Evidence map›Paper›PMID 35076184›Full record

ArticlePhysiological reports2022

Action potential responses to changes in stimulation frequency and isoproterenol in rat ventricular myocytes.

Luke A Howlett, Hannah M Kirton, Moza M Al-Owais, Derek Steele, Matthew K Lancaster

Abstract read
In one paragraph

Article in Physiological reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. 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

5 authors.

Luke A HowlettFaculty of Biological Sciences, University of Leeds, Leeds, UK.ORCID 0000-0002-7786-5569
Hannah M KirtonFaculty of Biological Sciences, University of Leeds, Leeds, UK.
Moza M Al-OwaisFaculty of Biological Sciences, University of Leeds, Leeds, UK.
Derek SteeleFaculty of Biological Sciences, University of Leeds, Leeds, UK.
Matthew K LancasterFaculty of Biological Sciences, University of Leeds, Leeds, UK.

Funding

British Heart Foundation PG/19/68/34614British Heart Foundation RG/11/10/28924British Heart Foundation RG/16/6/32233
6 · The paper itself

Abstract

purposeCurrent understanding of ventricular action potential adaptation to physiological stress is generally based on protocols using non-physiological rates and conditions isolating rate effects from escalating adrenergic stimulation. To permit refined understanding, ventricular action potentials were assessed across physiological pacing frequencies in the presence and absence of adrenergic stimuli. Isolated and combined effects were analyzed to assess their ability to replicate in-vivo responses.

methodsSteady-state action potentials from ventricular myocytes isolated from male Wistar rats (3 months; N = 8 animals) were recorded at 37°C with steady-state pacing at 1, 2, 4, 6, 8 and 10 Hz using whole-cell patch-clamp. Action potential repolarization to 25, 50, 75, 90 and 100% of full repolarization (APD

resultsA Repeated measures ANOVA found APD

conclusionThese results demonstrate modest action potential shortening in response to adrenergic stimulation and elevations in pacing beyond physiological resting rates. Our findings indicate changes in action potential plateau and late repolarization predominantly underlie simulated exercise responses in the rat heart. This work provides novel action potential reference data and will help model cardiac responses to physiological stimuli in the rat heart via computational techniques.

Indexed as

Heart VentriclesMyocytes, CardiacAction PotentialsAnimalsIsoproterenolMaleRatsRats, WistarIsoproterenolaction potentialadrenergic responsecardiovascularElectrophysiologyexercise

Identifiers

PMID35076184
PMCPMC8787729

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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.