Evidence map›Paper›PMID 25416190›Full record

ReviewAmerican journal of physiology. Heart and circulatory physiology2015

Role of TRP channels in the cardiovascular system.

Zhichao Yue, Jia Xie, Albert S Yu, Jonathan Stock, Jianyang Du, Lixia Yue

Open access · greenAbstract readReview
In one paragraph

Review in American journal of physiology. Heart and circulatory physiology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 101 papers.

0numbers the graph read from it
0cells of the map it votes in
101citing papers in PubMed
6.8field-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

101 citing papers in PubMed, 182 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. TRPM6 in murine kidneys-of targets and antibodies.Naunyn-Schmiedeberg's archives of pharmacology · 2025
    Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Review
  15. Impact of aging on vascular ion channels: perspectives and knowledge gaps across major organ systems.American journal of physiology. Heart and circulatory physiology · 2023
    Review
  16. The Dysfunction of CaInternational journal of molecular sciences · 2023
    Review
  17. Review
  18. Article
  19. Review
  20. Review

41 more citing papers are in PubMed but not listed here.

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

6 authors at 1 institution in 1 country.

Zhichao YueCalhoun Cardiology Center, Department of Cell Biology, University of Connecticut Health Center, Farmington, Connecticut.
Jia XieCalhoun Cardiology Center, Department of Cell Biology, University of Connecticut Health Center, Farmington, Connecticut.
Albert S YuCalhoun Cardiology Center, Department of Cell Biology, University of Connecticut Health Center, Farmington, Connecticut.
Jonathan StockCalhoun Cardiology Center, Department of Cell Biology, University of Connecticut Health Center, Farmington, Connecticut.
Jianyang DuCalhoun Cardiology Center, Department of Cell Biology, University of Connecticut Health Center, Farmington, Connecticut.
Lixia YueCalhoun Cardiology Center, Department of Cell Biology, University of Connecticut Health Center, Farmington, Connecticut lyue@uchc.edu.
UConn Health · US

Funding

Ca2+ signaling mechanisms in cardiac fibrosisR01HL078960 · NHLBI · UNIVERSITY OF CONNECTICUT SCH OF MED/DNT · PI YUE, LIXIA · 2005 to 2015
$3.9M
NHLBI NIH HHS 2R01 HL078960NHLBI NIH HHS R01 HL078960
6 · The paper itself

Abstract

The transient receptor potential (TRP) superfamily consists of a large number of nonselective cation channels with variable degree of Ca(2+)-permeability. The 28 mammalian TRP channel proteins can be grouped into six subfamilies: canonical, vanilloid, melastatin, ankyrin, polycystic, and mucolipin TRPs. The majority of these TRP channels are expressed in different cell types including both excitable and nonexcitable cells of the cardiovascular system. Unlike voltage-gated ion channels, TRP channels do not have a typical voltage sensor, but instead can sense a variety of other stimuli including pressure, shear stress, mechanical stretch, oxidative stress, lipid environment alterations, hypertrophic signals, and inflammation products. By integrating multiple stimuli and transducing their activity to downstream cellular signal pathways via Ca(2+) entry and/or membrane depolarization, TRP channels play an essential role in regulating fundamental cell functions such as contraction, relaxation, proliferation, differentiation, and cell death. With the use of targeted deletion and transgenic mouse models, recent studies have revealed that TRP channels are involved in numerous cellular functions and play an important role in the pathophysiology of many diseases in the cardiovascular system. Moreover, several TRP channels are involved in inherited diseases of the cardiovascular system. This review presents an overview of current knowledge concerning the physiological functions of TRP channels in the cardiovascular system and their contributions to cardiovascular diseases. Ultimately, TRP channels may become potential therapeutic targets for cardiovascular diseases.

Indexed as

AnimalsCardiovascular SystemHeart DiseasesHumansSignal TransductionTransient Receptor Potential ChannelsTransient Receptor Potential ChannelsCa2+ signalingheart diseasespathogenesisTRP channelsvascular disorders

Identifiers

PMID25416190
PMCPMC4312948
OpenAlexW2058909770

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.