Evidence map›Paper›PMID 42485931›Full record

ArticleJACC. Basic to translational science2026

The Orally Available Ghrelin Receptor-Agonist AC01 Improves Systolic Function in HFrEF Mice and Nonhuman Primates.

Lars H Lund, Camilla Hage, Mattias Carlström, Pascal Champéroux, Marcus Ståhlberg, Patrik Strömberg, Göran Westerberg, Emanuela Lovati, Allan Gordon, Johan Sjödahl and 2 more

Abstract read
In one paragraph

Article in JACC. Basic to translational science, 2026. 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

12 authors.

Lars H LundDepartment of Medicine, Cardiology Unit, Karolinska Institutet, Stockholm, Sweden; Department of Cardiology, Heart and Vascular Center, Karolinska University Hospital, Stockholm, Sweden. Electronic address: lars.lund@ki.se.
Camilla HageDepartment of Medicine, Cardiology Unit, Karolinska Institutet, Stockholm, Sweden; Department of Cardiology, Heart and Vascular Center, Karolinska University Hospital, Stockholm, Sweden.
Mattias CarlströmDepartment of Physiology and Pharmacology, Karolinska Institutet, Stockholm, Sweden.
Pascal ChampérouxEuropean Research Biology Center (ERBC) France, Baugy, France.
Marcus StåhlbergDepartment of Medicine, Cardiology Unit, Karolinska Institutet, Stockholm, Sweden; Department of Cardiology, Heart and Vascular Center, Karolinska University Hospital, Stockholm, Sweden.
Patrik StrömbergAnaCardio AB, Stockholm, Sweden.
Göran WesterbergAnaCardio AB, Stockholm, Sweden.
Emanuela LovatiHelsinn Healthcare SA, Lugano, Switzerland.
Allan GordonAnaCardio AB, Stockholm, Sweden.
Johan SjödahlAnaCardio AB, Stockholm, Sweden.
Daniel C AnderssonDepartment of Cardiology, Heart and Vascular Center, Karolinska University Hospital, Stockholm, Sweden; Department of Physiology and Pharmacology, Karolinska Institutet, Stockholm, Sweden.
Gianluigi PirontiDepartment of Medicine, Cardiology Unit, Karolinska Institutet, Stockholm, Sweden; Department of Physiology and Pharmacology, Karolinska Institutet, Stockholm, Sweden. Electronic address: gianluigi.pironti@ki.se.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Heart failure with reduced ejection fraction (HFrEF) is characterized by impaired cardiac contractility. AC01, a small-molecule ghrelin receptor agonist, enhances contractility in cardiomyocytes. This study evaluated the in vivo hemodynamic effects of AC01 in a mouse HFrEF model and in cynomolgus monkeys. In HFrEF mice, intravenous AC01 significantly increased cardiac output, stroke volume, and ejection fraction versus vehicle, without any apparent detriment to diastolic function. Pressure-volume loop analysis demonstrated load-independent inotropic effects. In monkeys, oral AC01 increased cardiac output and stroke volume while reducing heart rate, without lowering central aortic pressure. These effects were sustained over 14 days of oral dosing. Additionally, AC01 improved autonomic balance by increasing parasympathetic and decreasing sympathetic activity. Overall, AC01 produced rapid, consistent, and sustained improvements in systolic function across species, supporting its potential as a novel, load-independent inotropic therapy for heart failure.

Indexed as

AC01contractilityghrelin receptor agonisthemodynamicsHFrEFinotrope

Identifiers

PMID42485931
PMCPMC13416467

What OpenQuestion holds

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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.