Cited by 167

The DOI matches its Crossref record; 40 of the 40 references it cites were found in a registry or an index.

Fatty acid metabolism in the progression and resolution of CNS disorders

Bogie, Jeroen F.J., Haidar, Mansour, Kooij, Gijs, Hendriks, Jerome J.A.·2020·Advanced Drug Delivery Reviews

Abstract

Recent advances in lipidomics and metabolomics have unveiled the complexity of fatty acid metabolism and the fatty acid lipidome in health and disease. A growing body of evidence indicates that imbalances in the metabolism and level of fatty acids drive the initiation and progression of central nervous system (CNS) disorders such as multiple sclerosis, Alzheimer's disease, and Parkinson's disease. Here, we provide an in-depth overview on the impact of the β-oxidation, synthesis, desaturation, elongation, and peroxidation of fatty acids on the pathophysiology of these and other neurological disorders. Furthermore, we discuss the impact of individual fatty acids species, acquired through the diet or endogenously synthesized in mammals, on neuroinflammation, neurodegeneration, and CNS repair. The findings discussed in this review highlight the therapeutic potential of modulators of fatty acid metabolism and the fatty acid lipidome in CNS disorders, and underscore the diagnostic value of lipidome signatures in these diseases.

Overview

Integrity signals

Registry

Crossref · 10.1016/j.addr.2020.01.004

Cites

40 of 40 references verified0 citation errors · 0 not checkable

Statistics

Recomputing p-values needs the paper’s full text.

Verification

Claims the paper makes

This paper’s full text isn’t openly available, so its claims and self-check weren’t run. The registry and citation checks still apply.

