Evidence map›Paper›PMID 16669348›Full record

ArticleJournal of physiology and biochemistry2005

Collaborative effect of SERCA and PMCA in cytosolic calcium homeostasis in human platelets.

P C Redondo, J A Rosado, J A Pariente, G M Salido

Abstract read
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In one paragraph

Article in Journal of physiology and biochemistry, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
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

8 citing papers in PubMed.

  1. Antioxidant potential of nanomaterials.Turkish journal of biology = Turk biyoloji dergisi · 2023
    Review
  2. Review
  3. Article
  4. TRPs in Pain Sensation.Frontiers in physiology · 2017
    Review
  5. Article
  6. Article
  7. Article
  8. 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

4 authors.

P C RedondoDepartment of Physiology, University of Extremadura, 10071 Cáceres, Spain. pcr@unex.es
J A Rosado
J A Pariente
G M Salido

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Intracellular free Ca2+ concentration ([Ca2+]c) is finely regulated by several mechanisms that either increase or reduce [Ca2+]c. Two different Ca2+ pumps have been described so far as the main mechanisms for Ca2+ removal from the cytosol, either by its sequestration into the stores, mediated by the sarco(endo)plasmic reticulum Ca2+-ATPase (SERCA) or by Ca2+ extrusion to the extracellular medium, by the plasma membrane Ca2+-ATPase (PMCA). We have used inhibitors of these pumps to analyze their Ca2+ clearance efficacy in human platelets stimulated by the physiological agonist thrombin. Results demonstrate that, after platelet stimulation with thrombin, activation of SERCA precedes that of PMCA, although the ability of PMCA to remove Ca2+ from the cytosol last longer than that of SERCA. The efficacy of SERCA and PMCA removing Ca2+ from the cytosol is reduced when the concentration of thrombin increases. This phenomenon correlates with the greater increase in [Ca2+]c induced by higher concentrations of thrombin, which further confirms that SERCA and PMCA activities are regulated by [Ca2+]c.

Indexed as

Blood PlateletsCalciumCalcium-Transporting ATPasesCation Transport ProteinsCytosolDose-Response Relationship, DrugHomeostasisHumansPlasma Membrane Calcium-Transporting ATPasesPlatelet ActivationSarcoplasmic Reticulum Calcium-Transporting ATPasesThrombinTime FactorsCalciumCalcium-Transporting ATPasesCation Transport ProteinsPlasma Membrane Calcium-Transporting ATPasesSarcoplasmic Reticulum Calcium-Transporting ATPasesThrombin

Identifiers

PMID16669348

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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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.