Evidence map›Paper›PMID 41397434›Full record

ArticleJournal of the American Association for Laboratory Animal Science : JAALAS2025

Refining the Guinea Pig (Cavia porcellus) Cryo-Injury Model for Cardiac Regeneration and Functional Characterization.

Marie E Nehring, Constantin von Bibra, Birgit Geertz, Gesa Roessler, Yoram Etzion, Liesa Castro, Or Levi, Shira Burg, Bernhard Hiebl, Thomas Eschenhagen and 1 more

Abstract read
In one paragraph

Article in Journal of the American Association for Laboratory Animal Science : JAALAS, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

11 authors.

Marie E Nehring1Department of Experimental Pharmacology and Toxicology, University Medical Center Hamburg-Eppendorf, Germany.
Constantin von Bibra3Institute for Animal Hygiene, Animal Welfare and Farm Animal Behavior, Stiftung Tieraerztliche Hochschule Hannover, University of Veterinary Medicine, Hannover, Germany.
Birgit Geertz1Department of Experimental Pharmacology and Toxicology, University Medical Center Hamburg-Eppendorf, Germany.
Gesa Roessler1Department of Experimental Pharmacology and Toxicology, University Medical Center Hamburg-Eppendorf, Germany.
Yoram Etzion6Cardiac Arrhythmia Research Laboratory, Department of Physiology and Cell Biology, Faculty of Health Sciences, Ben-Gurion University of the Negev, Beer-Sheva, Israel.
Liesa Castro8Department of Cardiovascular Surgery, University Heart and Vascular Center Hamburg, Hamburg, Germany.
Or Levi6Cardiac Arrhythmia Research Laboratory, Department of Physiology and Cell Biology, Faculty of Health Sciences, Ben-Gurion University of the Negev, Beer-Sheva, Israel.
Shira Burg9Department of Physiology and Pharmacology, Sackler Faculty of Medicine and Sagol School of Neurosciences, Tel Aviv University, Tel Aviv, Israel.
Bernhard Hiebl3Institute for Animal Hygiene, Animal Welfare and Farm Animal Behavior, Stiftung Tieraerztliche Hochschule Hannover, University of Veterinary Medicine, Hannover, Germany.
Thomas Eschenhagen1Department of Experimental Pharmacology and Toxicology, University Medical Center Hamburg-Eppendorf, Germany.
Florian Weinberger1Department of Experimental Pharmacology and Toxicology, University Medical Center Hamburg-Eppendorf, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Guinea pigs have been a standard model in cardiovascular pharmacology and physiology research, but the advent of transgenic models has largely replaced them with mouse and rat models. However, guinea pigs remain important models in cardiac electrophysiology, drug-induced arrhythmias, or atherosclerosis research, and they have recently gained importance for studying one specific research question, that is, transplantation of pluripotent stem cell derived cardiomyocytes to repair the cryo-injured heart. Their human-like cardiac electrophysiology, together with their small size that facilitates handling and housing, make guinea pigs a valuable experimental model for these studies. However, repeated open heart surgeries in guinea pigs are technically demanding and accompanied by high mortality. In this study, we retrospectively examined sequential protocol modifications and describe how protocol refinements led to improved survival rates. Cryo-injury was performed in female Dunkin-Hartley guinea pigs under general anesthesia with a liquid nitrogen-cooled probe via a lateral thoracotomy. Cells were transplanted during a second surgery 7 days later. We analyzed data from up to 558 animals to determine mortality rates and morphologic and functional parameters. Initial studies revealed a mortality rate of ∼50%. Sequential modifications led to a significant reduction, with the refined protocol achieving a perioperative mortality rate of ∼30%. The procedures were completed in <35 minutes, and survival rates for the observation period (up to 8 weeks) were 70%. Scar size was evaluated in 144 (4 weeks, n = 92; 8 weeks, n = 52) animals and showed a significant, but shallow correlation with echocardiographically determined heart function. Taken together, refined surgery protocols allow safe and reproducible cryo-injury with subsequent cell injections in guinea pigs with an improved mortality rate.

Indexed as

bw, body weightCM, cardiomyocytesEHT, engineered heart tissueFAC, fractional area changeFS, fractional shorteningLAD, left anterior descending coronary arteryLV, left ventricleMMF, medetomidine-midazolam-fentanyl

Identifiers

PMID41397434
PMCPMC12878998

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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.