Evidence map›Paper›PMID 28260802›Full record

ArticleActa pharmacologica Sinica2017

Autophagy inhibitor 3-methyladenine alleviates overload-exercise-induced cardiac injury in rats.

Hua Liu, Hui Lei, Yue Shi, Jin-Ju Wang, Ning Chen, Zhang-Hua Li, Yan-Fang Chen, Qi-Fa Ye, Yi Yang

Abstract read
In one paragraph

Article in Acta pharmacologica Sinica, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing 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

21 citing papers in PubMed.

  1. Article
  2. Article
  3. [3-Methyladenine alleviates early renal injury in diabetic mice by inhibiting AKT signaling].Nan fang yi ke da xue xue bao = Journal of Southern Medical University · 2024
    Article
  4. Review
  5. Review
  6. Exercise sustains the hallmarks of health.Journal of sport and health science · 2023
    Review
  7. Article
  8. Article
  9. Role of adiponectin in osteoarthritis.Frontiers in cell and developmental biology · 2022
    Review
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. 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.

Hua LiuCollege of Health Science, Wuhan Sports University, Wuhan 430079, China.
Hui LeiCollege of Health Science, Wuhan Sports University, Wuhan 430079, China.
Yue ShiCollege of Health Science, Shanghai University of Sport, Shanghai 200438, China.
Jin-Ju WangDepartment of Pharmacology &Toxicology, Boonshoft School of Medicine, Wright State University, Dayton, OH 45435, USA.
Ning ChenCollege of Health Science, Wuhan Sports University, Wuhan 430079, China.
Zhang-Hua LiTongren Hospital of Wuhan University, Wuhan 430060, China.
Yan-Fang ChenDepartment of Pharmacology &Toxicology, Boonshoft School of Medicine, Wright State University, Dayton, OH 45435, USA.
Qi-Fa YeHepatobiliary Disease Institute of Wuhan University, Transplant Center of Wuhan University, Zhongnan Hospital of Wuhan University, Wuhan 430030, China.
Yi YangCollege of Health Science, Wuhan Sports University, Wuhan 430079, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Overload-exercise (OE) causes myocardial injury through inducing autophagy and apoptosis. In this study we examined whether an autophagy inhibitor 3-methyladenine (3-MA) could alleviate OE-induced cardiac injury. Rats were injected with 3-MA (15 mg/kg, iv) or saline before subjected to various intensities of OE, including no swim (control), 2 h swim (mild-intensity exercise, MIE), 2 h swim with 2.5% body weight overload (moderate OE; MOE), 5% overload (intensive OE; IOE) or 2.5% overload until exhausted (exhaustive OE; EOE). After OE, the hearts were harvested for morphological and biochemiacal analysis. The cardiac morphology, autophagosomes and apoptosis were examined with H&E staining, transmission electron microscopy and TUNEL analysis, respectively. Autophagy-related proteins to (LC3-II/I and Beclin-1) and apoptosis-related proteins (Bcl-2/Bax) were assessed using Western blotting. Our results showed that compared with the control, MIE did not change the morphological structures of the heart tissues that exhibited intact myocardial fibers and neatly arranged cardiomyocytes. However, IOE resulted in irregular arrangement of cardiomyocytes and significantly increased width of cardiomyocytes, whereas EOE caused more swollen and even disrupted cardiomyocytes. In parallel with the increased OE intensity (MOE, IOE, EOE), cardiomyocyte autophagy and apoptosis became more and more prominent, evidenced by the increasing number of autophagosomes and expression levels of LC3-II/I and Beclin-1 as well as the increasing apoptotic cells and decreasing Bcl-2/Bax ratio. 3-MA administration significantly attenuated OE-induced morphological changes of cardiomyocytes as well as all the autophagy- and apoptosis-related abnormalities in MOE, IOE and EOE rats. Thus, the autophagy inhibitor 3-MA could alleviate OE-induced heart injury in rats.

Indexed as

Physical Conditioning, AnimalAdenineAnimalsAutophagyDisease Models, AnimalHeart InjuriesMaleRatsRats, Sprague-Dawley3-methyladenineAdenine

Identifiers

PMID28260802
PMCPMC5519243

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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.