Evidence map›Paper›PMID 10747180›Full record

ArticleThe Journal of physiology2000

Multiple pathways responsible for the stretch-induced increase in Ca2+ concentration in toad stomach smooth muscle cells.

M T Kirber, A Guerrero-Hernández, D S Bowman, K E Fogarty, R A Tuft, J J Singer, F S Fay

Open access · greenAbstract read
In one paragraph

Article in The Journal of physiology, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.7field-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

14 citing papers in PubMed, 48 citations in OpenAlex.

  1. Stretch-Induced Increase in CaJournal of the American Heart Association · 2025
    Article
  2. Article
  3. Mechanotransduction in gastrointestinal smooth muscle cells: role of mechanosensitive ion channels.American journal of physiology. Gastrointestinal and liver physiology · 2021
    Review
  4. Role of BKBioMed research international · 2016
    Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Stretch-induced calcium release in smooth muscle.The Journal of general physiology · 2002
    Article
  13. Article
  14. Visualization of Ca2+ entry through single stretch-activated cation channels.Proceedings of the National Academy of Sciences of the United States of America · 2002
    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 2 institutions in 2 countries.

M T KirberDepartment of Physiology, University of Massachusetts Medical School, Worcester, MA 01655, USA.
A Guerrero-Hernández
D S Bowman
K E Fogarty
R A Tuft
J J Singer
F S Fay
University of Massachusetts Chan Medical School · USBrown University · US

Funding

GENERATION AND REGULATION OF FORCE IN SMOOTH MUSCLER01HL014523 · NHLBI · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI TUFT, RICHARD ALLAN · 1985 to 1996
–
GENERATION AND REGULATION OF FORCE IN SMOOTH MUSCLER37HL014523 · NHLBI · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI FAY, FREDRIC S · 1990 to 1996
–
NHLBI NIH HHS HL-14523
6 · The paper itself

Abstract

1. A digital imaging microscope with fura-2 as the Ca2+ indicator was used to determine the sources for the rise in intracellular calcium concentration ([Ca2+]i) that occurs when the membrane in a cell-attached patch is stretched. Unitary ionic currents from stretch-activated channels and [Ca2+]i images were recorded simultaneously. 2. When suction was applied to the patch pipette to stretch a patch of membrane, Ca2+-permeable cation channels (stretch-activated channels) opened and a global increase in [Ca2+]i occurred, as well as a greater focal increase in the vicinity of the patch pipette. The global changes in [Ca2+]i occurred only when stretch-activated currents were sufficient to cause membrane depolarization, as indicated by the reduction in amplitude of the unitary currents. 3. When Ca2+ was present only in the pipette solution, just the focal change in [Ca2+]i was obtained. This focal change was not seen when the contribution from Ca2+ stores was eliminated using caffeine and ryanodine. 4. These results suggest that the opening of stretch-activated channels allows ions, including Ca2+, to enter the cell. The entry of positive charge triggers the influx of Ca2+ into the cell by causing membrane depolarization, which presumably activates voltage-gated Ca2+ channels. The entry of Ca2+ through stretch-activated channels is also amplified by Ca2+ release from internal stores. This amplification appears to be greater than that obtained by activation of whole-cell Ca2+ currents. These multiple pathways whereby membrane stretch causes a rise in [Ca2+]i may play a role in stretch-induced contraction, which is a characteristic of many smooth muscle tissues.

Indexed as

AnimalsBufo marinusCalciumCalcium ChannelsIn Vitro TechniquesMembrane PotentialsMuscle ContractionMuscle, SmoothPatch-Clamp TechniquesStomachCalciumCalcium Channels

Identifiers

PMID10747180
PMCPMC2269860
OpenAlexW2166098430

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.