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

Citations

Cites

Flagged first, then by citations

Show all 40 references

Research works printed but not linked: 253

  1. O'Neill, 2016, A guide to immunometabolism for immunologists, Nature reviews. Immunology, 16, 553, 10.1038/nri.2016.70 · DOI · Paper page
  2. Liu, 2018, Enhanced glycolysis contributes to the pathogenesis of experimental autoimmune neuritis, Journal of neuroinflammation, 15, 10.1186/s12974-018-1095-7 · DOI
  3. Li, 2018, Hexokinase 2-dependent hyperglycolysis driving microglial activation contributes to ischemic brain injury, J Neurochem, 144, 186, 10.1111/jnc.14267 · DOI
  4. Pan, 2019, Sodium rutin ameliorates Alzheimer's disease-like pathology by enhancing microglial amyloid-beta clearance, Sci Adv, 5, 10.1126/sciadv.aau6328 · DOI
  5. Shriver, 2011, Inhibition of fatty acid metabolism ameliorates disease activity in an animal model of multiple sclerosis, Sci Rep, 1, 10.1038/srep00079 · DOI
  6. Samudio, 2010, Pharmacologic inhibition of fatty acid oxidation sensitizes human leukemia cells to apoptosis induction, The Journal of clinical investigation, 120, 142, 10.1172/JCI38942 · DOI
  7. Pike, 2011, Inhibition of fatty acid oxidation by etomoxir impairs NADPH production and increases reactive oxygen species resulting in ATP depletion and cell death in human glioblastoma cells, Biochimica et biophysica acta, 1807, 726, 10.1016/j.bbabio.2010.10.022 · DOI
  8. Ebert, 2003, Energy contribution of octanoate to intact rat brain metabolism measured by 13C nuclear magnetic resonance spectroscopy, The Journal of neuroscience : the official journal of the Society for Neuroscience, 23, 5928, 10.1523/JNEUROSCI.23-13-05928.2003 · DOI · Paper page
  9. Mitchell, 2011, Fatty acid transport into the brain: of fatty acid fables and lipid tails, Prostaglandins Leukot Essent Fatty Acids, 85, 293, 10.1016/j.plefa.2011.04.007 · DOI
  10. Knobloch, 2017, A fatty acid oxidation-dependent metabolic shift regulates adult neural stem cell activity, Cell reports, 20, 2144, 10.1016/j.celrep.2017.08.029 · DOI
  11. Singh, 2013, Histone deacetylase inhibitor upregulates peroxisomal fatty acid oxidation and inhibits apoptotic cell death in abcd1-deficient glial cells, PloS one, 8
  12. Viader, 2013, Aberrant Schwann cell lipid metabolism linked to mitochondrial deficits leads to axon degeneration and neuropathy, Neuron, 77, 886, 10.1016/j.neuron.2013.01.012 · DOI
  13. Yao, 2018, Identifying off-target effects of etomoxir reveals that carnitine palmitoyltransferase I is essential for cancer cell proliferation independent of beta-oxidation, PLoS Biol, 16, 10.1371/journal.pbio.2003782 · DOI
  14. Feingold, 2012, Mechanisms of triglyceride accumulation in activated macrophages, Journal of leukocyte biology, 92, 829, 10.1189/jlb.1111537 · DOI
  15. Cader, 2016, C13orf31 (FAMIN) is a central regulator of immunometabolic function, Nature immunology, 17, 1046, 10.1038/ni.3532 · DOI
  16. Wei, 2016, Fatty acid synthesis configures the plasma membrane for inflammation in diabetes, Nature, 539, 294, 10.1038/nature20117 · DOI
  17. Carroll, 2018, An unexpected link between fatty acid synthase and cholesterol synthesis in proinflammatory macrophage activation, The Journal of biological chemistry, 293, 5509, 10.1074/jbc.RA118.001921 · DOI
  18. Berod, 2014, De novo fatty acid synthesis controls the fate between regulatory T and T helper 17 cells, Nature medicine, 20, 1327, 10.1038/nm.3704 · DOI · Paper page
  19. Cluxton, 2019, Differential regulation of human treg and Th17 cells by fatty acid synthesis and glycolysis, Frontiers in immunology, 10, 115, 10.3389/fimmu.2019.00115 · DOI
  20. Young, 2017, Fatty acid synthase regulates the pathogenicity of Th17 cells, Journal of leukocyte biology, 102, 1229, 10.1189/jlb.3AB0417-159RR · DOI
  21. Wang, 2019, ACC1 (acetyl coenzyme A carboxylase 1) is a potential immune modulatory target of cerebral ischemic stroke, Stroke; a journal of cerebral circulation, 50, 1869, 10.1161/STROKEAHA.119.024564 · DOI
  22. Laplante, 2010, mTORC1 activates SREBP-1c and uncouples lipogenesis from gluconeogenesis, Proceedings of the National Academy of Sciences of the United States of America, 107, 3281, 10.1073/pnas.1000323107 · DOI
  23. Talboom, 2015, The mammalian target of rapamycin at the crossroad between cognitive aging and Alzheimer's disease, NPJ Aging Mech Dis, 1, 10.1038/npjamd.2015.8 · DOI
  24. Liu, 2017, Rapamycin suppresses Abeta25-35- or LPS-induced neuronal inflammation via modulation of NF-kappaB signaling, Neuroscience, 355, 188, 10.1016/j.neuroscience.2017.05.005 · DOI
  25. Pryor, 2014, Huntingtin promotes mTORC1 signaling in the pathogenesis of Huntington's disease, Sci Signal, 7, ra103, 10.1126/scisignal.2005633 · DOI
  26. Masini, 2018, Inhibition of mTORC1 signaling reverts cognitive and affective deficits in a mouse model of Parkinson's disease, Front Neurol, 9, 208, 10.3389/fneur.2018.00208 · DOI
  27. Harayama, 2018, Understanding the diversity of membrane lipid composition, Nature reviews. Molecular cell biology, 19, 281, 10.1038/nrm.2017.138 · DOI
  28. Dimas, 2019, CNS myelination and remyelination depend on fatty acid synthesis by oligodendrocytes, Elife, 8, 10.7554/eLife.44702 · DOI · Paper page
  29. Lebrun-Julien, 2014, Balanced mTORC1 activity in oligodendrocytes is required for accurate CNS myelination, The Journal of neuroscience : the official journal of the Society for Neuroscience, 34, 8432, 10.1523/JNEUROSCI.1105-14.2014 · DOI
  30. Sachs, 2014, A new model of cuprizone-mediated demyelination/remyelination, ASN Neuro, 6, 10.1177/1759091414551955 · DOI
  31. Harrington, 2010, Oligodendrocyte PTEN is required for myelin and axonal integrity, not remyelination, Annals of neurology, 68, 703, 10.1002/ana.22090 · DOI
