Volume 23, Number 1, January-February 2016
|Number of page(s)||10|
|Section||Dossier: Lipids and Brain / Lipides et cerveau|
|Published online||19 January 2016|
N-3 PUFAs and neuroinflammatory processes in cognitive disorders
Acides gras polyinsaturés de la famille des oméga 3, processus neuroinflammatoires et troubles cognitifs
INRA, Nutrition et Neurobiologie Intégrée, UMR 1286,
2 Bordeaux University, Nutrition et Neurobiologie Intégrée, UMR 1286, Bordeaux, France
3 Laboratoire NutriNeuro, UMR INRA Université de Bordeaux 1286, UFR Pharmacie, CC34, 146, rue Léo Saignat, 33076 Bordeaux Cedex, France
* Correspondence: email@example.com
Received: 6 November 2015
Accepted: 16 November 2015
With the ageing population and increased cases of neurodegenerative diseases, there is a crucial need for the development of new nutritional approaches to prevent and delay the onset of cognitive decline. Neuroinflammatory processes contribute to neuronal damage that underpins neurodegenerative disorders. Growing evidence sheds light on the use of dietary n-3 long chain polyunsaturated fatty acids to improve cognitive performances and reduce the neuroinflammatory responses occurring with age and neurodegenerative pathologies. This review will summarise the most recent information related to the impact and mechanisms underlying the neuroinflammatory processes in cognitive disorders. We will also discuss the mechanisms underlying n-3 polyunsaturated fatty acids effect on neuroinflammation and memory decline.
Le développement d’approches nutritionnelles pertinentes pour prévenir et retarder l’apparition du déclin cognitif est un enjeu important, compte tenu du vieillissement de la population et de l’augmentation de l’incidence des maladies neurodégénératives. Les processus neuro-inflammatoires contribuent aux mécanismes neuropathologiques impliqués dans les troubles neurodégénératifs et de la cognition. Des données récentes indiquent l’importance des acides gras polyinsaturés n-3 alimentaires dans le maintien des performances mnésiques et la régulation de la neuroinflammation liée à l’âge ou à la maladie d’Alzheimer. Dans cette revue, seront présentées des données récentes sur les liens existants entre le statut nutritionnel en acides gras polyinsaturés n-3, les processus neuro-inflammatoires et les troubles cognitifs associés, ainsi que les mécanismes qui pourraient être impliqués dans les effets protecteurs de ces acides gras.
Key words: Neuroinflammation / microglia / n-3 polyunsaturated fatty acids / cognitive disorders / Alzheimer disease
Mots clés : Neuroinflammation / microglie / acides gras polyinsaturés n-3 / désordres cognitifs / maladie d’Alzheimer
© Q. Leyrolle et al., published by EDP Sciences, 2016
This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
It is estimated that 35.6 million people worldwide are living with dementia which is predicted to increase to 65.7 million by 2030 and 115.4 million by 2050. Neuroinflammation is recognised for its overall role in Alzheimer Disease (AD) pathology, including the acceleration of neuronal loss and amyloid beta (Aβ) and Tau mysfolding and deposition (Krabbe et al., 2013; Krstic et al., 2012). The majority of AD drug treatments (cholinesterase inhibitors, N-methyl-D-aspartate (NMDA) receptor antagonists) are poorly efficient and do not delay neuronal death. A new potent strategy will be to target neuroinflammatory processes. In this regard, several approaches that directly or indirectly target inflammation are under development (Glass et al., 2010). Recently, much attention has been given to long chain (LC) n-3 polyunsaturated fatty acids (PUFA), eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA), which have potent anti-inflammatory activities, thus interesting for the prevention and treatment of neuroinflammation and cognitive disorders in AD.
