# Effect of a Triterpenoid-Rich Olive Oil on Chronic Kidney Disease in an Experimental Model of Diabetes Mellitus

**Authors:** José Pedro De La Cruz, Laura Osuna-Esteban, María Dolores Rodríguez-Pérez, Laura Ortega-Hombrados, Ana María Sánchez-Tévar, Esther Martín-Aurioles, María África Fernández-Prior, Sergio Pérez-Burillo, Juan Antonio Espejo-Calvo, José Antonio González-Correa

PMC · DOI: 10.3390/nu16162794 · Nutrients · 2024-08-21

## TL;DR

This study shows that olive oil rich in triterpenoids can reduce kidney damage in diabetic rats by lowering oxidative stress.

## Contribution

The study demonstrates the protective effect of triterpenoid-rich olive oil on diabetic nephropathy in an experimental model.

## Key findings

- DDOO significantly reduced renal damage and oxidative stress in diabetic rats.
- DDOO was more effective than DOO in preventing kidney damage in diabetic rats.
- Triterpenoids appear to play a key role in reducing diabetic nephropathy.

## Abstract

The aim of this study was to assess the effect of triterpenoids on the development of diabetic nephropathy in an experimental model of diabetes mellitus. For this purpose, a destoned and dehydrated olive oil (DDOO) was used, comparing its effects to a destoned olive oil (DOO). DDOO had a higher triterpenoid content than DOO but an equal content of alcoholic polyphenols. Four study groups (n = 10 animals/group) were formed: healthy rats, diabetic control rats (DRs), and DRs treated orally with 0.5 mL/kg/day of DOO or DDOO for two months. DRs showed impaired renal function (proteinuria, increased serum creatinine, decreased renal creatinine clearance) and morphology (glomerular volume and glomerulosclerosis). These alterations correlated with increased systemic and renal tissue oxidative stress and decreased prostacyclin production. DDOO administration significantly reduced all variables of renal damage, as well as systemic and renal oxidative stress, to a greater extent than the effect produced by DOO. In conclusion, triterpenoid-rich olive oil may prevent kidney damage in experimental diabetes mellitus.

## Linked entities

- **Chemicals:** triterpenoids (PubChem CID 71597391), prostacyclin (PubChem CID 5282411)
- **Diseases:** diabetes mellitus (MONDO:0005015), chronic kidney disease (MONDO:0005300), diabetic nephropathy (MONDO:0005016)
- **Species:** Rattus norvegicus (taxon 10116)

## Full-text entities

- **Diseases:** Diabetes Mellitus (MESH:D003920), proteinuria (MESH:D011507), impaired renal function (MESH:D007674), diabetic nephropathy (MESH:D003928), Chronic Kidney Disease (MESH:D051436), glomerulosclerosis (MESH:D005921)
- **Species:** Rattus norvegicus (brown rat, species) [taxon 10116]

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11357248/full.md

## References

43 references — full list in the complete paper: https://tomesphere.com/paper/PMC11357248/full.md

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Source: https://tomesphere.com/paper/PMC11357248