  32. Knobloch, 2013, Metabolic control of adult neural stem cell activity by Fasn-dependent lipogenesis, Nature, 493, 226, 10.1038/nature11689 · DOI
  33. Ziegler, 2017, Cell-autonomous control of neuronal dendrite expansion via the fatty acid synthesis regulator SREBP, Cell reports, 21, 3346, 10.1016/j.celrep.2017.11.069 · DOI
  34. Guillou, 2010, The key roles of elongases and desaturases in mammalian fatty acid metabolism: Insights from transgenic mice, Prog Lipid Res, 49, 186, 10.1016/j.plipres.2009.12.002 · DOI
  35. Jakobsson, 2006, Fatty acid elongases in mammals: their regulation and roles in metabolism, Prog Lipid Res, 45, 237, 10.1016/j.plipres.2006.01.004 · DOI · Paper page
  36. Li, 2018, Association of GALC, ZNF184, IL1R2 and ELOVL7 With Parkinson's Disease in Southern Chinese, Front Aging Neurosci, 10, 402, 10.3389/fnagi.2018.00402 · DOI
  37. Ozaki, 2015, A Novel mutation in ELOVL4 leading to spinocerebellar ataxia (SCA) with the hot cross bun sign but lacking erythrokeratodermia: a broadened spectrum of SCA34, JAMA Neurol, 72, 797, 10.1001/jamaneurol.2015.0610 · DOI · Paper page
  38. Mir, 2014, A novel recessive mutation in the gene ELOVL4 causes a neuro-ichthyotic disorder with variable expressivity, BMC Med Genet, 15, 10.1186/1471-2350-15-25 · DOI
  39. Hamilton, 2015, Aberrant lipid metabolism in the Forebrain Niche suppresses adult neural stem cell proliferation in an animal model of Alzheimer's disease, Cell stem cell, 17, 397, 10.1016/j.stem.2015.08.001 · DOI · Paper page
  40. Singh, 2011, HDAC inhibitor SAHA normalizes the levels of VLCFAs in human skin fibroblasts from X-ALD patients and downregulates the expression of proinflammatory cytokines in Abcd1/2-silenced mouse astrocytes, Journal of lipid research, 52, 2056, 10.1194/jlr.M017491 · DOI
  41. Senanayake, 2015, Metabolic dysfunctions in multiple sclerosis: implications as to causation, early detection, and treatment, a case control study, BMC neurology, 15, 10.1186/s12883-015-0411-4 · DOI
  42. Zhao, 2017, Elovl6 deficiency improves glycemic control in diabetic db/db mice by expanding beta-cell mass and increasing insulin secretory capacity, Diabetes, 66, 1833, 10.2337/db16-1277 · DOI
  43. Matsuzaka, 2012, Elovl6 promotes nonalcoholic steatohepatitis, Hepatology, 56, 2199, 10.1002/hep.25932 · DOI
  44. Nakamura, 2018, Elovl6 regulates mechanical damage-induced keratinocyte death and skin inflammation, Cell Death Dis, 9, 1181, 10.1038/s41419-018-1226-1 · DOI
  45. Talamonti, 2017, Impairment of systemic DHA synthesis affects macrophage plasticity and polarization: implications for DHA supplementation during inflammation, Cell Mol Life Sci, 74, 2815, 10.1007/s00018-017-2498-9 · DOI
  46. Chiurchiu, 2016, Proresolving lipid mediators resolvin D1, resolvin D2, and maresin 1 are critical in modulating T cell responses, Sci Transl Med, 8, 353ra111, 10.1126/scitranslmed.aaf7483 · DOI
  47. Robichaud, 2018, Polyunsaturated fatty acid elongation and desaturation in activated human T-cells: ELOVL5 is the key elongase, Journal of lipid research, 59, 2383, 10.1194/jlr.M090050 · DOI
  48. Sassa, 2014, Lorenzo's oil inhibits ELOVL1 and lowers the level of sphingomyelin with a saturated very long-chain fatty acid, Journal of lipid research, 55, 524, 10.1194/jlr.M044586 · DOI
  49. Shin, 2009, Dicer ablation in oligodendrocytes provokes neuronal impairment in mice, Annals of neurology, 66, 843, 10.1002/ana.21927 · DOI
  50. Hopiavuori, 2018, Homozygous expression of mutant ELOVL4 leads to seizures and death in a novel animal model of very long-chain fatty acid deficiency, Mol Neurobiol, 55, 1795, 10.1007/s12035-017-0824-8 · DOI
  51. Deak, 2019, Novel cellular functions of very long chain-fatty acids: insight from ELOVL4 mutations, Frontiers in cellular neuroscience, 13, 428, 10.3389/fncel.2019.00428 · DOI
  52. Sassa, 2013, Impaired epidermal permeability barrier in mice lacking elovl1, the gene responsible for very-long-chain fatty acid production, Molecular and cellular biology, 33, 2787, 10.1128/MCB.00192-13 · DOI
  53. Vasireddy, 2007, Loss of functional ELOVL4 depletes very long-chain fatty acids (> or =C28) and the unique omega-O-acylceramides in skin leading to neonatal death, Hum Mol Genet, 16, 471, 10.1093/hmg/ddl480 · DOI
  54. Lee, 2016, Fatty acid desaturases, polyunsaturated fatty acid regulation, and biotechnological advances, Nutrients, 8, 10.3390/nu8010023 · DOI
  55. Nakamura, 2004, Structure, function, and dietary regulation of delta6, delta5, and delta9 desaturases, Annu Rev Nutr, 24, 345, 10.1146/annurev.nutr.24.121803.063211 · DOI
  56. Paton, 2009, Biochemical and physiological function of stearoyl-CoA desaturase, Am J Physiol Endocrinol Metab, 297, E28, 10.1152/ajpendo.90897.2008 · DOI
  57. Yeoh, 2016, Deficiency of stearoyl-CoA desaturase-1 aggravates colitogenic potential of adoptively transferred effector T cells, Am J Physiol Gastrointest Liver Physiol, 311, G713, 10.1152/ajpgi.00174.2016 · DOI
  58. Brown, 2008, Inhibition of stearoyl-coenzyme A desaturase 1 dissociates insulin resistance and obesity from atherosclerosis, Circulation, 118, 1467, 10.1161/CIRCULATIONAHA.108.793182 · DOI
  59. Erbay, 2009, Reducing endoplasmic reticulum stress through a macrophage lipid chaperone alleviates atherosclerosis, Nature medicine, 15, 1383, 10.1038/nm.2067 · DOI
  60. Monk, 2014, Antagonizing arachidonic acid-derived eicosanoids reduces inflammatory Th17 and Th1 cell-mediated inflammation and colitis severity, Mediators of inflammation, 2014, 917149, 10.1155/2014/917149 · DOI
  61. Stoffel, 2008, Delta6-desaturase (FADS2) deficiency unveils the role of omega3- and omega6-polyunsaturated fatty acids, EMBO J, 27, 2281, 10.1038/emboj.2008.156 · DOI
