Volume 21, Issue 4 , Pages 268-277, April 2010
Effects of eicosapentaenoic acid on synaptic plasticity, fatty acid profile and phosphoinositide 3-kinase signaling in rat hippocampus and differentiated PC12 cells
Abstract
Placebo-controlled clinical studies suggest that intake of n-3 polyunsaturated fatty acids improves neurological disorders such as Alzheimer's disease, Huntington's disease and schizophrenia. To evaluate the impact of eicosapentaenoic acid (EPA), we orally administered highly purified ethyl EPA (EPA-E) to rats at a dose of 1.0 mg/g per day and measured long-term potentiation of the CA1 hippocampal region, a physiological correlate of synaptic plasticity that is thought to underlie learning and memory. The mean field excitatory postsynaptic potential slope of the EPA-E group was significantly greater than that of the control group in the CA1 region. Gene expression of hippocampal p85α, one of the regulatory subunits of phosphatidylinositol 3-kinase (PI3-kinase), was increased with EPA-E administration. Investigation of fatty acid profiles of neuronal and glia-enriched fractions demonstrated that a single administration of EPA-E significantly increased neuronal and glial EPA content and glial docosahexaenoic acid content, clearly suggesting that EPA was indeed taken up by both neurons and glial cells. In addition, we investigated the direct effects of EPA on the PI3-kinase/Akt pathway in differentiated PC12 cells. Phosphorylated-Akt expression was significantly increased in EPA-treated cells, and nerve growth factor withdrawal-induced increases in cell death and caspase-3 activity were suppressed by EPA treatment. These findings suggest that EPA protects against neurodegeneration by modulating synaptic plasticity and activating the PI3-kinase/Akt pathway, possibly by its own functional effects in neurons and glial cells and by its capacity to increase brain docosahexaenoic acid.
Abbreviations: AA, arachidonic acid, Abeta, amyloid-beta peptide, AD, Alzheimer's disease, ALA, α-linolenic acid, APP, beta-amyloid precursor protein, ATP, adenosine 5′-triphosphate, CNS, central nervous system, CREB, cyclic AMP response element-binding protein, DAPI, 4′,6-diamidino-2-phenylindole, DG, dentate gyrus, DHA, docosahexaenoic acid, DMEM, Dulbecco's Modified Eagle's Medium, DPA, docosapentaenoic acid, DPBS, Dulbecco's phosphate-buffered saline, EPA, eicosapentaenoic acid, EPA-E, ethyl EPA, FAMEs, fatty acid methyl esters, fEPSPs, field excitatory postsynaptic potentials, GAPDH, glyceraldehyde-3-phosphate dehydrogenase, GFAP, glial fibrillary acidic protein, LTP, long-term potentiation, NGF, nerve growth factor, n-3 PUFAs, n-3 polyunsaturated fatty acids, PG, prostaglandin, PI3-kinase, phosphatidylinositol 3-kinase, PLA2, phospholipase A2, RT-PCR, reverse transcription-polymerase chain reaction, TBS, theta burst conditioning stimulation
Keywords: Eicosapentaenoic acid, Brain, n-3 fatty acids, Phosphatidylinositol 3-kinase, Long-term potentiation, Neuron
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PII: S0955-2863(09)00004-7
doi:10.1016/j.jnutbio.2008.12.015
© 2010 Elsevier Inc. All rights reserved.
Volume 21, Issue 4 , Pages 268-277, April 2010
