# Pequi (Caryocar brasiliense, Camb) Bark Extract Reduces ROS Production in Diabetic Human Coronary Endothelial Cells

**Authors:** Karla M. S. Braga, Eugenio G. Araujo, Frank W. Sellke, M. Ruhul Abid

PMC · DOI: 10.3390/antiox14101167 · Antioxidants · 2025-09-25

## TL;DR

Pequi bark extract reduces harmful oxygen molecules in diabetic heart cells, potentially improving heart health in people with Type 2 diabetes.

## Contribution

The study shows pequi extract reduces ROS and boosts antioxidant enzymes in diabetic endothelial cells.

## Key findings

- Pequi extract reduced cytosolic and mitochondrial ROS in diabetic cells under stress conditions.
- It upregulated antioxidant enzymes like Nrf2, HO-1, and SOD through the Nrf2 pathway.
- The extract enhanced cell proliferation in diabetic coronary endothelial cells.

## Abstract

Reactive oxygen species (ROS) overproduction contributes to endothelial dysfunction in Type 2 diabetes mellitus (T2DM). Pequi (Caryocar brasiliense, Camb), a native Brazilian fruit, is rich in polyphenolic antioxidants. We investigated whether its ethanolic bark extract modulates ROS levels and promotes proliferation in human coronary artery endothelial cells from patients with diabetes (D-HCAECs). Cells were treated with pequi extract under normoxic, hypoxic, or H2O2-induced oxidative stress conditions. Cytosolic and mitochondrial ROS levels, cell proliferation, and the expression of antioxidant proteins (Nrf2, HO-1, SOD1, SOD2, catalase, and GPx1) were assessed. Pequi significantly reduced cytosolic ROS under normoxia and both cytosolic and mitochondrial ROS under stress. It also upregulated antioxidant enzymes through the Nrf2 pathway and enhanced D-HCAEC proliferation under all tested conditions. These results suggest that pequi’s antioxidant effects may be mediated by the increased expression of endogenous enzymes, leading to improved redox balance and endothelial function in diabetic coronary vasculature.

## Linked entities

- **Genes:** GABPA (GA binding protein transcription factor subunit alpha) [NCBI Gene 2551], HMOX1 (heme oxygenase 1) [NCBI Gene 3162], SOD1 (superoxide dismutase 1) [NCBI Gene 6647], SOD2 (superoxide dismutase 2) [NCBI Gene 6648], GPX1 (glutathione peroxidase 1) [NCBI Gene 2876]
- **Proteins:** GABPA (GA binding protein transcription factor subunit alpha), HMOX1 (heme oxygenase 1), SOD1 (superoxide dismutase 1), SOD2 (superoxide dismutase 2), Cat (Catalase), GPX1 (glutathione peroxidase 1)
- **Chemicals:** H2O2 (PubChem CID 784)
- **Diseases:** Type 2 diabetes mellitus (MONDO:0005148)
- **Species:** Homo sapiens (taxon 9606)

## Full-text entities

- **Genes:** CAT (catalase) [NCBI Gene 847], GPX1 (glutathione peroxidase 1) [NCBI Gene 2876] {aka GPXD, GSHPX1}, SOD1 (superoxide dismutase 1) [NCBI Gene 6647] {aka ALS, ALS1, HEL-S-44, IPOA, SOD, STAHP}, NFE2L2 (NFE2 like bZIP transcription factor 2) [NCBI Gene 4780] {aka IMDDHH, NRF2, Nrf-2}, SOD2 (superoxide dismutase 2) [NCBI Gene 6648] {aka GC1, GClnc1, IPO-B, IPOB, MNSOD, MVCD6}, HMOX1 (heme oxygenase 1) [NCBI Gene 3162] {aka HMOX1D, HO-1, HSP32, bK286B10}
- **Diseases:** Diabetic (MESH:D003920), T2DM (MESH:D003924)
- **Chemicals:** ROS (MESH:D017382), Bark (-), H2O2 (MESH:D006861)
- **Species:** Homo sapiens (human, species) [taxon 9606], Caryocar brasiliense (species) [taxon 480971]
- **Cell lines:** D-HCAEC — Drosophila melanogaster (Fruit fly), Spontaneously immortalized cell line (CVCL_IZ09)

## Full text

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## Figures

10 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12562227/full.md

## References

33 references — full list in the complete paper: https://tomesphere.com/paper/PMC12562227/full.md

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Source: https://tomesphere.com/paper/PMC12562227