com.
Ningbo University · CNHong Kong Baptist University · HKNingbo No. 2 Hospital · CNUniversity of Ulster · GB

Funding

Natural Science Foundation of Ningbo 2019A610347
6 · The paper itself

Abstract

purposeReactive oxygen and nitrogen species are required for exercise-induced molecular adaptations; however, excessive exercise may cause cellular oxidative distress. We postulate that astaxanthin (ASX) can neutralize oxidative distress and stimulate mitochondrial biogenesis in high-intensity exercise-trained mice.

methodsSix-week-old mice (n = 8/group) were treated with ASX (10 mg/kg BW) or placebo. Training groups participated in 30 min/day high-intensity interval training (HIIT) for 6 weeks. Gastrocnemius muscle was collected and assayed following the exercise training period.

resultsCompared to the HIIT control mice, the ASX-treated HIIT mice reduced malonaldehyde levels and upregulated the expression of Nrf2 and FOXO3a. Meanwhile, the genes NQO1 and GCLC, modulated by Nrf2, and SOD2, regulated by FOXO3a, and GPx4, were transcriptionally upregulated in the ASX-treated HIIT group. Meanwhile, the expression of energy sensors, AMPK, SIRT1, and SIRT3, increased in the ASX-treated HIIT group compared to the HIIT control group. Additionally, PGC-1α, regulated by AMPK and SIRT1, was upregulated in the ASX-treated HIIT group. Further, the increased PGC-1α stimulated the transcript of NRF1 and Tfam and mitochondrial proteins IDH2 and ATP50. Finally, the ASX-treated HIIT mice had upregulations in the transcript level of mitochondrial fusion factors, including Mfn1, Mfn2, and OPA1. However, the protein level of AMPK, SIRT1, and FOXO3a, and the transcript level of Nrf2, NQO1, PGC-1α, NRF1, Mfn1, Mfn2, and OPA1 decreased in the HIIT control group compared to the sedentary control group.

conclusionSupplementation with ASX can reduce oxidative stress and promote antioxidant capacity and mitochondrial biogenesis during strenuous HIIT exercise in mice.

Indexed as

AntioxidantsHigh-Intensity Interval TrainingAMP-Activated Protein KinasesAnimalsMiceMuscle, SkeletalNF-E2-Related Factor 2Organelle BiogenesisPeroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alphaSirtuin 1XanthophyllsAMP-Activated Protein KinasesAntioxidantsastaxanthineNF-E2-Related Factor 2Peroxisome Proliferator-Activated Receptor Gamma Coactivator 1-alphaSirtuin 1XanthophyllsAstaxanthinHigh-intensity interval trainingMitochondrial biogenesisNrf2Oxidative stressPGC-1αRONS

Identifiers

PMID36650315
OpenAlexW4316927286

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.