Evidence map›Paper›PMID 23103495›Full record

ArticleAmerican journal of physiology. Heart and circulatory physiology2013

Identification of L- and T-type Ca2+ channels in rat cerebral arteries: role in myogenic tone development.

Rasha R Abd El-Rahman, Osama F Harraz, Suzanne E Brett, Yana Anfinogenova, Rania E Mufti, Daniel Goldman, Donald G Welsh

Abstract read
In one paragraph

Article in American journal of physiology. Heart and circulatory physiology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers.

0numbers the graph read from it
0cells of the map it votes in
55citing 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

55 citing papers in PubMed.

  1. Review
  2. A pericyte chloride clamp mechanism governs capillary control of cerebral blood flow.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Electro-metabolic signaling.The Journal of general physiology · 2024
    Article
  9. The T-type calcium channelosome.Pflugers Archiv : European journal of physiology · 2024
    Review
  10. Review
  11. CaScientific reports · 2023
    Article
  12. Impact of aging on vascular ion channels: perspectives and knowledge gaps across major organ systems.American journal of physiology. Heart and circulatory physiology · 2023
    Review
  13. Vascular mechanotransduction.Physiological reviews · 2023
    Review
  14. Review
  15. Oxidative Regulation of Vascular CaAntioxidants (Basel, Switzerland) · 2022
    Review
  16. Review
  17. Article
  18. Review
  19. Vascular calcium signalling and ageing.The Journal of physiology · 2021
    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

7 authors.

Rasha R Abd El-RahmanHotchkiss Brain and Libin Cardiovascular Research Institute and Department of Physiology and Pharmacology, University of Calgary, Alberta, Canada.
Osama F Harraz
Suzanne E Brett
Yana Anfinogenova
Rania E Mufti
Daniel Goldman
Donald G Welsh

Funding

Canadian Institutes of Health Research
6 · The paper itself

Abstract

L-type Ca(2+) channels are broadly expressed in arterial smooth muscle cells, and their voltage-dependent properties are important in tone development. Recent studies have noted that these Ca(2+) channels are not singularly expressed in vascular tissue and that other subtypes are likely present. In this study, we ascertained which voltage-gated Ca(2+) channels are expressed in rat cerebral arterial smooth muscle and determined their contribution to the myogenic response. mRNA analysis revealed that the α(1)-subunit of L-type (Ca(v)1.2) and T-type (Ca(v)3.1 and Ca(v)3.2) Ca(2+) channels are present in isolated smooth muscle cells. Western blot analysis subsequently confirmed protein expression in whole arteries. With the use of patch clamp electrophysiology, nifedipine-sensitive and -insensitive Ba(2+) currents were isolated and each were shown to retain electrical characteristics consistent with L- and T-type Ca(2+) channels. The nifedipine-insensitive Ba(2+) current was blocked by mibefradil, kurtoxin, and efonidpine, T-type Ca(2+) channel inhibitors. Pressure myography revealed that L-type Ca(2+) channel inhibition reduced tone at 20 and 80 mmHg, with the greatest effect at high pressure when the vessel is depolarized. In comparison, the effect of T-type Ca(2+) channel blockade on myogenic tone was more limited, with their greatest effect at low pressure where vessels are hyperpolarized. Blood flow modeling revealed that the vasomotor responses induced by T-type Ca(2+) blockade could alter arterial flow by ∼20-50%. Overall, our findings indicate that L- and T-type Ca(2+) channels are expressed in cerebral arterial smooth muscle and can be electrically isolated from one another. Both conductances contribute to myogenic tone, although their overall contribution is unequal.

Indexed as

VasoconstrictionVasodilationAnimalsBlood PressureBlotting, WesternCalcium Channel BlockersCalcium Channels, L-TypeCalcium Channels, T-TypeCerebral ArteriesComputer SimulationDose-Response Relationship, DrugFemaleGene Expression RegulationMembrane PotentialsModels, CardiovascularMuscle, Smooth, VascularCacna1c protein, ratCacna1g protein, ratCacna1h protein, ratCalcium Channel BlockersCalcium Channels, L-TypeCalcium Channels, T-TypeRNA, Messenger

Identifiers

PMID23103495
PMCPMC3543679

What OpenQuestion holds

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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.