Proinflammatory cytokines produced by activated innate immune cells in response to tissue injury, infection or inflammation act on the brain through several pathways (humoral, neural and cellular) (Dantzer et al., 2008). Activation of immune-to-brain communication ultimately induces the production of brain cytokines by activated glial cells, particularly microglia (Dinel et al., 2014; Laye et al., 1994). Neuroinflammation describes the brain inflammatory response involving not only peripheral immune cells influx in the brain but also the discrete response of brain innate immune cells so called microglia. Microglia respond to non sterile stimuli (pathogens such as virus, bacteria, etc) and get activated producing pro and/or anti-inflammatory factors, in particular cytokines but also lipid derived products such as prostaglandins (PG). The microglia response promotes the clearance of pathogens, toxic cellular debris and apoptotic cells and therefore protects the brain. Indeed, a complete blockade of microglial activity exacerbates brain damage in adult and several ischemic injury models (Lalancette-Hebert et al., 2007). Microglia is also activated in the brain associated to ageing, obesity, and neurodegenerative diseases. The cause of microglia activation in neurodegenerative diseases such as AD is rather linked to neuropathological processes such as Aβ synthesis or senescence of microglia cells and reactive oxygen products (Heneka et al., 2015; Laye, 2010).
The sustained expression of inflammatory factors such as proinflammatory cytokines can lead to neurodegeneration. The production of proinflammatory response in the brain is therefore a double-edged sword representing a fine balance between protective and detrimental effects and therefore needs to be tightly regulated. Microglia phenotypes could be crucial in the protective or detrimental role of microglia response toward neurons. Accordingly, whilst activated M1 cells have cytotoxic properties, M2a are involved in repair and regeneration (Perry et al., 2010). In vivo, microglia express proinflammatory cytokines associated with an M1 response (interleukin (IL)-1β, IL-6, IL-12 and tumor necrosis factor (TNF)α) in response to an immune stimulus (Perry et al., 2010), while the anti-inflammatory cytokines IL-10 and IL-4 deactivate the M1 microglial phenotype (Fenn et al., 2012). Microglia senescence, as observed in the ageing brain, impairs microglial cells number, phagocytic activity and increases a production of low-grade proinflammatory cytokines such as IL-1β, IL-6 and TNFα at the expense of anti-inflammatory factors such as IL-10 and IL-4. This state is called inflammaging at the periphery and in the brain. In addition to producing proinflammatory cytokines, senescent microglia also express lipofuscin granules, higher levels of CD86, major histocompatibility complex II (MHC II), toll-like receptors (TLRs) and complement receptor 3 (CD11b) and display a decreased number and complexity of processes as described in activated microglia (Hanisch and Kettenmann, 2007; Tremblay et al., 2011). They also have reduced phagocytic activities of Aβ as demonstrated in aged transgenic mice (Heneka et al., 2010). The mechanisms involved in increased microglia activation in the ageing brain is not fully understood, although the impaired expression of CD200 and CX3CR1, known to be produced by neurons to maintain microglia in the non-activated state in the healthy brain, might be involved (Dilger and Johnson, 2008). In addition, when challenged with either immune stimuli or a stress, aged animals clearly mount an exaggerated neuroinflammatory response, characterized by the overproduction of proinflammatory cytokines (IL-1β, IL-6, TNFα, iNOS) compared to young congeners with a longer duration of activation (Barrientos et al., 2009; Godbout et al., 2005; Sparkman et al., 2005). This phenomenon, first described in a mice model of prion disease is called microglia priming or sensitization (Cunningham et al., 2005). The failure of aged microglia to polarize from a proinflammatory to an anti-inflammatory phenotype supports the detrimental role of primed microglia in neurodegenerative diseases with a self-sustaining and self-amplifying cycle of neurotoxicity. These new knowledge therefore stimulate research aiming at developing drugs targeting the M1 phenotype. Failure to tightly regulate systemic immune activation and/or brain microglial activation leads to significant and prolonged induction of brain cytokines.