  62. Uryu, 2003, beta-Amyloid-specific upregulation of stearoyl coenzyme A desaturase-1 in macrophages, Biochem Biophys Res Commun, 303, 302, 10.1016/S0006-291X(03)00334-6 · DOI
  63. Polo-Hernandez, 2014, Oleic acid synthesized by stearoyl-CoA desaturase (SCD-1) in the lateral periventricular zone of the developing rat brain mediates neuronal growth, migration and the arrangement of prospective synapses, Brain research, 1570, 13, 10.1016/j.brainres.2014.04.038 · DOI
  64. Tabernero, 2001, Neuronal differentiation is triggered by oleic acid synthesized and released by astrocytes, J Neurochem, 79, 606, 10.1046/j.1471-4159.2001.00598.x · DOI
  65. Sinner, 2012, StearoylCoA desaturase-5: a novel regulator of neuronal cell proliferation and differentiation, PloS one, 7, 10.1371/journal.pone.0039787 · DOI
  66. Vincent, 2018, Inhibiting stearoyl-CoA desaturase ameliorates alpha-synuclein cytotoxicity, Cell reports, 25, 2742, 10.1016/j.celrep.2018.11.028 · DOI
  67. Moore, 2001, Polyunsaturated fatty acid synthesis and release by brain-derived cells in vitro, J Mol Neurosci, 16, 195, 10.1385/JMN:16:2-3:195 · DOI
  68. Zhang, 2014, Opportunities and challenges in developing stearoyl-coenzyme A desaturase-1 inhibitors as novel therapeutics for human disease, Journal of medicinal chemistry, 57, 5039, 10.1021/jm401516c · DOI
  69. Liu, 2010, Recent advances in stearoyl-CoA desaturase 1 inhibitors for dyslipidemia and obesity, Curr Top Med Chem, 10, 419, 10.2174/156802610790980594 · DOI
  70. Igal, 2016, Stearoyl CoA desaturase-1: New insights into a central regulator of cancer metabolism, Biochimica et biophysica acta, 1861, 1865, 10.1016/j.bbalip.2016.09.009 · DOI
  71. Brown, 2010, Stearoyl-coenzyme A desaturase 1 inhibition and the metabolic syndrome: considerations for future drug discovery, Curr Opin Lipidol, 21, 192, 10.1097/MOL.0b013e32833854ac · DOI
  72. Ayala, 2014, Lipid peroxidation: production, metabolism, and signaling mechanisms of malondialdehyde and 4-hydroxy-2-nonenal, Oxid Med Cell Longev, 2014, 10.1155/2014/360438 · DOI
  73. Poli, 2004, Oxidative stress and cell signalling, Curr Med Chem, 11, 1163, 10.2174/0929867043365323 · DOI
  74. Pillon, 2012, The lipid peroxidation by-product 4-hydroxy-2-nonenal (4-HNE) induces insulin resistance in skeletal muscle through both carbonyl and oxidative stress, Endocrinology, 153, 2099, 10.1210/en.2011-1957 · DOI
  75. Kang, 2011, Hepatotoxicity and nephrotoxicity produced by 4-hydroxy-2-nonenal (4-HNE) following 4-week oral administration to Sprague-Dawley rats, J Toxicol Environ Health A, 74, 779, 10.1080/15287394.2011.567952 · DOI
  76. Karihtala, 2011, Divergent behaviour of oxidative stress markers 8-hydroxydeoxyguanosine (8-OHdG) and 4-hydroxy-2-nonenal (HNE) in breast carcinogenesis, Histopathology, 58, 854, 10.1111/j.1365-2559.2011.03835.x · DOI
  77. Mattson, 2009, Roles of the lipid peroxidation product 4-hydroxynonenal in obesity, the metabolic syndrome, and associated vascular and neurodegenerative disorders, Exp Gerontol, 44, 625, 10.1016/j.exger.2009.07.003 · DOI
  78. Butterfield, 2010, Involvements of the lipid peroxidation product, HNE, in the pathogenesis and progression of Alzheimer's disease, Biochim Biophys Acta, 1801, 924, 10.1016/j.bbalip.2010.02.005 · DOI
  79. McKracken, 2001, 4-Hydroxynonenal immunoreactivity is increased in human hippocampus after global ischemia, Brain Pathol, 11, 414, 10.1111/j.1750-3639.2001.tb00409.x · DOI
  80. Kumagai, 2004, A lipid peroxidation-derived inflammatory mediator: identification of 4-hydroxy-2-nonenal as a potential inducer of cyclooxygenase-2 in macrophages, J Biol Chem, 279, 48389, 10.1074/jbc.M409935200 · DOI
  81. Yadav, 2013, Regulation of NF-kappaB-induced inflammatory signaling by lipid peroxidation-derived aldehydes, Oxid Med Cell Longev, 2013, 10.1155/2013/690545 · DOI
  82. Yang, 2018, Unveiling anti-oxidative and anti-inflammatory effects of docosahexaenoic acid and its lipid peroxidation product on lipopolysaccharide-stimulated BV-2 microglial cells, Journal of neuroinflammation, 15, 10.1186/s12974-018-1232-3 · DOI
  83. Schild, 2002, The activity of PPAR gamma in primary human trophoblasts is enhanced by oxidized lipids, J Clin Endocrinol Metab, 87, 1105
  84. Nagy, 1998, Oxidized LDL regulates macrophage gene expression through ligand activation of PPARgamma, Cell, 93, 229, 10.1016/S0092-8674(00)81574-3 · DOI
  85. Ljubisavljevic, 2013, Suppression of the lipid peroxidation process in the CNS reduces neurological expression of experimentally induced autoimmune encephalomyelitis, Folia Neuropathol, 51, 51, 10.5114/fn.2013.34196 · DOI
  86. Sosa, 2015, IFN-gamma ameliorates autoimmune encephalomyelitis by limiting myelin lipid peroxidation, Proceedings of the National Academy of Sciences of the United States of America, 112, E5038
  87. Wang, 2014, Oxidative stress induced by lipid peroxidation is related with inflammation of demyelination and neurodegeneration in multiple sclerosis, Eur Neurol, 72, 249, 10.1159/000363515 · DOI
  88. Braughler, 1992, Involvement of lipid peroxidation in CNS injury, J Neurotrauma, 9, S1
  89. Bush, 2008, Therapeutics for Alzheimer's disease based on the metal hypothesis, Neurotherapeutics, 5, 421, 10.1016/j.nurt.2008.05.001 · DOI
  90. Dexter, 1989, Basal lipid peroxidation in substantia nigra is increased in Parkinson's disease, J Neurochem, 52, 381, 10.1111/j.1471-4159.1989.tb09133.x · DOI
  91. Angelova, 2015, Lipid peroxidation is essential for alpha-synuclein-induced cell death, J Neurochem, 133, 582, 10.1111/jnc.13024 · DOI
  92. Do, 2019, Elovanoids counteract oligomeric beta-amyloid-induced gene expression and protect photoreceptors, Proceedings of the National Academy of Sciences of the United States of America, 116, 24317, 10.1073/pnas.1912959116 · DOI
