Skip to content

Study · Animal study (in vivo) · rat · 2026

7 results

Differential effects of semaglutide and colchicine on atrial remodeling in rats with reduced ejection fraction after myocardial infarction.

Levi O, Dalal N, Komissar A, Moldavsky D, Khamaisi S, Elyagon S, Murninkas M, Eliyahu A, Burg S, Attali B, Makarovsky D, Lichtenstein A and 6 more

Show all authors

Gradwohl G, Tsaban G, Kakzanov Y, Laish-Farkash A, Etzion S, Etzion Y

Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology1 May 2026Cited by 2 (Europe PMC)

Summary

The text of this summary is not shown here, because the article license does not allow reuse. Read it at the source (opens in a new tab)

Text rights: CC BY-NC. Results still quote short attributed sentences.

Results from this study7

7 results from studies that gave the peptide. No result from this study comes from people.

  1. 01AnimalAnimal study (in vivo)Efficacy outcome

    In post-infarction rats with reduced ejection fraction, semaglutide reduced atrial fibrillation inducibility.

    In plain wordsIn rats with heart damage after a heart attack, semaglutide made atrial fibrillation harder to trigger.

    Outcome
    DecreaseAtrial fibrillation inducibility
    Study

    ratn: not reported in source

    Post-myocardial infarction rats with reduced ejection fraction
    Comparator
    Vehicle
    Outcome group
    Heart function · Cardiovascular
    Studied dose
    40 µg/kg every 72 h · subcutaneous · 21 daysAs given in this study (rat).

    Source sentences

    Summary
    Both semaglutide and colchicine reduced AF inducibility
    1 context sentence
    Summary · context
    One-week post-MI, animals with left ventricular ejection fraction ≤40% were randomized to semaglutide (40 µg/kg subcutaneously every 72 h), colchicine (100 µg/kg intraperitoneally daily), or vehicle for 21 days.
  2. 02AnimalAnimal study (in vivo)Efficacy outcome

    In post-infarction rats with reduced ejection fraction, semaglutide reduced atrial fibrillation duration.

    In plain wordsIn rats with heart damage after a heart attack, semaglutide shortened episodes of atrial fibrillation.

    Outcome
    DecreaseAtrial fibrillation duration
    Study

    ratn: not reported in source

    Post-myocardial infarction rats with reduced ejection fraction
    Comparator
    Vehicle
    Outcome group
    Heart function · Cardiovascular
    Studied dose
    40 µg/kg every 72 h · subcutaneous · 21 daysAs given in this study (rat).

    Source sentences

    Summary
    Both semaglutide and colchicine reduced AF inducibility and AF duration, whereas semaglutide additionally reduced atrial signal complexity.
    1 context sentence
    Summary · context
    One-week post-MI, animals with left ventricular ejection fraction ≤40% were randomized to semaglutide (40 µg/kg subcutaneously every 72 h), colchicine (100 µg/kg intraperitoneally daily), or vehicle for 21 days.
  3. 03AnimalAnimal study (in vivo)Efficacy outcome

    In post-infarction rats with reduced ejection fraction, semaglutide reduced atrial signal complexity, which colchicine was not reported to do.

    In plain wordsIn rats with heart damage after a heart attack, semaglutide reduced the complexity of atrial electrical signals.

    Outcome
    DecreaseAtrial signal complexity
    Study

    ratn: not reported in source

    Post-myocardial infarction rats with reduced ejection fraction
    Comparator
    Vehicle
    Outcome group
    Heart function · Cardiovascular
    Studied dose
    40 µg/kg every 72 h · subcutaneous · 21 daysAs given in this study (rat).

    Source sentences

    Summary
    whereas semaglutide additionally reduced atrial signal complexity.
    1 context sentence
    Summary · context
    One-week post-MI, animals with left ventricular ejection fraction ≤40% were randomized to semaglutide (40 µg/kg subcutaneously every 72 h), colchicine (100 µg/kg intraperitoneally daily), or vehicle for 21 days.
  4. 04AnimalAnimal study (in vivo)Efficacy outcome

    In post-infarction rats with reduced ejection fraction, semaglutide attenuated atrial fibrosis.

    In plain wordsIn rats with heart damage after a heart attack, semaglutide reduced scarring in the upper heart chambers.

