2014
DOI: 10.1038/nrn3820
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Polyunsaturated fatty acids and their metabolites in brain function and disease

Abstract: The brain is highly enriched with fatty acids. These include the polyunsaturated fatty acids (PUFAs) arachidonic acid and docosahexaenoic acid, which are largely esterified to the phospholipid cell membrane. Once PUFAs are released from the membrane, they can participate in signal transduction, either directly or after enzymatic conversion to a variety of bioactive derivatives ('mediators'). PUFAs and their mediators regulate several processes within the brain, such as neurotransmission, cell survival and neur… Show more

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Cited by 1,080 publications
(918 citation statements)
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References 196 publications
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“…In addition, while DHA is the most abundant fatty acid in the brain, EPA only represents ≤1% of total brain fatty acids (Bos et al 2016). In addition, although EPA can be transformed into DHA, evidence suggests EPA is rapidly and extensively ß-oxidized (generating acetyl-CoA) upon entry into the brain (Bazinet and Laye 2014;Chen and Bazinet 2015). Because this process results in little to no extra EPA available in the brain, and the ß-oxidized products are not specific for EPA, this suggests that EPA's efficacy cannot be explained by an effect in the brain, and that EPA is not only a precursor of DHA but that DHA and EPA have distinct roles.…”
Section: Weighing the Evidencementioning
confidence: 99%
“…In addition, while DHA is the most abundant fatty acid in the brain, EPA only represents ≤1% of total brain fatty acids (Bos et al 2016). In addition, although EPA can be transformed into DHA, evidence suggests EPA is rapidly and extensively ß-oxidized (generating acetyl-CoA) upon entry into the brain (Bazinet and Laye 2014;Chen and Bazinet 2015). Because this process results in little to no extra EPA available in the brain, and the ß-oxidized products are not specific for EPA, this suggests that EPA's efficacy cannot be explained by an effect in the brain, and that EPA is not only a precursor of DHA but that DHA and EPA have distinct roles.…”
Section: Weighing the Evidencementioning
confidence: 99%
“…Therefore, the cellular concentrations of LC n-3 and n-6 PUFA, and their relative derived bioactive products are determined by their relative dietary intake. Increased dietary intake of LC n-3 PUFA has been shown to significantly alter DHA levels in the brain (Freund Levi et al, 2014) suggesting that DHA and EPA dietary supplementation could be used to directly influence neuroinflammatory pathways (Bazinet and Laye, 2014). DHA entry in the brain is still a matter of debate.…”
Section: N-pufas Neuroinflammation and Cognitive Disordersmentioning
confidence: 99%
“…In particular EPA, DHA and their bioactive mediators have potent antiinflammatory and pro-resolving properties in the periphery D103, page 3 of 10 Dossier Q. Leyrolle et al: OCL 2016, 23(1) D103 (Serhan and Chiang, 2013) and in the brain (Bazinet and Laye, 2014;Laye, 2010;Orr and Bazinet, 2008;Rapoport, 2008). Loss of these regulatory processes can result in excessive, inappropriate or on-going inflammation that can cause irreparable damage to host tissues, including the brain.…”
Section: N-pufas Neuroinflammation and Cognitive Disordersmentioning
confidence: 99%
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