Microglia is also activated by insulin resistance developing in the ageing brain. Indeed, brain insulin resistance causes Tau hyper-phosphorylation, increased β amyloid production and plaque-associated microglial-mediated inflammatory responses (De la Monte, 2012). Upregulation of cytosolic phospholipase A2 (cPLA2), which release free fatty acids such as arachidonic acid (AA), has also been reported in neurodegenerative diseases such as AD (Sundaram et al., 2013). AA metabolisation by cycloxygenases (COX) and lipoxygenases (LOX) into PG, leukotrienes, thromboxanes (TX) and lipoxins further triggers the neuroinflammatory response (Ong et al., 2015).
The underlying mechanisms of neuronal degeneration associated with cognitive decline remain elusive, although it is thought that several cellular and molecular events are involved which are sensitive to oxidative stress and chronic neuroinflammation. Indeed, chronic cytokines production has been proposed to participate in cognitive decline through processes related to neuroinflammation, neurodegeneration, structural remodelling and impaired neurotransmission (Capuron and Miller, 2011; Delpech et al., 2015a; Laye, 2010). In particular, the activation of microglia leads to de novo production of proinflammatory cytokines (i.e. IL-1β, IL-6 and TNFα), chemokines, nitric oxide (NO), eicosanoids (i.e. PGE2) and reactive oxygen species (ROS) (Barrientos et al., 2015; Vauzour, 2012). For example, increased level of IL-1β elevates the production of ROS, which in turn, activates mitogen-activated protein (MAP) kinases such as c-Jun N-terminal kinase (JNK) and p38, resulting in cell damage and cell death therefore impairing the long-term potentiation (LTP) and leading to cognitive decline. In addition, the excessive production of pro-inflammatory cytokines such as TNFα and IL-1β has been reported to result in glutamate cytotoxicity by directly stimulating NMDA receptors while inhibiting gamma-amino-butyric acid (GABA)-A receptors (Barrientos et al., 2015; Olmos and Llado, 2014).
Another mechanism by which cytokines may impair synaptic plasticity (Delpech et al., 2015b) is their capacity to induce the synthesis of indoleamine 2,3-dioxygenase (IDO), a rate-limiting enzyme degrading tryptophan along the kynurenine pathway, in activated microglia. Although cytokine-induced activation of IDO is usually beneficial to the host (Harrington et al., 2008), sustained brain IDO activation can also be deleterious by negatively impacting the monoaminergic neurotransmission (e.g. serotonin, dopamine) and neuronal survival (Capuron and Miller, 2011; Dantzer et al., 2008). Indeed, increased brain or cerebrospinal fluid concentrations of kynurenine and its neurotoxic metabolites have been reported in several neurodegenerative and psychiatric disorders (Campbell et al., 2014; Capuron et al., 2011) suggesting that IDO activation may lead to both functional and structural alterations in the brain. Consistent with this statement, activation of the kynurenine pathway has been recently reported to affect human neurogenesis in the hippocampal formation (Zunszain et al., 2012), an important brain structure involved in cognitive functions and an important site for IDO production (Andre et al., 2008; Frenois et al., 2007). In addition, pharmacological or genetic inhibition of IDO activity prevents induction of cognitive impairments (reviewed in (Castanon et al., 2014).
Recently, the role of guanosine triphosphate cyclohydrolase I (GTP-CH1) in the cognitive effect of chronic inflammation has also been revealed in elderly (Capuron and Miller, 2011). GTP-CH1 is the rate-limiting enzyme of GTP conversion into 7,8-dihydroneopterin (BH2), which leads to the production of neopterin at the expense of tetrahydrobiopterin (BH4) (Oxenkrug, 2011). BH4 is a cofactor of aromatic amino acid hydroxylase and therefore plays a fundamental role in dopamine synthesis (Neurauter et al., 2008). Cytokines-induced GTP-CH1 activation, classically assessed by measuring increased production of neopterin, is therefore able to impair the dopaminergic neurotransmission which is known to be involved in mood disorders and cognitive dysfunctions, including in conditions of chronic immune stimulation (Capuron et al., 2011).
