# Nutritional and Metabolic Consequences of Camelina Seed Oil Compared to Flaxseed Oil in a Rat Diet

**Authors:** Reshma Susan Babu, Adam Jurgoński

PMC · DOI: 10.3390/molecules30132738 · 2025-06-25

## TL;DR

This study compares camelina seed oil and flaxseed oil in rats, finding similar metabolic benefits but potential risks with camelina oil.

## Contribution

The study provides new insights into the metabolic and nutritional effects of camelina seed oil compared to flaxseed oil in a rat model.

## Key findings

- Camelina and flaxseed oils increased lean mass and improved blood lipid profiles compared to palm oil.
- Both oils upregulated the PPARγ gene, suggesting enhanced metabolic regulation.
- Higher liver enzyme activity and lipid peroxidation were observed in rats fed camelina and flaxseed oils.

## Abstract

Camelina seeds are rich in α-linolenic acid (ALA), but also contain small amounts of erucic acid, which is considered toxic to laboratory rats. This experiment compares the dietary inclusion of camelina oil to that of flaxseed oil, a well-known source of ALA, and evaluates their effects on the nutritional and metabolic status of growing rats. The oils were chemically analyzed and incorporated into a semi-purified diet for 4 weeks. The experiment was divided into 3 groups: PO (control-fed palm oil with a trace of ALA), FO (comparative-fed flaxseed oil), and CO (experimental-fed camelina seed oil). Both CO and FO showed a higher percentage of lean body mass, greater lean mass gain, and a lower fat percentage compared to PO. Similar to the body composition, the blood lipid profile also improved in CO and FO, with higher HDL cholesterol and lower triglyceride levels, which was associated with upregulation of the peroxisome proliferator-activated receptor γ gene. However, in FO and CO, higher plasma liver enzyme activity and malondialdehyde concentrations were observed in the heart and liver. The results suggest that camelina oil has a similarly beneficial impact on the metabolic processes of the growing body as flaxseed oil, while also indicating a potential for increased organ-specific lipid peroxidation and hepatic burden when consumed in excess.

## Linked entities

- **Genes:** PPARG (peroxisome proliferator activated receptor gamma) [NCBI Gene 5468]
- **Chemicals:** α-linolenic acid (PubChem CID 5280934), erucic acid (PubChem CID 5281116), malondialdehyde (PubChem CID 10964)
- **Species:** Rattus norvegicus (taxon 10116)

## Full-text entities

- **Genes:** Pparg (peroxisome proliferator-activated receptor gamma) [NCBI Gene 25664] {aka PPARgamma2}
- **Chemicals:** palm oil (MESH:D000073878), triglyceride (MESH:D014280), lipid (MESH:D008055), FO (MESH:D008043), ALA (MESH:D017962), malondialdehyde (MESH:D008315), erucic acid (MESH:C049811), PO (MESH:D011059), CO (-), oils (MESH:D009821)
- **Species:** Rattus norvegicus (brown rat, species) [taxon 10116], Camelina (genus) [taxon 71323]

## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12250771/full.md

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Source: https://tomesphere.com/paper/PMC12250771