# Blueprint of the distinct metabolite profiles of healthy pig heart chambers

**Authors:** Retu Haikonen, Topi Meuronen, Ville Koistinen, Olli Kärkkäinen, Tomi Tuomainen, Gloria I Solano-Aguilar, Joseph F. Urban, Marko Lehtonen, Pasi Tavi, Kati Hanhineva

PMC · DOI: 10.1016/j.jmccpl.2025.100462 · Journal of Molecular and Cellular Cardiology Plus · 2025-06-10

## TL;DR

This study shows that healthy pig heart chambers have distinct metabolic profiles, with the left ventricle showing higher energy demand and oxidative stress.

## Contribution

The study provides the first comprehensive metabolomic characterization of all four heart chambers in a healthy pig model.

## Key findings

- The left ventricle has elevated levels of energy-related metabolites like NAD+ and FAD.
- Ventricles show distinct redox states with variations in glutathione and ascorbic acid.
- Amino acid abundance patterns suggest chamber-specific roles in protein synthesis and repair.

## Abstract

The heart is one of the most studied organs, with physiological processes and disease research. While it is well-established that significant structural and functional differences exist between the chambers, most studies focus on only a single heart chamber, predominantly the left ventricle. This study aims to comprehensively characterise the chamber-specific metabolic profiles of all four heart chambers in a healthy animal model close to human metabolism, pigs. We employed liquid chromatography-mass spectrometry metabolomics to analyse the metabolite profiles of heart chambers in healthy pigs (N = 30) maintained on an ad libitum diet and housed under standard, non-stressed physiological conditions. Our findings reveal a higher energy demand in the left ventricle, as evidenced by elevated levels of electron transport chain-related metabolites such as NAD+ and FAD. Additionally, hexose-phosphates and several acylcarnitines exhibited chamber-dependent variations in abundance. The ventricles, particularly the left, demonstrated distinct redox states, with differential levels of glutathione and ascorbic acid, suggesting variations in oxidative stress across chambers. Furthermore, amino acids had chamber-specific abundance patterns, and ventricles showed an increased requirement for protein synthesis, likely associated with repair mechanisms following reactive oxygen species (ROS)-induced cellular damage. Our study reveals significant differences in the metabolic profiles across four heart chambers in healthy pig hearts, underscoring the metabolic heterogeneity of cardiac tissue. These findings highlight the necessity of investigating chamber-specific metabolic pathways to better understand heart functionality. Such insights could inform the development of more precise therapeutic strategies tailored to metabolic demands and functional roles in heart chambers.

Unlabelled Image

•Significant metabolic differences measured in healthy pig heart chambers.•Left ventricle displays elevated energy demand and oxidative stress markers.•Amino acid patterns reflect chamber-specific metabolic and protein synthesis roles.•Findings underscore metabolic heterogeneity even in the undamaged heart model.

Significant metabolic differences measured in healthy pig heart chambers.

Left ventricle displays elevated energy demand and oxidative stress markers.

Amino acid patterns reflect chamber-specific metabolic and protein synthesis roles.

Findings underscore metabolic heterogeneity even in the undamaged heart model.

## Linked entities

- **Chemicals:** NAD+ (PubChem CID 5892), FAD (PubChem CID 643975), glutathione (PubChem CID 124886), ascorbic acid (PubChem CID 9888239)

## Full-text entities

- **Chemicals:** ascorbic acid (MESH:D001205), amino acids (MESH:D000596), ROS (MESH:D017382), hexose-phosphates (MESH:D006600), FAD (MESH:D005182), NAD+ (MESH:D009243), glutathione (MESH:D005978), acylcarnitines (MESH:C116917)
- **Species:** Sus scrofa (pig, species) [taxon 9823], Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

9 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12221441/full.md

## References

64 references — full list in the complete paper: https://tomesphere.com/paper/PMC12221441/full.md

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Source: https://tomesphere.com/paper/PMC12221441