| Literature DB >> 19770016 |
Géraldine Mathieu1, Mathieu Géraldine, Stéphanie Denis, Denis Stéphanie, Bénédicte Langelier, Langelier Bénédicte, Isabelle Denis, Denis Isabelle, Monique Lavialle, Lavialle Monique, Sylvie Vancassel, Vancassel Sylvie.
Abstract
Polyunsaturated fatty acids (PUFAs), particularly docosahexaenoic acid (DHA) and arachidonic acid (AA), are the main components of the phospholipids, in cerebral membranes. A dietary-induced cerebral DHA deficit results in altered behaviour and neurotransmission in rodents. To determine whether PUFA were acting on the neurotransmitter release machinery, we measured the release of [(3)H]-noradrenaline (NA) from SH-SY5Y neuroblastoma cells with modified PUFA membrane contents and from cells incubated with medium containing high DHA or AA. The membranes of cells incubated with 70 microM DHA for 3 days had 7.6-times more DHA in their ethanolamine glycerophospholipids, while the membranes of cells incubated with AA had 40% less. Incorporation of DHA enhanced basal [(3)H]-NA release (25%, p<0.05), but not KCl-evoked [(3)H]-NA release. Brief incubation with DHA during vesicle mobilization also strongly increased [3H]-NA release. AA had no effect. The genes encoding for the calcium sensor synaptotagmin 1, and for the two SNARE complex proteins syntaxin 1A and synaptobrevin 1 were not affected by PUFA incorporation, as indicated by assays for specific mRNAs and proteins. Thus both a high membrane DHA content and free DHA in the medium enhance the release of [(3)H]-NA from SH-SY5Y cells. This suggests that brain membrane DHA influences exocytosis, which then regulates neurotransmission. 2009 Elsevier Ltd. All rights reserved.Entities:
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Year: 2009 PMID: 19770016 DOI: 10.1016/j.neuint.2009.09.006
Source DB: PubMed Journal: Neurochem Int ISSN: 0197-0186 Impact factor: 3.921