As a result of the lack of effectiveness of current treatments for cognitive disorders, a lot of effort has been invested to enhance the search for new therapeutic targets. Based on the results obtained in patients taking anti-inflammatory drugs, a new possibility has been opened studying the association of inflammatory processes and brain pathophysiology. An important strategy to prevent brain impairment is based on dietary changes and nutritional supplements, functional foods and nutraceuticals. In this regard, a substantial amount of recent evidence suggests that many food components and in particular n-3 PUFA, could be good candidates to modulate inflammation both acutely and chronically. LC n-3 PUFA modulate the inflammatory processes by acting at the immune system level through the regulation of inflammatory gene expression, especially cytokines and chemokines, the decrease of inflammatory PG and eicosanoids and the induction of pro-resolutive factors, resolvins and protectins that are involved in the resolution of inflammation (Calder, 2013; Serhan, 2007; Serhan et al., 2007). LC n-3 PUFA anti-inflammatory effects are thought to require their incorporation into plasma membranes of target tissues, however they have short-term effect as they are rapidly metabolized into bioactive products. In particular, EPA, DHA and their bioactive mediators have potent anti-inflammatory and pro-resolving properties in the periphery (Serhan and Chiang, 2013) and in the brain (Bazinet and Laye, 2014; Laye, 2010; Orr and Bazinet, 2008; Rapoport, 2008). Loss of these regulatory processes can result in excessive, inappropriate or on-going inflammation that can cause irreparable damage to host tissues, including the brain. EPA is a substrate for the COX, LOX and cytochrome P450 enzymes that produce 3-series eicosanoids (PG and TX) and 5-series leucotrienes that are increased in macrophages or neutrophils enriched in EPA and DHA by dietary means (Calder and Grimble, 2002; Yates et al., 2014). In addition, other anti-inflammatory and pro-resolving derivates so-called resolvins, protectins and maresins are produced from EPA and DHA from the COX and LOX pathways. Resolvin E1 (RvE1), RvE2 and RvE3 are produced from EPA and RvD1, RvD2 and RvD5 are biosynthesized from DHA (reviewed in Serhan, 2007; Serhan et al., 2011). When produced in the brain, protectins are referred to as neuroprotectins (Bazan, 2012).
The cellular concentrations of LC n-3 and n-6 PUFA and their metabolites are determined by their relative dietary intake. Increased dietary intake of LC n-3 PUFA has been shown to significantly alter DHA levels in the brain (Freund Levi et al., 2014) suggesting that DHA and EPA dietary supplementation could be used to directly influence neuroinflammatory pathways (Bazinet and Laye, 2014). DHA entry in the brain is still a matter of debate. Non esterified DHA freely enters the brain (Bazinet and Laye, 2014; Song et al., 2010) and recently, an orphan receptor, the major facilitator superfamily domain-containing protein 2a (Mfsd2a) has been described as important to transport DHA through the BBB (Nguyen et al., 2014). In retinal cells, adiponectin receptor 1 is key for DHA uptake and retention (Rice et al., 2015). Once in the brain, DHA exerts anti-inflammatory/pro-resolutive activities through several action modes briefly described below. We will focus on the effect of LC n-3 PUFA on neuroinflammatory processes, especially DHA as this LC n-3 PUFA accumulates in the brain, while EPA does not.
