Evidence map›Paper›PMID 30513114›Full record

ArticlePloS one2018

Effects of acute hypoxia exposure with different durations on activation of Nrf2-ARE pathway in mouse skeletal muscle.

Weixiu Ji, Linjia Wang, Shiyi He, Lu Yan, Tieying Li, Jianxiong Wang, Ah-Ng Tony Kong, Siwang Yu, Ying Zhang

Abstract read
In one paragraph

Article in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing 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

20 citing papers in PubMed.

  1. Article
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  10. Article
  11. Article
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  14. Potential Role of APEX1 During Ferroptosis.Frontiers in oncology · 2022
    Review
  15. Article
  16. Article
  17. Muscle-derived exosomes encapsulate myomiRs and are involved in local skeletal muscle tissue communication.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2021
    Article
  18. Article
  19. Article
  20. Regulation of Gene Expression under Hypoxic Conditions.International journal of molecular sciences · 2019
    Review
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.

Weixiu JiSchool of Sport Science, Beijing Sport University, Beijing, China.
Linjia WangSchool of Sport Science, Beijing Sport University, Beijing, China.
Shiyi HeSchool of Sport Science, Beijing Sport University, Beijing, China.
Lu YanSchool of Sport Science, Beijing Sport University, Beijing, China.
Tieying LiSchool of Sport Science, Beijing Sport University, Beijing, China.
Jianxiong WangFaculty of Health, Engineering, and Sciences, University of Southern Queensland, Toowoomba, Queensland, Australia.
Ah-Ng Tony KongErnest Mario School of Pharmacy, Rutgers, the State University of New Jersey, Camden, New Jersey, United States of America.
Siwang YuDepartment of Chemical Biology, School of Pharmaceutical Sciences, Peking University, Beijing, China.
Ying ZhangSchool of Sport Science, Beijing Sport University, Beijing, China.ORCID 0000-0002-2248-3678

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHypoxia training enhances the endurance capacity of athletes. This response may in part be attributed to the hypoxia-induced increase in antioxidant capacity in skeletal muscles. Nuclear factor erythroid 2-related factor 2 (Nrf2), a key transcription factor which regulates the expression of genes via binding to the antioxidant-response element (ARE) of these genes, plays a crucial role in stimulating the body's defense system and potentially responds to hypoxia. Meanwhile, hypoxia-inducible factor-1α (HIF-1α) is an important player in protecting cells from hypoxic stress. The purpose of this study was to investigate the effects of acute hypoxia exposure with different durations on the activation of Nrf2-ARE pathway and a possible regulatory role of HIF-1α in these responses.

methodsC57BL/6J mice were allocated into the non-hypoxia 0-hour, 6-hour, 24-hour, and 48-hour hypoxic exposure (11.2% oxygen) groups. The quadriceps femoris was collected immediately after hypoxia. Further, to investigate the possible role of HIF-1α, C2C12 myoblasts with HIF-1α knockdown by small interfering RNA (siRNA) and the inducible HIF-1α transgenic mice were employed.

resultsThe results showed that 48-hour hypoxia exposure up-regulated protein expression of Nrf2, Nrf2/ARE binding activity and the transcription of antioxidative genes containing ARE (Sod1 and others) in mouse skeletal muscle. Moreover, HIF-1α siRNA group of C2C12 myoblasts showed a remarkable inhibition of Nrf2 protein expression and nuclear accumulation in hypoxia exposure for 72 hours compared with that in siRNA-Control group of the cells. In addition, HIF-1α transgenic mice gave higher Nrf2 protein expression, Nrf2/ARE binding activity and expressions of Nrf2-mediated antioxidative genes in their skeletal muscle, compared with those in the wild-type mice.

conclusionsThe findings suggested that the acute hypoxia exposure could trigger the activation of Nrf2-ARE pathway, with longer duration associated with higher responses, and HIF-1α expression might be involved in promoting the Nrf2-mediated antioxidant responses in skeletal muscle.

Indexed as

HypoxiaAnimalsAntioxidant Response ElementsAntioxidantsCell HypoxiaCells, CulturedFemaleGene Expression RegulationHypoxia-Inducible Factor 1, alpha SubunitMaleMiceMice, Inbred C57BLMice, TransgenicMuscle, SkeletalNF-E2-Related Factor 2OxygenAntioxidantsHif1a protein, mouseHypoxia-Inducible Factor 1, alpha SubunitNF-E2-Related Factor 2Oxygen

Identifiers

PMID30513114
PMCPMC6279028

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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.