Evidence map›Paper›PMID 42488573›Full record

ArticleFrontiers in pharmacology2026

A modification of retrograde Langendorff-perfusion to increase the yield of Ca

Jan Peter Reinhardt, Yasmina Steins, Luca Bartolomeo Tardio, Max Gieske, Paul Pauls, Matthias Dodo Seidl, Uwe Kirchhefer, Lars Eckardt, Frank Ulrich Müller, Jan Sebastian Schulte

Abstract read
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Article in Frontiers in pharmacology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

10 authors.

Jan Peter ReinhardtInstitute of Pharmacology and Toxicology, University of Münster, Münster, Germany.
Yasmina SteinsInstitute of Pharmacology and Toxicology, University of Münster, Münster, Germany.
Luca Bartolomeo TardioInstitute of Pharmacology and Toxicology, University of Münster, Münster, Germany.
Max GieskeInstitute of Pharmacology and Toxicology, University of Münster, Münster, Germany.
Paul PaulsInstitute of Pharmacology and Toxicology, University of Münster, Münster, Germany.
Matthias Dodo SeidlInstitute of Pharmacology and Toxicology, University of Münster, Münster, Germany.
Uwe KirchheferInstitute of Pharmacology and Toxicology, University of Münster, Münster, Germany.
Lars EckardtDepartment of Cardiology II - Electrophysiology, University Hospital Münster, Münster, Germany.
Frank Ulrich MüllerInstitute of Pharmacology and Toxicology, University of Münster, Münster, Germany.
Jan Sebastian SchulteInstitute of Pharmacology and Toxicology, University of Münster, Münster, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objective: Langendorff-perfusion is an established method to isolate cardiomyocytes from cardiac tissue for the investigation of cellular remodelling in cardiovascular diseases. Despite the existence of several protocols for isolation of murine atrial cardiomyocytes (aCM), extraction of a sufficient yield of Ca Methods: The effect of an additional ventricular ligature during Langendorff-perfusion on the yield of isolated aCM was evaluated in mice with cardiomyocyte-specific overexpression of CREM-IbΔC-X, a mouse model of pronounced atrial dilatation and spontaneous onset atrial fibrillation compared to littermate controls. Results: Atria with overexpression of CREM-IbΔC-X exhibited dilatation, increased mass and enhanced fibrosis. From such remodelled atria, we observed significantly lower extractions both of total and morphologically intact aCM compared to wildtype. The additional ventricular ligature did not affect total aCM yield in wildtype, but in fibrotic atria; the total aCM count was significantly increased (26 ± 4 vs. 15 ± 3 aCM/10 µL). Importantly, the number of morphologically intact, Ca Conclusion: The modification of an established Langendorff-perfusion protocol for aCM isolation by an additional ventricular ligature is associated with a numerically higher yield of morphologically intact, Ca

Indexed as

atrial cardiomyocyte isolationcardiac remodellingcell isolationcellular electrophysiologylangendorff retrograde perfusionmouse heart

Identifiers

PMID42488573
PMCPMC13389159

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