Evidence map›Paper›PMID 33504680›Full record

ArticleThe Journal of endocrinology2021

Apelin/APJ relieve diabetic cardiomyopathy by reducing microvascular dysfunction.

Bin Li, Jiming Yin, Jing Chang, Jia Zhang, Yangjia Wang, Haixia Huang, Wei Wang, Xiangjun Zeng

Open access · hybridAbstract read
In one paragraph

Article in The Journal of endocrinology, 2021. 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
2.9field-weighted citation impact, top 9% 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

21 citing papers in PubMed, 29 citations in OpenAlex.

  1. miR‑222‑3p inhibits diabetic skin wound healing by targeting APLN.International journal of molecular medicine · 2026
    Article
  2. Review
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  8. Article
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  12. Review
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  14. Preeclampsia and Obesity-The Preventive Role of Exercise.International journal of environmental research and public health · 2023
    Review
  15. Endothelial cell dysfunction in cardiac disease: driver or consequence?Frontiers in cell and developmental biology · 2023
    Review
  16. Article
  17. Review
  18. The Protective Role of Apelin in the Early Stages of Diabetic Retinopathy.International journal of molecular sciences · 2022
    Article
  19. Research progress of apelin in acute ischemic brain injury.American journal of translational research · 2022
    Review
  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

8 authors at 2 institutions in 1 country.

Bin LiSchool of Basic Medical Sciences, Capital Medical University, Beijing, China.
Jiming YinBeijing You An Hospital, Capital Medical University, Beijing, China.
Jing ChangBeijing You An Hospital, Capital Medical University, Beijing, China.
Jia ZhangSchool of Basic Medical Sciences, Capital Medical University, Beijing, China.
Yangjia WangSchool of Basic Medical Sciences, Capital Medical University, Beijing, China.
Haixia HuangSchool of Basic Medical Sciences, Capital Medical University, Beijing, China.
Wei WangSchool of Basic Medical Sciences, Capital Medical University, Beijing, China.
Xiangjun ZengSchool of Basic Medical Sciences, Capital Medical University, Beijing, China.ORCID 0000-0002-2553-2244
Capital Medical University · CNBeijing YouAn Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Microcirculatory injuries had been reported to be involved in diabetic cardiomyopathy, which was mainly related to endothelial cell dysfunction. Apelin, an adipokine that is upregulated in diabetes mellitus, was reported to improve endothelial cell dysfunction and attenuate cardiac insufficiency induced by ischemia and reperfusion. Therefore, it is hypothesized that apelin might be involved in alleviating endothelial cell dysfunction and followed cardiomyopathy in diabetes mellitus. The results showed that apelin improved endothelial cell dysfunction via decreasing apoptosis and expression of adhesion molecules and increasing proliferation, angiogenesis, and expression of E-cadherin, VEGFR 2 and Tie-2 in endothelial cells, which resulted in the attenuation of the capillary permeability in cardiac tissues and following diabetic cardiomyopathy. Meanwhile, the results from endothelial cell-specific APJ knockout mice and cultured endothelial cells confirmed that the effects of apelin on endothelial cells were dependent on APJ and the downstream NFκB pathways. In conclusion, apelin might reduce microvascular dysfunction induced by diabetes mellitus via improving endothelial dysfunction dependent on APJ activated NFκB pathways.

Indexed as

AnimalsApelinApelin ReceptorsBlood GlucoseCell Adhesion MoleculesCells, CulturedDiabetes Mellitus, ExperimentalDiabetes Mellitus, Type 2Diabetic CardiomyopathiesEndothelial CellsInflammationMaleMiceMice, Inbred C57BLMice, KnockoutMicrovesselsApelinApelin ReceptorsAplnr protein, mouseBlood GlucoseCell Adhesion MoleculesNF-kappa BapelinAPJdiabetic cardiomyopathyendothelial dysfunctionmicrocirculatory injuries

Identifiers

PMID33504680
PMCPMC8052525
OpenAlexW3198112489

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.