# Growth Hormone-Releasing Peptide-6 (GHRP-6) Ameliorates Post-Infarct Ventricular Remodeling and Systolic Dysfunction in a Model of Permanent Coronary Ligation

**Authors:** Linlin Wang, Arielis Rodriguez-Ulloa, Jorge Berlanga-Acosta, Ariana García-Ojalvo, Angel Abreu-Cruz, Luis Javier Gonzalez-López, Vladimir Besada-López, Yassel Ramos-Gómez, Gerardo Guillén-Nieto, Baohong Jiang

PMC · DOI: 10.3390/ph19030468 · Pharmaceuticals · 2026-03-12

## TL;DR

GHRP-6, a growth hormone-releasing peptide, reduces heart damage and improves heart function after a heart attack in rats.

## Contribution

GHRP-6 is shown to reduce myocardial scarring and improve heart function through specific molecular pathways.

## Key findings

- GHRP-6 reduced myocardial tissue demise and interstitial fibrosis.
- GHRP-6 improved left ventricle physiology in infarcted rats.
- Proteomic analysis suggests GHRP-6 activates fatty acid oxidation and antioxidant pathways.

## Abstract

Background/Objective: GHRP-6 is a GH secretagogue hexapeptide with expanding and promising cardioprotective effects. Having determined 0.4 mg/kg as the minimum effective dose for enhancing inotropy based on echocardiographic parameters in healthy rats, we implemented a non-reperfusion myocardial infarct model, with its consequent left ventricle wall thinning and ballooning, via permanent left descending coronary artery ligation. Methods: Rats were assigned to three groups: sham-operated/normal rats, infarcted + saline-treated control rats, and infarcted + GHRP-6-administration rats. Treatments were initiated post-surgery and continued for 7 days. On day 7, the animals were echocardiographically and histologically evaluated. For mitochondrial proteomic analysis, an additional 12 healthy rats were used. Six animals received GHRP-6 or normal saline and were observed for 6 h after the inoculation. Results: Here, we show that GHRP-6 attenuated myocardial tissue demise, reduced myocardial interstitial fibrosis/scarring, and integrally improved left ventricle physiology. The proteomic analysis indicated that the GHRP-6 cardioprotective effects may be theoretically mediated by the concerted upregulation of proteins/pathways involved in fatty acid beta-oxidation, apoptosis prevention pathways, antioxidant defenses, and mitochondrial metabolic reprogramming. Conclusions: GHRP-6 is a potent cardioprotective candidate attenuating morphological and functional outcomes caused by late ischemia.

## Linked entities

- **Chemicals:** GHRP-6 (PubChem CID 4345065)
- **Diseases:** myocardial infarct (MONDO:0005068)
- **Species:** Rattus norvegicus (taxon 10116)

## Full-text entities

- **Genes:** Ggh (gamma-glutamyl hydrolase) [NCBI Gene 25455]
- **Diseases:** ischemia (MESH:D007511), Post-Infarct (MESH:D007238), Systolic Dysfunction (MESH:D006331), Ventricular Remodeling (MESH:D020257), myocardial infarct (MESH:D009203), fibrosis (MESH:D005355)
- **Chemicals:** fatty acid (MESH:D005227)
- **Species:** Rattus norvegicus (brown rat, species) [taxon 10116]

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13029777/full.md

## References

70 references — full list in the complete paper: https://tomesphere.com/paper/PMC13029777/full.md

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Source: https://tomesphere.com/paper/PMC13029777