Evidence map›Paper›PMID 23624753›Full record

ArticleNaunyn-Schmiedeberg's archives of pharmacology2013

Vitexin protects against cardiac hypertrophy via inhibiting calcineurin and CaMKII signaling pathways.

Cui-cui Lu, Ying-qi Xu, Ji-chao Wu, Peng-zhou Hang, Yan Wang, Chen Wang, Jian-wei Wu, Jian-cui Qi, Yong Zhang, Zhi-min Du

Abstract read
PubMed Publisher
In one paragraph

Article in Naunyn-Schmiedeberg's archives of pharmacology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.8field-weighted citation impact, top 16% 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

15 citing papers in PubMed, 43 citations in OpenAlex.

  1. Beneficial Role of Vitexin in Parkinson's Disease.The Malaysian journal of medical sciences : MJMS · 2023
    Review
  2. The Aerial Parts ofMolecules (Basel, Switzerland) · 2021
    Article
  3. Vitexin inhibits APEX1 to counteract the flow-induced endothelial inflammation.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  4. Review
  5. Natural Products as Modulators of Sirtuins.Molecules (Basel, Switzerland) · 2020
    Review
  6. Review
  7. Heliyon · 2019
    Article
  8. Protective effects of five compounds fromDrug design, development and therapy · 2019
    Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Cardioprotective Effects ofJournal of evidence-based integrative medicine
    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

10 authors at 2 institutions in 1 country.

Cui-cui LuInstitute of Clinical Pharmacology, The Second Affiliated Hospital, Harbin Medical University, Harbin, 150086, Heilongjiang, People's Republic of China.
Ying-qi Xu
Ji-chao Wu
Peng-zhou Hang
Yan Wang
Chen Wang
Jian-wei Wu
Jian-cui Qi
Yong Zhang
Zhi-min Du
Harbin Medical University · CNSecond Affiliated Hospital of Harbin Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Vitexin is a flavone glycoside isolated from the leaf of Crataeguspinnatifida Bunge, the utility of which has been demonstrated in several cardiovascular diseases. However, its role in cardiac hypertrophy remains unclear. In the present study, we aimed to determine whether vitexin prevents cardiac hypertrophy induced by isoproterenol (ISO) in cultured neonatal rat ventricular myocytes in vitro and pressure overload-induced cardiac hypertrophy in mice in vivo. The results revealed that vitexin (10, 30, and 100 μM) dose-dependently attenuated cardiac hypertrophy induced by ISO in vitro. Furthermore, vitexin (3, 10, and 30 mg kg(-1)) prevented cardiac hypertrophy induced by transverse aortic constriction as assessed by heart weight/body weight, left ventricular weight/body weight and lung weight/body weight ratios, cardiomyocyte cross-sectional area, echocardiographic parameters, and gene expression of hypertrophic markers. Further investigation demonstrated that vitexin inhibited the increment of the resting intracellular free calcium induced by ISO. Vitexin also inhibited the expression of calcium downstream effectors calcineurin-NFATc3 and phosphorylated calmodulin kinase II (CaMKII) both in vitro and in vivo. Taken together, our results indicate that vitexin has the potential to protect against cardiac hypertrophy through Ca2+-mediated calcineurin-NFATc3 and CaMKII signaling pathways.

Indexed as

Calcineurin InhibitorsAnimalsAnimals, NewbornApigeninCalcineurinCalcium-Calmodulin-Dependent Protein Kinase Type 2CardiomegalyCardiotonic AgentsCells, CulturedIsoproterenolMaleMiceMyocytes, CardiacPressureRatsRats, WistarApigeninCalcineurinCalcineurin InhibitorsCalcium-Calmodulin-Dependent Protein Kinase Type 2Cardiotonic AgentsIsoproterenolvitexin

Identifiers

PMID23624753
OpenAlexW1976674477

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.