Eicosapentaenoic acid
From Wikipedia, the free encyclopedia
Eicosapentaenoic acid (EPA or also icosapentaenoic acid) is an omega-3 fatty acid. In physiological literature, it is given the name 20:5(n-3). Its systematic chemical name is all-cis-5,8,11,14,17-icosapentaenoic acid. It also has the trivial name timnodonic acid. Chemically, EPA is a carboxylic acid with a 20-carbon chain and five cis double bonds; the first double bond is located at the third carbon from the omega end. It has the molecular formula C20H30O2.
- EPA and its metabolites act in the body largely by their interactions with the metabolites of arachidonic acid; see Essential fatty acid interactions for detail.
EPA is a polyunsaturated fatty acid that acts as a precursor for prostaglandin-3 (which inhibits platelet aggregation), thromboxane-3 and leukotriene-5 groups. It is found in fish oils of cod liver, herring, mackerel, salmon, menhaden and sardine. It is also found in human breast milk.
The US National Institute of Health's MedlinePlus lists a large number of conditions in which EPA (alone or in concert with other ω-3 sources) is known or thought to be effective. (NIH Medline Plus) Most of these involve its ability to lower inflammation.
[edit] References
- NIH Medline Plus. MedlinePlus Herbs and Supplements: Omega-3 fatty acids, fish oil, alpha-linolenic acid. Retrieved on February 14, 2006.
[edit] See also
- Omega-3 fatty acid
- List of omega-3 fatty acids
- Essential fatty acid
- Eicosanoid
- Fish oilde:Eicosapentaensäure
fr:Acide eicosapentaénoïque sv:EPA (fettsyra)


