Polyunsaturated fatty acids and their metabolites in brain function and disease

被引:0
作者
Richard P. Bazinet
Sophie Layé
机构
[1] University of Toronto,Department of Nutritional Sciences
[2] INRA,undefined
[3] Nutrition et Neurobiologie Intégrée,undefined
[4] UMR 1286,undefined
[5] University of Bordeaux,undefined
[6] Nutrition et Neurobiologie Intégrée,undefined
[7] UMR 1286,undefined
来源
Nature Reviews Neuroscience | 2014年 / 15卷
关键词
D O I
暂无
中图分类号
学科分类号
摘要
The brain is especially enriched with the two polyunsaturated fatty acids arachidonic acid and docosahexaenoic acid. Although, quantitatively speaking, they are primarily esterified to brain phophospholipids, they can be released from the membrane and transformed into highly biologically active molecules.The mechanisms by which the brain takes up polyunsaturated fatty acids are not clear and remain controversial. Candidate plasma pools include phospholipids as part of lipoproteins, unesterified fatty acids and lysophospholipids. Because polyunsaturated fatty acids are derived from the diet, changes in their intakes can alter brain levels and thus the activity of pathways regulated by polyunsaturated fatty acids in the brain.In response to neuroreceptor activation, fatty acids are released from the membrane and participate in cell signalling.So far, polyunsaturated fatty acids and their biologically active derivatives have been shown to regulate cell survival, neurogenesis, brain inflammation and synaptic function.Altered fatty acid signalling has been implicated in mood disorders, cognition, Alzheimer's disease, schizophrenia and other conditions. Research using animal models has shown promise in targeting brain polyunsaturated fatty acid metabolism with diet or drugs; however, translational studies often do not yield statistically significant results. New methods to target brain polyunsaturated metabolism are emerging as novel approaches to treat brain disorders.
引用
收藏
页码:771 / 785
页数:14
相关论文
共 447 条
[31]  
Lauritzen L(2002)The emerging role of group VI calcium-independent phospholipase A2 in releasing docosahexaenoic acid from brain phospholipids Neurochem. Res. 27 1641-1647
[32]  
Carlson SE(1995)Energy consumption by phospholipid metabolism in mammalian brain J. Neurochem. 64 2765-2772
[33]  
Makrides M(1991)Dopamine D2 receptors potentiate arachidonate release via activation of cytosolic, arachidonate-specific phospholipase A2 Proc. Natl Acad. Sci. USA 88 6477-6480
[34]  
Anderson A(1990)A transduction pathway associated with receptors coupled to the inhibitory guanine nucleotide binding protein Gi that amplifies ATP-mediated arachidonic acid release Proc. Natl Acad. Sci. USA 87 2187-2191
[35]  
Gibson RA(1988)Serotonin stimulates phospholipase A2 and the release of arachidonic acid in hippocampal neurons by a type 2 serotonin receptor that is independent of inositolphospholipid hydrolysis Nature 336 68-70
[36]  
Collins CT(1990)NMDA receptors activate the arachidonic acid cascade system in striatal neurons Biochem. Soc. Trans. 18 503-507
[37]  
Carver JD(2014)Receptor-mediated activation of phospholipase A2 and arachidonic acid release in signal transduction ACS Chem. Neurosci. 5 459-467
[38]  
Benford VJ(2011)Lithium and the other mood stabilizers effective in bipolar disorder target the rat brain arachidonic acid cascade Annu. Rev. Nutr. 31 321-351
[39]  
Han B(2012)Docosahexaenoic acid signalolipidomics in nutrition: significance in aging, neuroinflammation, macular degeneration, Alzheimer's, and other neurodegenerative diseases Brain Res. Bull. 87 154-171
[40]  
Cantor AB(2010)Imaging brain signal transduction and metabolism via arachidonic and docosahexaenoic acid in animals and humans Prostaglandins Other Lipid Mediators 91 63-67