At the periphery, inflammation is tightly regulated to be quickly resolved. The control and resolution of inflammation is due to the activation of several negative feedback mechanisms: secretion of anti-inflammatory cytokines, inhibition of pro-inflammatory signalling cascades, shedding of receptors acting as decoy targets for inflammatory mediators, glucocorticoids and activation of regulatory cells. More recently, pro-resolving lipid mediators have been identified as novel key regulators of the resolution of inflammation. Resolution is an active mechanisms allowing tissues to return to homeostasis in particular through pushing back invading neutrophils from the inflamed tissue by new produced factors (Serhan, 2007). Indeed, the LC n-3 PUFA modulate the inflammatory processes by acting at the immune system level through the regulation of inflammatory gene expression, especially cytokines and chemokines, the decrease of inflammatory PG and eicosanoids and the induction of proresolutive factors, resolvins and protectins that are involved in the resolution of inflammation (Calder, 2013; Serhan et al., 2007; Serhan and Chiang, 2013). LC n-3 PUFA anti-inflammatory effects are thought to require their incorporation into plasma membranes of target tissues, however they have short term effect as they are metabolized in bioactive products quite quickly. In particular EPA, DHA and their bioactive mediators have potent anti-inflammatory and pro-resolving properties in the periphery (Serhan and Chiang, 2013) and in the brain (Bazinet and Laye, 2014; Laye, 2010; Orr and Bazinet, 2008; Rapoport, 2008). Loss of these regulatory processes can result in excessive, inappropriate or on-going inflammation that can cause irreparable damage to host tissues, including the brain. Several reports in humans highlight that higher dietary intake or blood/brain level of EPA and/or DHA are correlated with lower risk of developing brain diseases with an inflammatory component including AD and PD recently reviewed in (Bazinet and Laye, 2014).
EPA is a substrate for the COX, LOX and cytochrome P450 enzymes that produce 3-series eicosanoids (PG and TX) and 5-series leucotrienes (LT) that are increased in macrophages or neutrophils enriched in EPA and DHA by dietary means (Calder and Grimble, 2002; Yates et al., 2014). As the enzymatic pathway used to convert EPA into the 3 and 5 series derivates is the same than the one used to convert arachidonic acid (AA), a n-6 PUFA, into series 2 derivates, the higher level of EPA allow to produce more 3 series derivates that are less proinflammatory. Thus, EPA results in decreased production of proinflammatory eicosanoids from AA and increased production of weaker proinflammatory eicosanoids. In addition, other anti-inflammatory and pro-resolving derivates so-called resolvins, protectins and maresins are produced from EPA and DHA from the COX and LOX pathways. Resolvin E1 (RvE1), RvE2 and RvE3 are produced from EPA and RvD1, RvD2 and RvD5 are biosynthesized from DHA (reviewed in Serhan, 2007; Serhan et al., 2011). When produced in the brain, protectins are referred to as neuroprotectins (Bazan, 2012). Importantly, resolvin synthesis is increased in the blood or peripheral tissues of both humans and laboratory rodent with enriched levels of EPA and DHA by dietary means (Calder, 2015). The anti-inflammatory activity of these compounds is linked to the inhibition of the synthesis of proinflammatory cytokines such as IL-1β and TNFα and the inhibition of trans-endothelial migration of neutrophils into tissues, preventing the infiltration of these cells in inflamed tissues therefore protecting from excessive inflammation (Ariel and Serhan, 2007; Calder, 2015). Some of the biological activities of resolvins are mediated by specific G-protein coupled receptors. Indeed, RvD1 activates lipoxin A4 receptor/formyl peptide receptor 2 (ALX/FPR2) and orphan receptor G protein coupling receptor 32 (GPR32) to limit leukocyte infiltration in tissues and attenuate the production of proinflammatory cytokines (Fredman et al., 2014; Wang et al., 2014). Interestingly, RvD1 promotes the synthesis of pro-resolvin miRNAs and elicits macrophage polarization toward an M2-like phenotype (Pierdomenico et al., 2015).
LC PUFA cannot be synthesized by vertebrates and must be obtained from diet. Therefore, the cellular concentrations of LC n-3 and n-6 PUFA, and their relative derived bioactive products are determined by their relative dietary intake. Increased dietary intake of LC n-3 PUFA has been shown to significantly alter DHA levels in the brain (Freund Levi et al., 2014) suggesting that DHA and EPA dietary supplementation could be used to directly influence neuroinflammatory pathways (Bazinet and Laye, 2014). DHA entry in the brain is still a matter of debate. Non esterified DHA freely entries the brain (Bazinet and Laye, 2014; Song et al., 2010). Recently, an orphan receptor, the major facilitator superfamily domain-containing protein 2a (Mfsd2a) has been described as important to transport DHA through the BBB (Nguyen et al., 2014). Once in the brain, DHA exerts anti-inflammatory/proresolutive activities through several action modes briefly described below. However, poor studies studied in humans the effect of LC n-3 PUFA supplementation on neuroinflammation or microglia activity in vivo.