  93. Bhattacharjee, 2017, Elovanoids are a novel class of homeostatic lipid mediators that protect neural cell integrity upon injury, Sci Adv, 3, 10.1126/sciadv.1700735 · DOI · Paper page
  94. Erny, 2015, Host microbiota constantly control maturation and function of microglia in the CNS, Nature neuroscience, 18, 965, 10.1038/nn.4030 · DOI · Paper page
  95. Haghikia, 2016, Dietary fatty acids directly impact central nervous system autoimmunity via the small intestine, Immunity, 44, 951, 10.1016/j.immuni.2016.04.006 · DOI · Paper page
  96. Ho, 2018, Protective roles of intestinal microbiota derived short chain fatty acids in Alzheimer's disease-type beta-amyloid neuropathological mechanisms, Expert review of neurotherapeutics, 18, 83, 10.1080/14737175.2018.1400909 · DOI · Paper page
  97. Laurent, 2013, Sodium butyrate improves locomotor impairment and early mortality in a rotenone-induced Drosophila model of Parkinson's disease, Neuroscience, 246, 382, 10.1016/j.neuroscience.2013.04.037 · DOI · Paper page
  98. Sharma, 2015, Beneficial effects of sodium butyrate in 6-OHDA induced neurotoxicity and behavioral abnormalities: modulation of histone deacetylase activity, Behav Brain Res, 291, 306, 10.1016/j.bbr.2015.05.052 · DOI · Paper page
  99. Langley, 2008, Pulse inhibition of histone deacetylases induces complete resistance to oxidative death in cortical neurons without toxicity and reveals a role for cytoplasmic p21(waf1/cip1) in cell cycle-independent neuroprotection, The Journal of neuroscience : the official journal of the Society for Neuroscience, 28, 163, 10.1523/JNEUROSCI.3200-07.2008 · DOI
  100. Kim, 2014, HDAC inhibitors mitigate ischemia-induced oligodendrocyte damage: potential roles of oligodendrogenesis, VEGF, and anti-inflammation, Am J Transl Res, 6, 206
  101. Braniste, 2014, The gut microbiota influences blood-brain barrier permeability in mice, Sci Transl Med, 6, 10.1126/scitranslmed.3009759 · DOI · Paper page
  102. Sherry, 2010, Sickness behavior induced by endotoxin can be mitigated by the dietary soluble fiber, pectin, through up-regulation of IL-4 and Th2 polarization, Brain, behavior, and immunity, 24, 631, 10.1016/j.bbi.2010.01.015 · DOI
  103. Govindarajan, 2011, Sodium butyrate improves memory function in an Alzheimer's disease mouse model when administered at an advanced stage of disease progression, J Alzheimers Dis, 26, 187, 10.3233/JAD-2011-110080 · DOI · Paper page
  104. Dash, 2009, Histone deactylase inhibition combined with behavioral therapy enhances learning and memory following traumatic brain injury, Neuroscience, 163, 1, 10.1016/j.neuroscience.2009.06.028 · DOI
  105. Unger, 2016, Short chain fatty acids and gut microbiota differ between patients with Parkinson's disease and age-matched controls, Parkinsonism Relat Disord, 32, 66, 10.1016/j.parkreldis.2016.08.019 · DOI · Paper page
  106. Trauner, 1985, Effect of octanoate injection on rat blood-brain barrier, Pediatr Neurol, 1, 20, 10.1016/0887-8994(85)90004-9 · DOI
  107. Wang, 2006, Medium-chain fatty acids as ligands for orphan G protein-coupled receptor GPR84, The Journal of biological chemistry, 281, 34457, 10.1074/jbc.M608019200 · DOI
  108. Alvarez-Curto, 2016, Metabolism meets immunity: The role of free fatty acid receptors in the immune system, Biochemical pharmacology, 114, 3, 10.1016/j.bcp.2016.03.017 · DOI
  109. Bouchard, 2007, G protein-coupled receptor 84, a microglia-associated protein expressed in neuroinflammatory conditions, Glia, 55, 790, 10.1002/glia.20506 · DOI
  110. Nicol, 2015, The role of G-protein receptor 84 in experimental neuropathic pain, The Journal of neuroscience : the official journal of the Society for Neuroscience, 35, 8959, 10.1523/JNEUROSCI.3558-14.2015 · DOI
  111. Venkataraman, 2005, The G-protein coupled receptor, GPR84 regulates IL-4 production by T lymphocytes in response to CD3 crosslinking, Immunology letters, 101, 144, 10.1016/j.imlet.2005.05.010 · DOI
  112. Recio, 2018, Activation of the immune-metabolic receptor GPR84 Enhances inflammation and phagocytosis in macrophages, Frontiers in immunology, 9, 1419, 10.3389/fimmu.2018.01419 · DOI
  113. Gamo, 2008, G-protein-coupled receptor screen reveals a role for chemokine receptor CCR5 in suppressing microglial neurotoxicity, The Journal of neuroscience : the official journal of the Society for Neuroscience, 28, 11980, 10.1523/JNEUROSCI.2920-08.2008 · DOI
  114. Bedard, 2007, Identification of genes preferentially expressed by microglia and upregulated during cuprizone-induced inflammation, Glia, 55, 777, 10.1002/glia.20477 · DOI
  115. Audoy-Remus, 2015, GPR84 deficiency reduces microgliosis, but accelerates dendritic degeneration and cognitive decline in a mouse model of Alzheimer's disease, Brain, behavior, and immunity, 46, 112, 10.1016/j.bbi.2015.01.010 · DOI
  116. Chang, 2013, Seizure control by ketogenic diet-associated medium chain fatty acids, Neuropharmacology, 69, 105, 10.1016/j.neuropharm.2012.11.004 · DOI
  117. Chang, 2016, Seizure control by decanoic acid through direct AMPA receptor inhibition, Brain : a journal of neurology, 139, 431, 10.1093/brain/awv325 · DOI
  118. Neal, 2009, A randomized trial of classical and medium-chain triglyceride ketogenic diets in the treatment of childhood epilepsy, Epilepsia, 50, 1109, 10.1111/j.1528-1167.2008.01870.x · DOI
  119. Taylor, 2018, Feasibility and efficacy data from a ketogenic diet intervention in Alzheimer's disease, Alzheimers Dement (N Y), 4, 28, 10.1016/j.trci.2017.11.002 · DOI
  120. Mochel, 2010, Dietary anaplerotic therapy improves peripheral tissue energy metabolism in patients with Huntington's disease, Eur J Hum Genet, 18, 1057, 10.1038/ejhg.2010.72 · DOI
