Evidence map›Paper›PMID 16120184›Full record

ReviewClinical and experimental pharmacology & physiology2005

Emerging functions of 10 types of TRP cationic channel in vascular smooth muscle.

David J Beech

Open access · bronzeAbstract readReview
In one paragraph

Review in Clinical and experimental pharmacology & physiology, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 40 papers.

0numbers the graph read from it
0cells of the map it votes in
40citing papers in PubMed
4.1field-weighted citation impact, top 5% 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

40 citing papers in PubMed, 98 citations in OpenAlex.

  1. Transient receptor potential melastatin 8 channel involvement in the regulation of vascular tone.American journal of physiology. Heart and circulatory physiology · 2009
    Trial
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Regulator of G Protein Signaling 2: A Versatile Regulator of Vascular Function.Progress in molecular biology and translational science · 2015
    Review
  8. Review
  9. Article
  10. Targeted STIM deletion impairs calcium homeostasis, NFAT activation, and growth of smooth muscle.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2013
    Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Canonical transient receptor potential channels in diabetes.Experimental biology and medicine (Maywood, N.J.) · 2012
    Review
  16. Article
  17. Article
  18. Review
  19. Calcium oscillations.Cold Spring Harbor perspectives in biology · 2011
    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

1 author at 1 institution in 1 country.

David J BeechMembrane Biology Research Group, School of Biomedical Sciences, University of Leeds, Leeds, UK. d.j.beech@leeds.ac.uk
University of Leeds · GB

Funding

Wellcome Trust 060988
6 · The paper itself

Abstract

1. The influx of Ca2+, Mg2+ and Na+ and the efflux of K+ have central importance for the function and survival of vascular smooth muscle cells, but progress in understanding the influx/efflux pathways has been restricted by a lack of identification of the genes underlying many of the non-voltage-gated cationic channels. 2. The present review highlights evidence suggesting the genes are mammalian homologues of the Transient Receptor Potential (TRP) gene of the fruit-fly Drosophila. The weight of evidence supports roles for TRPC1, TRPP2/1 and TRPC6, but recent studies point also to TRPC3, TRPC4/5, TRPV2, TRPM4 and TRPM7. 3. Activity of these TRP channels is suggested to modulate contraction and sense changes in intracellular Ca2+ storage, G-protein-coupled receptor activation and osmotic stress. Roles in relation to myogenic tone, actions of vasoconstrictors substances, Mg2+ homeostasis and the vascular injury response are suggested. 4. Knowledge that TRP channels are relevant to vascular smooth muscle cells in both their contractile and proliferative phenotypes should pave the way for a better understanding of vascular biology and provide the basis for the discovery of a new set of therapeutic agents targeted to vascular disease.

Indexed as

AnimalsIon ChannelsMuscle, Smooth, VascularIon Channels

Identifiers

PMID16120184
PMCPMC2645062
OpenAlexW1990813305

What OpenQuestion holds

Textmetadata
LicenceTDM
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.