Higher dietary intakes of DHA are correlated with lower risk of developing several neurodegenerative and neuropsychiatric diseases that are associated with inflammatory component (AD, depression, etc.) thus it was hypothesized that one mechanism may be via anti-inflammatory signalling in the brain (Bazinet and Laye, 2014; Laye, 2010) Epidemiological studies have provided more consistent support for n-3 PUFA’s anti-inflammatory properties than randomized controlled trials (RCTs) (Sijben and Calder, 2007). Indeed, several epidemiological and observational studies report that a higher level of blood n-3 PUFAs is associated with lower proinflammatory cytokine production (Alfano et al., 2012; Farzaneh-Far et al., 2009; Ferrucci et al., 2006; Kiecolt-Glaser et al., 2007, 2011). In a cohort of elderly subjects, depressive individuals with an elevated plasma n-6/n-3 ratio were found to exhibit higher levels of the proinflammatory cytokine TNFα and of IL-6 (Kiecolt-Glaser et al., 2007). F2-isoprostane, an oxidative marker and telomere length an indicator of immune cell ageing, are decreased in the blood of subjects supplemented with EPA/DHA (Kiecolt-Glaser et al., 2013). Additionally, LC n-3 PUFA supplementation in elderly subjects reduced the levels of inflammatory cytokines produced by blood leukocytes stimulated in vitro (Meydani et al., 1991). The production of PGE2 by monocytes is inversely correlated to the EPA content of leukocytes obtained from aged subjects after the consumption of dietary complements containing different doses of EPA (Rees et al., 2006). However, even if most of randomized trials with LC n-3 PUFAs have reported consistent decreased inflammation in groups with high baseline inflammation (stressed students, elderly, diabetics, and hypertriglyceridemic subjects), results are mixed (Fritsche, 2006). Indeed, DHA/EPA dietary supplementation in healthy subjects blunted the endocrine stress response and the increase in body temperature, with or without impact on cytokine production after bacterial endotoxin administration (Ferguson et al., 2014; Michaeli et al., 2007). AD patients supplemented with a DHA-rich diet display reduced release of proinflammatory cytokines (IL-1β, IL-6, GM-CSF) from stimulated peripheral blood mononuclear cells (Vedin et al., 2008). In addition, students with DHA/EPA supplementation show a decreased anxiety and proinflammatory cytokines production only in ex vivo stimulated immune cells but not in the plasma (Kiecolt-Glaser et al., 2011). However, decreased plasma cytokines level was observed in students with the higher increase of LC n-3 PUFA after supplementation, reinforcing the necessity in RCT of evaluate both basal level of LC n-3/n-6 PUFA before and after dietary interventions. A potential explanation of conflicting results from randomised controlled trials might be that some condition-specific clinical end points are more sensitive markers to LC n-3 PUFA treatment than immune markers. For instance, a LC n-3 PUFA-enriched diet (Souvenaid® formulation) revealed improved cognitive decline in mild AD patients without taking any AD drug, by influencing synaptic plasticity along with cognitive tasks (Scheltens et al., 2012). Additionally, as lifestyle habits impact on cognition and the onset of dementia, the efficacy of a LC n-3 PUFA enriched diet on neuroinflammatory markers might be revealed if included in a multidomain intervention trial. The Finnish geriatric intervention study to prevent cognitive impairment and disability (FINGER) study is the first long-term randomised controlled trial showing a beneficial impact on cognition in at-risk older individuals of a multiple intervention (nutritional guidance, exercise, cognitive training and social activity) (Ngandu et al., 2015). The development of such strategies points out the importance of assessing the subject’s lifestyle habits in particular from mid-life (Fratiglioni et al., 2004, 2007).