  121. Angela, 2016, Fatty acid metabolic reprogramming via mTOR-mediated inductions of PPARgamma directs early activation of T cells, Nat Commun, 7, 13683, 10.1038/ncomms13683 · DOI
  122. Gupta, 2012, Saturated long-chain fatty acids activate inflammatory signaling in astrocytes, J Neurochem, 120, 1060, 10.1111/j.1471-4159.2012.07660.x · DOI
  123. Milanski, 2009, Saturated fatty acids produce an inflammatory response predominantly through the activation of TLR4 signaling in hypothalamus: implications for the pathogenesis of obesity, The Journal of neuroscience : the official journal of the Society for Neuroscience, 29, 359, 10.1523/JNEUROSCI.2760-08.2009 · DOI · Paper page
  124. Dutheil, 2016, High-fat diet induced anxiety and anhedonia: impact on brain homeostasis and inflammation, Neuropsychopharmacology, 41, 1874, 10.1038/npp.2015.357 · DOI · Paper page
  125. Park, 2011, Lipotoxicity of palmitic acid on neural progenitor cells and hippocampal neurogenesis, Toxicol Res, 27, 103, 10.5487/TR.2011.27.2.103 · DOI
  126. Mayer, 2010, Palmitate attenuates insulin signaling and induces endoplasmic reticulum stress and apoptosis in hypothalamic neurons: rescue of resistance and apoptosis through adenosine 5' monophosphate-activated protein kinase activation, Endocrinology, 151, 576, 10.1210/en.2009-1122 · DOI
  127. Patil, 2005, Palmitic and stearic fatty acids induce Alzheimer-like hyperphosphorylation of tau in primary rat cortical neurons, Neuroscience letters, 384, 288, 10.1016/j.neulet.2005.05.003 · DOI
  128. Schommer, 2018, Palmitic acid-enriched diet increases alpha-synuclein and tyrosine hydroxylase expression levels in the mouse brain, Front Neurosci, 12, 552, 10.3389/fnins.2018.00552 · DOI
  129. Kim, 2017, Palmitic acid-BSA enhances amyloid-beta production through GPR40-mediated dual pathways in neuronal cells: Involvement of the Akt/mTOR/HIF-1alpha and Akt/NF-kappaB pathways, Sci Rep, 7, 4335, 10.1038/s41598-017-04175-w · DOI
  130. Yoon, 2016, Interplay between exercise and dietary fat modulates myelinogenesis in the central nervous system, Biochimica et biophysica acta, 1862, 545, 10.1016/j.bbadis.2016.01.019 · DOI
  131. Hon, 2009, Membrane saturated fatty acids and disease progression in multiple sclerosis patients, Metab Brain Dis, 24, 561, 10.1007/s11011-009-9159-0 · DOI
  132. Nasaruddin, 2016, Wide-ranging alterations in the brain fatty acid complement of subjects with late Alzheimer's disease as detected by GC-MS, Am J Transl Res, 8, 154
  133. Passos, 2016, Differential effects of palmitoleic acid on human lymphocyte proliferation and function, Lipids Health Dis, 15, 217, 10.1186/s12944-016-0385-2 · DOI
  134. Oh, 2009, Oleic acid reduces lipopolysaccharide-induced expression of iNOS and COX-2 in BV2 murine microglial cells: possible involvement of reactive oxygen species, p38 MAPK, and IKK/NF-kappaB signaling pathways, Neuroscience letters, 464, 93, 10.1016/j.neulet.2009.08.040 · DOI
  135. Souza, 2017, Palmitoleic acid reduces the inflammation in LPS-stimulated macrophages by inhibition of NFkappaB, independently of PPARs, Clin Exp Pharmacol Physiol, 44, 566, 10.1111/1440-1681.12736 · DOI
  136. Pereira, 2014, Anti-inflammatory effect of unsaturated fatty acids and Ergosta-7,22-dien-3-ol from Marthasterias glacialis: prevention of CHOP-mediated ER-stress and NF-kappaB activation, PloS one, 9, 10.1371/journal.pone.0088341 · DOI
  137. Cappa, 2012, A mixture of oleic, erucic and conjugated linoleic acids modulates cerebrospinal fluid inflammatory markers and improve somatosensorial evoked potential in X-linked adrenoleukodystrophy female carriers, J Inherit Metab Dis, 35, 899, 10.1007/s10545-011-9432-3 · DOI · Paper page
  138. Song, 2019, Neuroprotective effects of oleic acid in rodent models of cerebral ischaemia, Sci Rep, 9, 10732, 10.1038/s41598-019-47057-z · DOI
  139. Johnson, 1997, Structural requirements and cell-type specificity for ligand activation of peroxisome proliferator-activated receptors, J Steroid Biochem Mol Biol, 63, 1, 10.1016/S0960-0760(97)00064-2 · DOI
  140. Altinoz, 2019, PPAR-delta and erucic acid in multiple sclerosis and Alzheimer's Disease. Likely benefits in terms of immunity and metabolism, Int Immunopharmacol, 69, 245, 10.1016/j.intimp.2019.01.057 · DOI
  141. Polo-Hernandez, 2010, Oleic acid synthesized in the periventricular zone promotes axonogenesis in the striatum during brain development, J Neurochem, 114, 1756, 10.1111/j.1471-4159.2010.06891.x · DOI
  142. Ghareghani, 2017, Safflower seed oil, containing oleic acid and palmitic acid, enhances the stemness of cultured embryonic neural stem cells through notch1 and induces neuronal differentiation, Front Neurosci, 11, 446, 10.3389/fnins.2017.00446 · DOI
  143. Amtul, 2011, Oleic acid ameliorates amyloidosis in cellular and mouse models of Alzheimer's disease, Brain pathology, 21, 321, 10.1111/j.1750-3639.2010.00449.x · DOI
  144. Kim, 2005, Unsaturated fatty acids induce cytotoxic aggregate formation of amyotrophic lateral sclerosis-linked superoxide dismutase 1 mutants, The Journal of biological chemistry, 280, 21515, 10.1074/jbc.M502230200 · DOI
  145. Liu, 2004, Fatty acids increase presenilin-1 levels and [gamma]-secretase activity in PSwt-1 cells, Journal of lipid research, 45, 2368, 10.1194/jlr.M400317-JLR200 · DOI
  146. Wilson, 1997, Free fatty acids stimulate the polymerization of tau and amyloid beta peptides. In vitro evidence for a common effector of pathogenesis in Alzheimer's disease, The American journal of pathology, 150, 2181
  147. Guan, 1999, Decrease and structural modifications of phosphatidylethanolamine plasmalogen in the brain with Alzheimer disease, Journal of neuropathology and experimental neurology, 58, 740, 10.1097/00005072-199907000-00008 · DOI
