Conjugated Linoleic Acid and Brain Metabolism: A Possible Anti-Neuroinflammatory Role Mediated by PPARα Activation

Fatty acids play a crucial role in the brain as specific receptor ligands and as precursors of bioactive metabolites. Conjugated linoleic acid (CLA), a group of positional and geometric isomers of linoleic acid (LA, 18:2 n-6) present in meat and dairy products of ruminants and synthesized endogenous...

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Main Authors: Elisabetta Murru, Gianfranca Carta, Claudia Manca, Valeria Sogos, Marco Pistis, Miriam Melis, Sebastiano Banni
Format: Article
Language:English
Published: Frontiers Media S.A. 2021-01-01
Series:Frontiers in Pharmacology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fphar.2020.587140/full
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author Elisabetta Murru
Gianfranca Carta
Claudia Manca
Valeria Sogos
Marco Pistis
Marco Pistis
Miriam Melis
Sebastiano Banni
author_facet Elisabetta Murru
Gianfranca Carta
Claudia Manca
Valeria Sogos
Marco Pistis
Marco Pistis
Miriam Melis
Sebastiano Banni
author_sort Elisabetta Murru
collection DOAJ
description Fatty acids play a crucial role in the brain as specific receptor ligands and as precursors of bioactive metabolites. Conjugated linoleic acid (CLA), a group of positional and geometric isomers of linoleic acid (LA, 18:2 n-6) present in meat and dairy products of ruminants and synthesized endogenously in non-ruminants and humans, has been shown to possess different nutritional properties associated with health benefits. Its ability to bind to peroxisome proliferator-activated receptor (PPAR) α, a nuclear receptor key regulator of fatty acid metabolism and inflammatory responses, partly mediates these beneficial effects. CLA is incorporated and metabolized into brain tissue where induces the biosynthesis of endogenous PPARα ligands palmitoylethanolamide (PEA) and oleoylethanolamide (OEA), likely through a positive feedback mechanism where PPARα activation sustains its own cellular effects through ligand biosynthesis. In addition to PPARα, PEA and OEA may as well bind to other receptors such as TRPV1, further extending CLA own anti-neuroinflammatory actions. Future studies are needed to investigate whether dietary CLA may exert anti-inflammatory activity, particularly in the setting of neurodegenerative diseases and neuropsychiatric disorders with a neuroinflammatory basis.
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spelling doaj.art-32f3987736d24c67bd811471d9a50b332022-12-21T23:16:44ZengFrontiers Media S.A.Frontiers in Pharmacology1663-98122021-01-011110.3389/fphar.2020.587140587140Conjugated Linoleic Acid and Brain Metabolism: A Possible Anti-Neuroinflammatory Role Mediated by PPARα ActivationElisabetta Murru0Gianfranca Carta1Claudia Manca2Valeria Sogos3Marco Pistis4Marco Pistis5Miriam Melis6Sebastiano Banni7Department of Biomedical Sciences, University of Cagliari, Monserrato, ItalyDepartment of Biomedical Sciences, University of Cagliari, Monserrato, ItalyDepartment of Biomedical Sciences, University of Cagliari, Monserrato, ItalyDepartment of Biomedical Sciences, University of Cagliari, Monserrato, ItalyDepartment of Biomedical Sciences, University of Cagliari, Monserrato, ItalyNeuroscience Institute, National Research Council of Italy (CNR), Cagliari, ItalyDepartment of Biomedical Sciences, University of Cagliari, Monserrato, ItalyDepartment of Biomedical Sciences, University of Cagliari, Monserrato, ItalyFatty acids play a crucial role in the brain as specific receptor ligands and as precursors of bioactive metabolites. Conjugated linoleic acid (CLA), a group of positional and geometric isomers of linoleic acid (LA, 18:2 n-6) present in meat and dairy products of ruminants and synthesized endogenously in non-ruminants and humans, has been shown to possess different nutritional properties associated with health benefits. Its ability to bind to peroxisome proliferator-activated receptor (PPAR) α, a nuclear receptor key regulator of fatty acid metabolism and inflammatory responses, partly mediates these beneficial effects. CLA is incorporated and metabolized into brain tissue where induces the biosynthesis of endogenous PPARα ligands palmitoylethanolamide (PEA) and oleoylethanolamide (OEA), likely through a positive feedback mechanism where PPARα activation sustains its own cellular effects through ligand biosynthesis. In addition to PPARα, PEA and OEA may as well bind to other receptors such as TRPV1, further extending CLA own anti-neuroinflammatory actions. Future studies are needed to investigate whether dietary CLA may exert anti-inflammatory activity, particularly in the setting of neurodegenerative diseases and neuropsychiatric disorders with a neuroinflammatory basis.https://www.frontiersin.org/articles/10.3389/fphar.2020.587140/fullconjugated linoleic acidperoxisome proliferator-activated receptor αbrainneuroinflammationlipid nutrition
spellingShingle Elisabetta Murru
Gianfranca Carta
Claudia Manca
Valeria Sogos
Marco Pistis
Marco Pistis
Miriam Melis
Sebastiano Banni
Conjugated Linoleic Acid and Brain Metabolism: A Possible Anti-Neuroinflammatory Role Mediated by PPARα Activation
Frontiers in Pharmacology
conjugated linoleic acid
peroxisome proliferator-activated receptor α
brain
neuroinflammation
lipid nutrition
title Conjugated Linoleic Acid and Brain Metabolism: A Possible Anti-Neuroinflammatory Role Mediated by PPARα Activation
title_full Conjugated Linoleic Acid and Brain Metabolism: A Possible Anti-Neuroinflammatory Role Mediated by PPARα Activation
title_fullStr Conjugated Linoleic Acid and Brain Metabolism: A Possible Anti-Neuroinflammatory Role Mediated by PPARα Activation
title_full_unstemmed Conjugated Linoleic Acid and Brain Metabolism: A Possible Anti-Neuroinflammatory Role Mediated by PPARα Activation
title_short Conjugated Linoleic Acid and Brain Metabolism: A Possible Anti-Neuroinflammatory Role Mediated by PPARα Activation
title_sort conjugated linoleic acid and brain metabolism a possible anti neuroinflammatory role mediated by pparα activation
topic conjugated linoleic acid
peroxisome proliferator-activated receptor α
brain
neuroinflammation
lipid nutrition
url https://www.frontiersin.org/articles/10.3389/fphar.2020.587140/full
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