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Updated: May 21, 2026

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A Clinical Trial Assessing the Safety, Efficacy, and Delivery of Olive-Oil-Based Three-Chamber Bags for Parenteral Nutrition
Published on: September 20, 2019
A short-term n-3 DPA supplementation study in humans
Eliza Miller1, Gunveen Kaur, Amy Larsen
1School of Exercise and Nutrition Sciences, Deakin University, Burwood, VIC, 3126, Australia.
European Journal of Nutrition
|June 26, 2012
Summary
Docosapentaenoic acid (DPA) and eicosapentaenoic acid (EPA) show distinct incorporation patterns into human plasma lipids. DPA supplementation increased DPA, EPA, and docosahexaenoic acid (DHA) levels, suggesting DPA may serve as a reservoir for LC n-3 PUFA.
Area of Science:
- Biochemistry
- Human Nutrition
- Omega-3 Fatty Acids
Background:
- Limited understanding of docosapentaenoic acid (DPA) metabolism compared to EPA and DHA.
- Plasma lipids and red blood cells (RBC) are key sites for fatty acid incorporation.
Purpose of the Study:
- To investigate the uptake and incorporation of pure DPA and EPA into human plasma and RBC lipids.
- To compare the distinct incorporation patterns of DPA and EPA.
Main Methods:
- Ten female participants received 8g of pure DPA or EPA in a randomized crossover, double-blinded manner over 7 days.
- Placebo treatment involved olive oil.
- Blood samples were collected on days 0, 4, and 7 for plasma and RBC fatty acid analysis.
Main Results:
- DPA supplementation increased DPA in plasma phospholipids and triacylglycerols, and also increased EPA and DHA in plasma lipids.
- EPA supplementation increased EPA in plasma cholesterol esters and phospholipids, and in RBC phospholipids.
- Neither DPA nor EPA supplementation altered the proportions of the other fatty acids in RBC phospholipids, indicating specific incorporation patterns.
Conclusions:
- Short-term DPA supplementation leads to distinct incorporation patterns in human plasma lipids.
- DPA may function as a reservoir for major long-chain n-3 polyunsaturated fatty acids (LC n-3 PUFA) in humans.

