Evidence map›Paper›PMID 32274619›Full record

ArticleCardiovascular toxicology2020

TRPV4 Mediates Cardiac Fibrosis via the TGF-β1/Smad3 Signaling Pathway in Diabetic Rats.

Xiaoli Jia, Chao Xiao, Deqiao Sheng, Mengcheng Yang, Quanyi Cheng, Jing Wu, Shizhong Zhang

Abstract read
PubMed Publisher
In one paragraph

Article in Cardiovascular toxicology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.9field-weighted citation impact, top 12% 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

18 citing papers in PubMed, 21 citations in OpenAlex.

  1. Review
  2. Review
  3. TRPV4-Mediated Mechanosensing Regulates the Endothelial-to-Mesenchymal Transition: Implications for Atherosclerosis.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2025
    Article
  4. Review
  5. Review
  6. Article
  7. CaBiomedicines · 2025
    Review
  8. Review
  9. Review
  10. Article
  11. Review
  12. Hydrogel cultures reveal Transient Receptor Potential Vanilloid 4 regulation of myofibroblast activation and proliferation in valvular interstitial cells.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2022
    Article
  13. Review
  14. Review
  15. Review
  16. Article
  17. Review
  18. 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

7 authors at 1 institution in 1 country.

Xiaoli Jia *Department of Physiology, Medical College of China Three Gorges University, 8 Daxue Road, Yichang, 443002, Hubei, China.
Chao Xiao *Department of Physiology, Medical College of China Three Gorges University, 8 Daxue Road, Yichang, 443002, Hubei, China.
Deqiao ShengDepartment of Physiology, Medical College of China Three Gorges University, 8 Daxue Road, Yichang, 443002, Hubei, China.
Mengcheng YangDepartment of Physiology, Medical College of China Three Gorges University, 8 Daxue Road, Yichang, 443002, Hubei, China.
Quanyi ChengDepartment of Physiology, Medical College of China Three Gorges University, 8 Daxue Road, Yichang, 443002, Hubei, China.
Jing WuDepartment of Physiology, Medical College of China Three Gorges University, 8 Daxue Road, Yichang, 443002, Hubei, China.
Shizhong ZhangDepartment of Physiology, Medical College of China Three Gorges University, 8 Daxue Road, Yichang, 443002, Hubei, China. zhangsz@ctgu.edu.cn.
China Three Gorges University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Emerging evidence shows that the transient receptor potential vanilloid 4 (TRPV4) channel is involved in fibrosis in many organs. However, its role in diabetic cardiac fibrosis remains unclear. Our aim was to evaluate the expression level of TRPV4 in the diabetic heart and clarify its role in diabetes-induced cardiac fibrosis. A diabetic animal model was induced by a single intraperitoneal injection of streptozotocin into Sprague-Dawley rats. We also investigated cardiac fibroblasts isolated from neonatal Sprague-Dawley rats. TRPV4 expression was significantly upregulated in both diabetic myocardium and cardiac fibroblasts cultured in high-glucose medium. Masson's trichrome staining revealed that the TRPV4 antagonist HC067047 attenuated the diabetes-induced cardiac fibrosis. Furthermore, HC067047 reduced collagen Ι synthesis and suppressed the transforming growth factor beta 1 (TGF-β1) level as well as the phosphorylation of Smad3 in the diabetic heart. In addition, the TRPV4 antagonist inhibited the proliferation of cardiac fibroblasts, collagen Ι synthesis, and activation of the TGF-β1/Smad3 signaling pathway induced by high-glucose culture medium. Our findings demonstrate that the upregulation of TRPV4 expression mediates diabetic cardiac fibrosis via activation of the TGF-β1/Smad3 signaling pathway.

Indexed as

AnimalsCell ProliferationCells, CulturedCollagen Type IDiabetes Mellitus, ExperimentalDiabetic CardiomyopathiesFibroblastsFibrosisMaleMorpholinesMyocardiumPhosphorylationPyrrolesRats, Sprague-DawleySignal TransductionSmad3 ProteinCollagen Type IHC-067047MorpholinesPyrrolesSmad3 ProteinSmad3 protein, ratTgfb1 protein, ratTransforming Growth Factor beta1Trpv4 protein, ratTRPV Cation ChannelsDiabetes mellitusFibroblastsMyocardiumTRPV4 channel

Identifiers

PMID32274619
OpenAlexW3015433413

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.