  148. Trepanier, 2018, Phosphatidylcholine 36:1 concentration decreases along with demyelination in the cuprizone animal model and in post-mortem multiple sclerosis brain tissue, J Neurochem, 145, 504, 10.1111/jnc.14335 · DOI
  149. Fonteh, 2014, Human cerebrospinal fluid fatty acid levels differ between supernatant fluid and brain-derived nanoparticle fractions, and are altered in Alzheimer's disease, PloS one, 9, 10.1371/journal.pone.0100519 · DOI
  150. Nogueras, 2019, Lipid profile of cerebrospinal fluid in multiple sclerosis patients: a potential tool for diagnosis, Sci Rep, 9, 11313, 10.1038/s41598-019-47906-x · DOI
  151. Ouellet, 2009, Diffusion of docosahexaenoic and eicosapentaenoic acids through the blood-brain barrier: An in situ cerebral perfusion study, Neurochemistry international, 55, 476, 10.1016/j.neuint.2009.04.018 · DOI
  152. Orr, 2013, n-3 Polyunsaturated fatty acids in animal models with neuroinflammation, Prostaglandins Leukot Essent Fatty Acids, 88, 97, 10.1016/j.plefa.2012.05.008 · DOI
  153. Laye, 2018, Anti-inflammatory effects of omega-3 fatty acids in the brain: physiological mechanisms and relevance to pharmacology, Pharmacol Rev, 70, 12, 10.1124/pr.117.014092 · DOI · Paper page
  154. Allen, 2014, n-3 PUFAs reduce T-helper 17 cell differentiation by decreasing responsiveness to interleukin-6 in isolated mouse splenic CD4(+) T cells, J Nutr, 144, 1306, 10.3945/jn.114.194407 · DOI
  155. Ferrante, 1994, Neutrophil migration inhibitory properties of polyunsaturated fatty acids. The role of fatty acid structure, metabolism, and possible second messenger systems, The Journal of clinical investigation, 93, 1063, 10.1172/JCI117056 · DOI
  156. Vedin, 2008, Effects of docosahexaenoic acid-rich n-3 fatty acid supplementation on cytokine release from blood mononuclear leukocytes: the OmegAD study, Am J Clin Nutr, 87, 1616, 10.1093/ajcn/87.6.1616 · DOI · Paper page
  157. Tamtaji, 2019, The effects of omega-3 fatty acids and vitamin E co-supplementation on gene expression related to inflammation, insulin and lipid in patients with Parkinson's disease: a randomized, double-blind, placebo-controlled trial, Clin Neurol Neurosurg, 176, 116, 10.1016/j.clineuro.2018.12.006 · DOI
  158. Ramirez-Ramirez, 2013, Efficacy of fish oil on serum of TNF alpha , IL-1 beta , and IL-6 oxidative stress markers in multiple sclerosis treated with interferon beta-1b, Oxid Med Cell Longev, 2013, 709493, 10.1155/2013/709493 · DOI
  159. Schmitz, 2008, The opposing effects of n-3 and n-6 fatty acids, Prog Lipid Res, 47, 147, 10.1016/j.plipres.2007.12.004 · DOI · Paper page
  160. Kohli, 2009, Resolvins and protectins: mediating solutions to inflammation, British journal of pharmacology, 158, 960, 10.1111/j.1476-5381.2009.00290.x · DOI
  161. Basil, 2016, Specialized pro-resolving mediators: endogenous regulators of infection and inflammation, Nature reviews. Immunology, 16, 51, 10.1038/nri.2015.4 · DOI
  162. Innes, 2018, Omega-6 fatty acids and inflammation, Prostaglandins Leukot Essent Fatty Acids, 132, 41, 10.1016/j.plefa.2018.03.004 · DOI
  163. Chen, 2009, Effects of leukotriene B4 and prostaglandin E2 on the differentiation of murine Foxp3+ T regulatory cells and Th17 cells, Prostaglandins Leukot Essent Fatty Acids, 80, 195, 10.1016/j.plefa.2009.01.006 · DOI
  164. Kumar, 2014, Exogenous addition of arachidonic acid to the culture media enhances the functionality of dendritic cells for their possible use in cancer immunotherapy, PloS one, 9, 10.1371/journal.pone.0111759 · DOI
  165. Hopperton, 2016, Brain omega-3 polyunsaturated fatty acids modulate microglia cell number and morphology in response to intracerebroventricular amyloid-beta 1-40 in mice, Journal of neuroinflammation, 13, 257, 10.1186/s12974-016-0721-5 · DOI
  166. Harbige, 2000, The protective effects of omega-6 fatty acids in experimental autoimmune encephalomyelitis (EAE) in relation to transforming growth factor-beta 1 (TGF-beta1) up-regulation and increased prostaglandin E2 (PGE2) production, Clin Exp Immunol, 122, 445, 10.1046/j.1365-2249.2000.01399.x · DOI
  167. Marangoni, 2020, Dietary linoleic acid and human health: focus on cardiovascular and cardiometabolic effects, Atherosclerosis, 292, 90, 10.1016/j.atherosclerosis.2019.11.018 · DOI
  168. Marklund, 2019, Biomarkers of dietary omega-6 fatty acids and incident cardiovascular disease and mortality, Circulation, 139, 2422, 10.1161/CIRCULATIONAHA.118.038908 · DOI
  169. Farinotti, 2012, Dietary interventions for multiple sclerosis, Cochrane Database Syst Rev, 12
  170. Silva, 2018, Wound healing and omega-6 fatty acids: from inflammation to repair, Mediators of inflammation, 2018, 2503950, 10.1155/2018/2503950 · DOI
  171. Hussein, 2005, Long-chain conversion of [13C]linoleic acid and alpha-linolenic acid in response to marked changes in their dietary intake in men, Journal of Lipid Research, 46, 269, 10.1194/jlr.M400225-JLR200 · DOI
  172. Hejr, 2017, The ratio of 1/3 linoleic acid to alpha linolenic acid is optimal for oligodendrogenesis of embryonic neural stem cells, Neuroscience letters, 651, 216, 10.1016/j.neulet.2017.05.020 · DOI
  173. Katakura, 2013, Omega-3 polyunsaturated Fatty acids enhance neuronal differentiation in cultured rat neural stem cells, Stem Cells Int, 2013, 490476, 10.1155/2013/490476 · DOI
  174. Calderon, 2004, Docosahexaenoic acid promotes neurite growth in hippocampal neurons, J Neurochem, 90, 979, 10.1111/j.1471-4159.2004.02520.x · DOI
  175. Robson, 2010, Omega-3 polyunsaturated fatty acids increase the neurite outgrowth of rat sensory neurones throughout development and in aged animals, Neurobiology of aging, 31, 678, 10.1016/j.neurobiolaging.2008.05.027 · DOI
