Evidence map›Paper›PMID 25595366›Full record

ArticleAmerican journal of physiology. Heart and circulatory physiology2015

Cardiac tissue slices: preparation, handling, and successful optical mapping.

Ken Wang, Peter Lee, Gary R Mirams, Padmini Sarathchandra, Thomas K Borg, David J Gavaghan, Peter Kohl, Christian Bollensdorff

Open access · hybridAbstract read
In one paragraph

Article in American journal of physiology. Heart and circulatory physiology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
4.0field-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

42 citing papers in PubMed, 64 citations in OpenAlex.

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  16. Review
  17. Review
  18. Multiphoton Imaging of CaJournal of clinical medicine · 2021
    Article
  19. Article
  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

8 authors at 3 institutions in 3 countries.

Ken WangDepartment of Computer Science, University of Oxford, Oxford, United Kingdom;
Peter LeeDepartment of Physics, University of Oxford, Clarendon Laboratory, Oxford, United Kingdom;
Gary R MiramsDepartment of Computer Science, University of Oxford, Oxford, United Kingdom;
Padmini SarathchandraHarefield Heart Science Centre, National Heart and Lung Institute, Imperial College London, Middlesex, United Kingdom;
Thomas K BorgDepartment of Regenerative Medicine and Cell Biology, University of South Carolina School of Medicine, Charleston, South Carolina; and.
David J GavaghanDepartment of Computer Science, University of Oxford, Oxford, United Kingdom;
Peter KohlDepartment of Computer Science, University of Oxford, Oxford, United Kingdom; Harefield Heart Science Centre, National Heart and Lung Institute, Imperial College London, Middlesex, United Kingdom;
Christian BollensdorffHarefield Heart Science Centre, National Heart and Lung Institute, Imperial College London, Middlesex, United Kingdom; Qatar Cardiovascular Research Center, Qatar Foundation, Doha, Qatar cbollensdorff@qf.org.qa.ORCID http://orcid.org/0000-0002-6333-4791
University of Oxford · GBHarefield Hospital · GBMedical University of South Carolina · US

Funding

British Heart Foundation FS/12/17/29532British Heart Foundation NH/13/1/30238National Centre for the Replacement, Refinement and Reduction of Animals in Research NC/K001337/1Wellcome Trust 101222
6 · The paper itself

Abstract

Cardiac tissue slices are becoming increasingly popular as a model system for cardiac electrophysiology and pharmacology research and development. Here, we describe in detail the preparation, handling, and optical mapping of transmembrane potential and intracellular free calcium concentration transients (CaT) in ventricular tissue slices from guinea pigs and rabbits. Slices cut in the epicardium-tangential plane contained well-aligned in-slice myocardial cell strands ("fibers") in subepicardial and midmyocardial sections. Cut with a high-precision slow-advancing microtome at a thickness of 350 to 400 μm, tissue slices preserved essential action potential (AP) properties of the precutting Langendorff-perfused heart. We identified the need for a postcutting recovery period of 36 min (guinea pig) and 63 min (rabbit) to reach 97.5% of final steady-state values for AP duration (APD) (identified by exponential fitting). There was no significant difference between the postcutting recovery dynamics in slices obtained using 2,3-butanedione 2-monoxime or blebistatin as electromechanical uncouplers during the cutting process. A rapid increase in APD, seen after cutting, was caused by exposure to ice-cold solution during the slicing procedure, not by tissue injury, differences in uncouplers, or pH-buffers (bicarbonate; HEPES). To characterize intrinsic patterns of CaT, AP, and conduction, a combination of multipoint and field stimulation should be used to avoid misinterpretation based on source-sink effects. In summary, we describe in detail the preparation, mapping, and data analysis approaches for reproducible cardiac tissue slice-based investigations into AP and CaT dynamics.

Indexed as

Calcium SignalingCold TemperatureAction PotentialsAnimalsCardiac Pacing, ArtificialFemaleGuinea PigsIn Vitro TechniquesKineticsMaleMicrotomyMyocardiumPerfusionRabbitsRecovery of FunctionSignal Processing, Computer-Assistedhearthigh spatial resolutionlive tissue slicesmultiparametricoptical mappingvoltage- and calcium-sensitive dyes

Identifiers

PMID25595366
PMCPMC4551126
OpenAlexW2147038961

What OpenQuestion holds

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LicenceCC BY
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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.