    Outcome
    DecreaseAtrial fibrosis
    Study

    ratn: not reported in source

    Post-myocardial infarction rats with reduced ejection fraction
    Comparator
    Vehicle
    Outcome group
    Heart function · Cardiovascular
    Studied dose
    40 µg/kg every 72 h · subcutaneous · 21 daysAs given in this study (rat).

    Source sentences

    Summary
    Semaglutide attenuated atrial fibrosis
    1 context sentence
    Summary · context
    One-week post-MI, animals with left ventricular ejection fraction ≤40% were randomized to semaglutide (40 µg/kg subcutaneously every 72 h), colchicine (100 µg/kg intraperitoneally daily), or vehicle for 21 days.
  5. 05AnimalAnimal study (in vivo)Mechanism

    In post-infarction rats with reduced ejection fraction, semaglutide suppressed atrial NLRP3 inflammasome expression.

    In plain wordsIn rats with heart damage after a heart attack, semaglutide lowered an inflammation-related protein in the atria.

    Outcome
    DecreaseNLRP3 inflammasome expression
    Study

    ratn: not reported in source

    Post-myocardial infarction rats with reduced ejection fraction
    Comparator
    Vehicle
    Outcome group
    Inflammation markers · Immune and inflammation
    Studied dose
    40 µg/kg every 72 h · subcutaneous · 21 daysAs given in this study (rat).

    Source sentences

    Summary
    suppressed NOD-like receptor pyrin domain-containing protein 3 (NLRP3) inflammasome expression
    1 context sentence
    Summary · context
    One-week post-MI, animals with left ventricular ejection fraction ≤40% were randomized to semaglutide (40 µg/kg subcutaneously every 72 h), colchicine (100 µg/kg intraperitoneally daily), or vehicle for 21 days.
  6. 06AnimalAnimal study (in vivo)Mechanism

    In post-infarction rats with reduced ejection fraction, semaglutide prevented connexin-43 lateralization.

    In plain wordsIn rats with heart damage after a heart attack, semaglutide prevented a harmful shift in the position of a heart cell channel protein.

    Outcome
    DecreaseConnexin-43 lateralization
    Study

    ratn: not reported in source

    Post-myocardial infarction rats with reduced ejection fraction
    Comparator
    Vehicle
    Outcome group
    Heart function · Cardiovascular
    Studied dose
    40 µg/kg every 72 h · subcutaneous · 21 daysAs given in this study (rat).

    Source sentences

    Summary
    prevented connexin-43 (Cx43) lateralization
    1 context sentence
    Summary · context
    One-week post-MI, animals with left ventricular ejection fraction ≤40% were randomized to semaglutide (40 µg/kg subcutaneously every 72 h), colchicine (100 µg/kg intraperitoneally daily), or vehicle for 21 days.
  7. 07AnimalAnimal study (in vivo)Mechanism

    In post-infarction rats with reduced ejection fraction, semaglutide reduced expression of the proarrhythmic SK4 potassium channel.

    In plain wordsIn rats with heart damage after a heart attack, semaglutide lowered a potassium channel protein linked to irregular heartbeat.

    Outcome
    DecreaseSK4 channel expression
    Study

    ratn: not reported in source

    Post-myocardial infarction rats with reduced ejection fraction
    Comparator
    Vehicle
    Outcome group
    Heart function · Cardiovascular
    Studied dose
    40 µg/kg every 72 h · subcutaneous · 21 daysAs given in this study (rat).

    Source sentences

    Summary
    reduced expression of the proarrhythmic small-conductance calcium-activated potassium channel 4 (SK4)
    1 context sentence
    Summary · context
    One-week post-MI, animals with left ventricular ejection fraction ≤40% were randomized to semaglutide (40 µg/kg subcutaneously every 72 h), colchicine (100 µg/kg intraperitoneally daily), or vehicle for 21 days.

AI wrote and checked these results. AI can make mistakes, so check important results against the source.

Version history

PepBank keeps every version of the data on this study. Status changes from Retraction Watch, Europe PMC and Crossref are listed with their source.

  1. Version 2Current

    11 Oct 2026, 00:04 UTC

    Study results updated

  2. Version 1

    9 Oct 2026, 03:06 UTC

    First added · source update from Europe PMC

Subjects

Terms as the source lists them.

PepBank is a research reference. Talk to a doctor before you use any peptide.