# Cardioprotective Peptides from Dry-Cured Ham in Primary Endothelial Cells and Human Plasma: An Omics Approach

**Authors:** Clara Noguera-Navarro, Javier Stelling, Esteban Orenes-Piñero, Caterina Pipino, Francisco José Nicolás, Silvia Montoro-García

PMC · DOI: 10.3390/antiox14070772 · Antioxidants · 2025-06-24

## TL;DR

This study explores how bioactive peptides from dry-cured ham protect heart health by reducing inflammation and oxidative stress in endothelial cells and human plasma.

## Contribution

The study introduces a novel integrative omics approach to evaluate the cardioprotective effects of peptides from dry-cured ham.

## Key findings

- BP treatment altered mitochondrial gene expression and reduced inflammation and oxidative stress in healthy HUVECs.
- BP modulated key signaling pathways like Ras and MAPK, affecting ERK, AKT, and NF-κB phosphorylation.
- In human plasma, BP modulated lipid metabolism and inflammation, with changes in proteins like APOA1 and MMP-8.

## Abstract

Cardiovascular diseases are a leading cause of mortality, driving the search for alternative preventive strategies. This study investigates the antioxidant effects, among others, of a mixture of four bioactive peptides (BPs) derived from dry-cured pork ham on endothelial cells from healthy (C-HUVECs) and gestational diabetes (GD-HUVECs) pregnancies, as well as human plasma, using an integrative omics approach. Human umbilical vein endothelial cells (HUVECs) were treated with 300 μM purified BP, followed by transcriptomic and proteomic analyses. The results revealed significant alterations in mitochondrial gene expression and downregulation of genes associated with inflammation and oxidative stress in healthy HUVECs. Furthermore, BP treatment modulated key signalling pathways, including Ras and MAPK, leading to changes in the phosphorylation of ERK, AKT, and NF-κB, suggesting potential cardioprotective effects. The effects of BP were compared to those of the antioxidant hydroxytyrosol, highlighting their relative efficacy in vascular protection. The proteomic analysis of human plasma demonstrated BP-induced modulation of lipid metabolism, inflammation, and oxidative stress with notable changes in proteins such as APOA1 and MMP-8. These natural compounds demonstrate significant preventive potential in vascular health, highlighting their promise as effective tools for reducing cardiovascular risk before the progression of the pathology. These findings emphasize the importance of integrative omics in understanding the mechanisms behind BP’s effects and suggest promising applications for nutraceuticals aimed at cardiovascular protection.

## Linked entities

- **Genes:** APOA1 (apolipoprotein A1) [NCBI Gene 335], MMP8 (matrix metallopeptidase 8) [NCBI Gene 4317]
- **Proteins:** EPHB2 (EPH receptor B2), AKT1 (AKT serine/threonine kinase 1), NFKB1 (nuclear factor kappa B subunit 1), APOA1 (apolipoprotein A1), MMP8 (matrix metallopeptidase 8)
- **Chemicals:** hydroxytyrosol (PubChem CID 82755)
- **Diseases:** gestational diabetes (MONDO:0005406)
- **Species:** Homo sapiens (taxon 9606)

## Full-text entities

- **Genes:** AKT1 (AKT serine/threonine kinase 1) [NCBI Gene 207] {aka AKT, PKB, PKB-ALPHA, PRKBA, RAC, RAC-ALPHA}, MMP8 (matrix metallopeptidase 8) [NCBI Gene 4317] {aka CLG1, HNC, MMP-8, PMNL-CL}, NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790] {aka CVID12, EBP-1, KBF1, NF-kB, NF-kB1, NF-kappa-B1}, APOA1 (apolipoprotein A1) [NCBI Gene 335] {aka AMYLD3, HPALP2, apo(a)}, MAPK1 (mitogen-activated protein kinase 1) [NCBI Gene 5594] {aka ERK, ERK-2, ERK2, ERT1, MAPK2, NS13}
- **Diseases:** Cardiovascular diseases (MESH:D002318), gestational diabetes (MESH:D016640), inflammation (MESH:D007249)
- **Chemicals:** hydroxytyrosol (MESH:C005975), lipid (MESH:D008055), BP (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12291938/full.md

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12291938/full.md

## References

62 references — full list in the complete paper: https://tomesphere.com/paper/PMC12291938/full.md

---
Source: https://tomesphere.com/paper/PMC12291938