  176. Bernardo, 2017, Docosahexaenoic acid promotes oligodendrocyte differentiation via PPAR-gamma signalling and prevents tumor necrosis factor-alpha-dependent maturational arrest, Biochim Biophys Acta Mol Cell Biol Lipids, 1862, 1013, 10.1016/j.bbalip.2017.06.014 · DOI
  177. Lewkowicz, 2019, Naturally occurring nervonic acid ester improves myelin synthesis by human oligodendrocytes, Cells, 8, 10.3390/cells8080786 · DOI
  178. Siegert, 2017, The effect of omega-3 fatty acids on central nervous system remyelination in fat-1 mice, BMC Neurosci, 18, 19, 10.1186/s12868-016-0312-5 · DOI
  179. Torkildsen, 2009, Effects of dietary intervention on MRI activity, de- and remyelination in the cuprizone model for demyelination, Experimental neurology, 215, 160, 10.1016/j.expneurol.2008.09.026 · DOI
  180. Ward, 2010, Docosahexaenoic acid prevents white matter damage after spinal cord injury, J Neurotrauma, 27, 1769, 10.1089/neu.2010.1348 · DOI
  181. Huang, 2007, A combination of intravenous and dietary docosahexaenoic acid significantly improves outcome after spinal cord injury, Brain : a journal of neurology, 130, 3004, 10.1093/brain/awm223 · DOI
  182. Luo, 2014, Enriched endogenous omega-3 fatty acids in mice protect against global ischemia injury, Journal of lipid research, 55, 1288, 10.1194/jlr.M046466 · DOI
  183. Chang, 2013, Docosahexaenoic acid reduces cellular inflammatory response following permanent focal cerebral ischemia in rats, J Nutr Biochem, 24, 2127, 10.1016/j.jnutbio.2013.08.004 · DOI
  184. Kwon, 2005, Arachidonic acid induces neuronal death through lipoxygenase and cytochrome P450 rather than cyclooxygenase, Journal of neuroscience research, 81, 73, 10.1002/jnr.20520 · DOI
  185. Kriem, 2005, Cytosolic phospholipase A2 mediates neuronal apoptosis induced by soluble oligomers of the amyloid-beta peptide, FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 19, 85, 10.1096/fj.04-1807fje · DOI
  186. Fraser, 1993, Arachidonic acid inhibits sodium currents and synaptic transmission in cultured striatal neurons, Neuron, 11, 633, 10.1016/0896-6273(93)90075-3 · DOI
  187. Amtul, 2012, Detrimental effects of arachidonic acid and its metabolites in cellular and mouse models of Alzheimer's disease: structural insight, Neurobiology of aging, 33, 10.1016/j.neurobiolaging.2011.07.014 · DOI
  188. Thomas, 2017, Dietary arachidonic acid increases deleterious effects of amyloid-beta oligomers on learning abilities and expression of AMPA receptors: putative role of the ACSL4-cPLA2 balance, Alzheimers Res Ther, 9, 69, 10.1186/s13195-017-0295-1 · DOI
  189. Hatanaka, 2016, Essentiality of arachidonic acid intake in murine early development, Prostaglandins Leukot Essent Fatty Acids, 108, 51, 10.1016/j.plefa.2016.03.007 · DOI
  190. Harauma, 2017, The essentiality of arachidonic acid in addition to docosahexaenoic acid for brain growth and function, Prostaglandins Leukot Essent Fatty Acids, 116, 9, 10.1016/j.plefa.2016.11.002 · DOI
  191. Zhao, 2011, Maternal arachidonic acid supplementation improves neurodevelopment in young adult offspring from rat dams with and without diabetes, Prostaglandins Leukot Essent Fatty Acids, 84, 63, 10.1016/j.plefa.2010.08.009 · DOI
  192. Theda, 1992, Phospholipids in X-linked adrenoleukodystrophy white matter: fatty acid abnormalities before the onset of demyelination, Journal of the neurological sciences, 110, 195, 10.1016/0022-510X(92)90028-J · DOI · Paper page
  193. Sharp, 1991, Molecular species of phosphatidylcholine containing very long chain fatty acids in human brain: enrichment in X-linked adrenoleukodystrophy brain and diseases of peroxisome biogenesis brain, J Neurochem, 56, 30, 10.1111/j.1471-4159.1991.tb02558.x · DOI
  194. Marchetti, 2018, Inflammatory profile in X-linked adrenoleukodystrophy patients: understanding disease progression, J Cell Biochem, 119, 1223, 10.1002/jcb.26295 · DOI
  195. Paintlia, 2003, Correlation of very long chain fatty acid accumulation and inflammatory disease progression in childhood X-ALD: implications for potential therapies, Neurobiology of disease, 14, 425, 10.1016/j.nbd.2003.08.013 · DOI
  196. Weber, 2014, X-linked adrenoleukodystrophy: very long-chain fatty acid metabolism is severely impaired in monocytes but not in lymphocytes, Hum Mol Genet, 23, 2542, 10.1093/hmg/ddt645 · DOI · Paper page
  197. Yanagisawa, 2008, Enhanced production of nitric oxide, reactive oxygen species, and pro-inflammatory cytokines in very long chain saturated fatty acid-accumulated macrophages, Lipids Health Dis, 7, 48, 10.1186/1476-511X-7-48 · DOI · Paper page
  198. Schaumburg, 1975, Adrenoleukodystrophy. A clinical and pathological study of 17 cases, Archives of neurology, 32, 577, 10.1001/archneur.1975.00490510033001 · DOI · Paper page
  199. Eichler, 2008, Is microglial apoptosis an early pathogenic change in cerebral X-linked adrenoleukodystrophy?, Annals of neurology, 63, 729, 10.1002/ana.21391 · DOI · Paper page
  200. Karasawa, 2018, Saturated fatty acids undergo intracellular crystallization and activate the NLRP3 inflammasome in macrophages, Arterioscler Thromb Vasc Biol, 38, 744, 10.1161/ATVBAHA.117.310581 · DOI · Paper page

200 of 253 shown

Cited by

Sorted by citations

See all 167

Metadata

Authors
Bogie, J. F. J., Haidar, M., Kooij, G., & Hendriks, J. J. A.
Venue
Advanced Drug Delivery Reviews
Publisher
Elsevier BV
Published
2020
Volume
159
Pages
198-213
ISSN
0169-409X
Cited by
167
References
40
Language
en
Funders
  • Stichting MS Research (18-1023)
  • Interreg (EMR23)
  • Fonds Wetenschappelijk Onderzoek (G099618N, 12JG119N, 12J9116N)
  • Fondation Charcot (R-6832, R-8676)

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review