Evidence map›Paper›PMID 26081690›Full record

ArticleJournal of cellular and molecular medicine2015

Melatonin protects ADSCs from ROS and enhances their therapeutic potency in a rat model of myocardial infarction.

Ping Zhu, Jianfeng Liu, Jinxin Shi, Qian Zhou, Jie Liu, Xianwei Zhang, Zhiyan Du, Qiaowei Liu, Yuanyuan Guo

Open access · goldAbstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed, 1 pooled it
8.3field-weighted citation impact, top 2% 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

44 citing papers in PubMed, 1 synthesis or guideline pooled it, 81 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Melatonin and angiogenesis potential in stem cells.Stem cell research & therapy · 2025
    Review
  4. Review
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  8. Article
  9. Article
  10. Article
  11. Melatonin and the Programming of Stem Cells.International journal of molecular sciences · 2022
    Review
  12. Evidence for the Benefits of Melatonin in Cardiovascular Disease.Frontiers in cardiovascular medicine · 2022
    Review
  13. Article
  14. Article
  15. Review
  16. Review
  17. Review
  18. Article
  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 at 6 institutions in 1 country.

Ping ZhuDepartment of Geriatric Cardiology, Chinese PLA General Hospital, Beijing, China.
Jianfeng LiuDepartment of Geriatric Cardiology, Chinese PLA General Hospital, Beijing, China.
Jinxin ShiShijingshan Teaching Hospital of Capital Medical University, Beijing Shijingshan Hospital, Beijing, China.
Qian ZhouDepartment of Cardiology, The Center Hospital of Zhoukou, Henan Province, China.
Jie LiuDepartment of Geriatric Cardiology, Chinese PLA General Hospital, Beijing, China.
Xianwei ZhangThe Health Department of Guard Bureau in the General Staff, Beijing, China.
Zhiyan DuInstitute of Basic Medical Sciences, Academy of Military Medical Sciences, Beijing, China.
Qiaowei LiuBeijing Institute of Radiation Medicine, Beijing, China.
Yuanyuan GuoShijingshan Teaching Hospital of Capital Medical University, Beijing Shijingshan Hospital, Beijing, China.
Chinese PLA General Hospital · CNAcademy of Military Medical Sciences · CNBeijing Radiation Center · CNBeijing Shijingshan Hospital · CNCapital Medical University · CNZhoukou City Academy of Agricultural Sciences · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Myocardial infarction (MI) is a major cause of death and disability worldwide. In the last decade, mesenchymal stem cells (MSCs) based cell therapy has emerged as a promising therapeutic strategy. Although great advance have been made using MSCs to treat MI, the low viability of transplanted MSCs severely limits the efficiency of MSCs therapy. Here, we show evidence that ex vivo pre-treatment with melatonin, an endogenous hormone with newly found anti-oxidative activity, could improve survival and function of adipose tissue derived MSCs (ADSCs) in vitro as well as in vivo. ADSCs with 5 μM melatonin pre-treatment for 24 hrs showed increased expression of the antioxidant enzyme catalase and Cu/Zn superoxide dismutase (SOD-1), as well as pro-angiogenic and mitogenic factors like insulin-like growth factor 1, basic fibroblast growth factor, hepatocyte growth factor (HGF), epidermal growth factor. Furthermore, melatonin pre-treatment protected MSCs from reactive oxygen species (ROS) induced apoptosis both directly by promoting anti-apoptosis kinases like p-Akt as well as blocking caspase cascade, and indirectly by restoring the ROS impaired cell adhesion. Using a rat model of MI, we found that melatonin pre-treatment enhanced the viability of engrafted ADSCs, and promoted their therapeutic potency. Hopefully, our results may shed light on the design of more effective therapeutic strategies treating MI by MSCs in clinic.

Indexed as

Stem Cell TransplantationAdipose TissueAngiogenesis Inducing AgentsAnimalsAntioxidantsApoptosisCells, CulturedCell SurvivalCytoprotectionDisease Models, AnimalFlow CytometryHeart VentriclesMaleMelatoninMitogensMyocardial InfarctionAngiogenesis Inducing AgentsAntioxidantsMelatoninMitogensReactive Oxygen Speciesadipose tissue derived MSCsapoptosismelatoninmyocardial infarctionrat modelreactive oxygen speciestherapeutic strategyviability

Identifiers

PMID26081690
PMCPMC4568927
OpenAlexW1566998770

What OpenQuestion 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 OpenQuestion graph.