Evidence map›Paper›PMID 10713963›Full record

ArticleThe Journal of physiology2000

Mitochondrial Ca2+ homeostasis during Ca2+ influx and Ca2+ release in gastric myocytes from Bufo marinus.

R M Drummond, T C Mix, R A Tuft, J V Walsh, F S Fay

Open access · bronzeAbstract 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 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.6field-weighted citation impact, top 9% 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

21 citing papers in PubMed, 56 citations in OpenAlex.

  1. Isochlorogenic Acid C andJournal of microbiology and biotechnology · 2025
    Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. The mitochondrial calcium uniporter: mice can live and die without it.Journal of molecular and cellular cardiology · 2015
    Review
  7. Review
  8. Mitochondrial motility and vascular smooth muscle proliferation.Arteriosclerosis, thrombosis, and vascular biology · 2012
    Article
  9. Mitochondrial regulation of cytosolic Ca²⁺ signals in smooth muscle.Pflugers Archiv : European journal of physiology · 2012
    Review
  10. Article
  11. Structural and functional link between the mitochondrial network and the endoplasmic reticulum.The international journal of biochemistry & cell biology · 2009
    Review
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Presynaptic mitochondrial calcium sequestration influences transmission at mammalian central synapses.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2002
    Article
  19. Article
  20. 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

5 authors at 1 institution in 1 country.

R M DrummondDepartment of Physiology, University of Massachusetts Medical Center, Worcester 01605, USA. robert.drummond@umassmed.edu
T C Mix
R A Tuft
J V Walsh
F S Fay
University of Massachusetts Chan Medical School · US

Funding

LOCAL CA++ SIGNALING IN SMOOTH MUSCLER01HL061297 · NHLBI · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI WALSH, JOHN V · 1999 to 2008
$3.7M
SMOOTH MUSCLE FUNCTION--CELLULAR &MOLECULAR MECHANISMSP01HL047530 · NHLBI · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI FOGARTY, KEVIN E · 1993 to 1997
–
NHLBI NIH HHS HL 47530NHLBI NIH HHS HL 61297-01NHLBI NIH HHS R01 HL061297
6 · The paper itself

Abstract

1. The Ca(2+)-sensitive fluorescent indicator rhod-2 was used to monitor mitochondrial Ca2+ concentration ([Ca2+]m) in gastric smooth muscle cells from Bufo marinus. In some studies, fura-2 was used in combination with rhod-2, allowing simultaneous measurement of cytoplasmic Ca2+ concentration ([Ca2+]i) and [Ca2+]m, respectively. 2. During a short train of depolarizations, which causes Ca2+ influx from the extracellular medium, there was an increase in both [Ca2+]i and [Ca2+]m. The half-time (t1/2) to peak for the increase in [Ca2+]m was considerably longer than the t1/2 to peak for the increase in [Ca2+]i. [Ca2+]m remained elevated for tens of seconds after [Ca2+]i had returned to its resting value. 3. Stimulation with caffeine, which causes release of Ca2+ from the sarcoplasmic reticulum (SR), also produced increases in both [Ca2+]i and [Ca2+]m. The values of t1/2 to peak for the increase in [Ca2+] in both cytoplasm and mitochondria were similar; however, [Ca2+]i returned to baseline values much faster than [Ca2+]m. 4. Using a wide-field digital imaging microscope, changes in [Ca2+]m were monitored within individual mitochondria in situ, during stimulation of Ca2+ influx or Ca2+ release from the SR. 5. Mitochondrial Ca2+ uptake during depolarizing stimulation caused depolarization of the mitochondrial membrane potential. The mitochondrial membrane potential recovered considerably faster than the recovery of [Ca2+]m. 6. This study shows that Ca2+ influx from the extracellular medium and Ca2+ release from the SR are capable of increasing [Ca2+]m in smooth muscle cells. The efflux of Ca2+ from the mitochondria is a slow process and appears to be dependent upon the amount of Ca2+ in the SR.

Indexed as

AnimalsBufo marinusCaffeineCalciumCells, CulturedCytoplasmElectric StimulationFluorescent DyesHeterocyclic Compounds, 3-RingHomeostasisIntracellular MembranesMembrane PotentialsMicroscopy, VideoMitochondriaMuscle, SmoothPatch-Clamp TechniquesCaffeineCalciumFluorescent DyesHeterocyclic Compounds, 3-Ringrhod-2

Identifiers

PMID10713963
PMCPMC2269764
OpenAlexW2126735173

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.