Evidence map›Paper›PMID 10420017›Full record

ArticleThe Journal of physiology1999

Local and cellular Ca2+ transients in smooth muscle of pressurized rat resistance arteries during myogenic and agonist stimulation.

V A Miriel, J R Mauban, M P Blaustein, W G Wier

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of physiology, 1999. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed
3.9field-weighted citation impact, top 6% 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

56 citing papers in PubMed, 135 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. CaScientific reports · 2023
    Article
  6. Review
  7. Review
  8. Review
  9. Spatial-temporal patterning of CaSeminars in cell & developmental biology · 2019
    Review
  10. Calcium signals that determine vascular resistance.Wiley interdisciplinary reviews. Systems biology and medicine · 2019
    Review
  11. Voltage-gated CaAmerican journal of physiology. Heart and circulatory physiology · 2018
    Article
  12. Article
  13. Article
  14. AlphaPhysiological reports · 2018
    Article
  15. Article
  16. Regional heterogeneity in the mechanisms of myogenic tone in hamster arterioles.American journal of physiology. Heart and circulatory physiology · 2017
    Article
  17. Review
  18. 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

4 authors at 1 institution in 1 country.

V A MirielDepartment of Physiology, School of Medicine, University of Maryland, 655 West Baltimore Street, Baltimore, MD 21201, USA.
J R Mauban
M P Blaustein
W G Wier
University of Maryland, Baltimore · US

Funding

Interdisciplinary Training Program Muscle BiologyT32AR007592 · NIAMS · UNIVERSITY OF MARYLAND BALTIMORE · PI Aikaterini Kontrogianni-Konstantopoulos · 1996 to 2026
$11.7M
CALCIUM AND SODIUM TRANSPORT IN VASCULAR SMOOTH MUSCLER01HL045215 · NHLBI · UNIVERSITY OF MARYLAND BALTIMORE · PI BLAUSTEIN, MORDECAI P, HAMLYN, JOHN · 1990 to 2012
$4.1M
LOCAL CONTROL OF CARDIAC EXCITATION/CONTRACTION COUPLINGR01HL055280 · NHLBI · UNIVERSITY OF MARYLAND BALTIMORE · PI WIER, WITHROW G · 1996 to 2000
$217k
NHLBI NIH HHS HL-45215NHLBI NIH HHS HL-55280NHLBI NIH HHS R01 HL045215NIAMS NIH HHS AR-07592NIAMS NIH HHS T32 AR007592
6 · The paper itself

Abstract

1. Confocal laser scanning microscopy was used to visualize Ca2+ transients in the vascular smooth muscle cells (VSMC) of intact, pressurized rat mesenteric resistance arteries loaded with fluorescent calcium indicators. Vasoconstriction was assessed by measuring inner arterial diameter. All arteries were studied at 70 mmHg intralumenal pressure and 37 C. 2. In the control condition of myogenic tone the arteries were constricted to 62 % (n = 10) of their passive diameter (p.d.). The [Ca2+]i in most VSMC of these arteries was constant over time. In a small percentage (< 10 %) of cells in each artery, [Ca2+]i oscillated regularly. Local calcium transients (Ca2+ sparks) were observed in five arteries studied with confocal linescan imaging. 3. Activation of alpha-adrenoceptors by phenylephrine (PE, 1.0 microM) induced further vasoconstriction of pressurized arteries (to 27 % of p.d.). In this condition, [Ca2+]i oscillations were prominent in a large percentage (83 %) of the VSMC. The Ca2+ oscillations ranged in frequency from 4 to 22 min-1, and were usually asynchronous between cells. 4. High [KCl]o (65 mM) induced nearly comparable vasoconstriction to PE (37 % of p.d.) but [Ca2+]i oscillated in only about 13 % of cells in each artery. 5. Block of L-type Ca2+ channels (with nifedipine) in arteries activated by PE caused nearly full vasodilatation, but did not abolish the Ca2+ oscillations. Subsequent block of the sarcoplasmic reticulum Ca2+ pump (with cyclopiazonic acid) abolished Ca2+ oscillations in all cells. 6. We conclude that Ca2+ entering VSMC via L-type Ca2+ channels has an obligatory role in force development, both in myogenic tone and during alpha1-adrenoceptor activation. The oscillatory pattern of [Ca2+]i that persists in the absence of Ca2+ entry via L-type Ca2+ channels is ineffective in activating contraction.

Indexed as

Adrenergic alpha-AgonistsAnimalsArteriesCalcium Channel BlockersCalcium ChannelsCalcium Channels, L-TypeCalcium SignalingFluorescent DyesIndolesIn Vitro TechniquesMaleMicroscopy, ConfocalMuscle, Smooth, VascularMuscle TonusNifedipinePhenylephrineAdrenergic alpha-AgonistsCalcium Channel BlockersCalcium ChannelsCalcium Channels, L-Typecyclopiazonic acidFluorescent DyesIndolesNifedipinePhenylephrinePotassium ChlorideVasodilator Agents

Identifiers

PMID10420017
PMCPMC2269448
OpenAlexW2088919308

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.