Whether decreased brain DHA level through dietary means is proinflammatory in absence of proinflammatory stimulus has been poorly studied in animal models. In vivo, chronic dietary n-3 PUFA deficiency significantly increased the production and release of IL-6 and TNFα in the blood (McNamara et al., 2010) while it was not the case in adult and aged mice brain (Delpech et al., 2015a; Mingam et al., 2008; Moranis et al., 2012). However, DHA decrease in the brain during post-natal period strongly affects microglia activity (Madore et al., 2014). On the opposite, the expression of brain proinflammatory cytokines following systemic LPS administration (Delpech et al., 2015a; Mingam et al., 2008), brain ischemia-reperfusion (Lalancette-Hebert et al., 2011) or spinal cord injury (Huang et al., 2007) is reduced in the brain of rodents with higher level of DHA by genetic or dietary means. Short-term exposure to dietary EPA reduced IL-1-induced spatial memory deficit and anxiolytic behavior (Song et al., 2004, 2008) and improved LPS and Aβ-induced inhibition of LTP in both adult and aged rats (Minogue et al., 2007). Furthermore, DHA and NPD1 infusion in the brain is acutely protective toward brain cytokine production and microglia activation (Lukiw et al., 2005; Orr et al., 2013). In addition, DHA increase in the brain protects from the effect of bacterial endotoxin-induced synaptic plasticity impairment and ageing (Delpech et al., 2015a, 2015c; Labrousse et al., 2012).
Proper neuronal membrane lipid composition is crucial to maintain neuronal signalling. Neuronal membranes, which are highly enriched in DHA (Bazan et al., 2011), are susceptible to oxidative damage and metabolic perturbations. As most receptors are embedded, damage to the membrane would disrupt all forms of neuronal communication (Gomez-Pinilla et al., 2008). With ageing, lipid composition and fat deposition distribution are disturbed in the brain, most likely due to decreased liver peroxisomal β-oxidation (Yang et al., 2014; Zamzow et al., 2014), which is responsible for specific fatty acids synthesis such as DHA (Ferdinandusse et al., 2001). In addition, along with the decreased level and activity of the enzyme delta 6-desaturase (Yehuda et al., 2005), the higher cholesterol content in the ageing neuronal membrane decreases membrane fluidity of the BBB (Yehuda et al., 2002). Both in vivo and in vitro studies have reported anti-inflammatory activities of DHA in the brain especially in microglia (Laye, 2010; Orr and Bazinet, 2008). At the cellular level, brain DHA modulates several proinflammatory signalling pathways in microglia such as TLR signalling and nucleotide-binding oligomerization domain protein (NOD) signalling (De Smedt-Peyrusse et al., 2008; Liu et al., 2012), inhibits JUNK (Ma et al., 2009), and reduces or blocks NF-kB signalling (De Smedt-Peyrusse et al., 2008; Orr et al., 2013). The inhibitory effect of DHA on proinflammatory signalling pathway could be mediated by both non-genomic and genomic effect. Indeed, DHA influences membrane composition of microglial cells and the TLR4 positioning, decreasing the binding of its ligand LPS (De Smedt-Peyrusse et al., 2008). DHA also impairs the phospholipid raft assembly of EPA and DHA in the plasma membrane (Rockett et al., 2011; Ruth et al., 2009). In addition, genomic effect of DHA has been reported thanks to its effect on specific receptors either located at the membrane such as GPR120 or GPR40 and/or the regulation of the peroxisome proliferator activated receptor (PPARγ) (Calder, 2013). The anti-inflammatory activity of DHA could also derive from its direct effect on invading macrophages or microglia. Both in vitro and in vivo data highlight that DHA blocks invading macrophages and microglia activation and the signalling pathway (NF-kB) in the brain and spinal cord of several inflammatory rodents models (De Smedt-Peyrusse et al., 2008; Figueroa et al., 2012; Lim et al., 2013; Lu et al., 2013). Recent data highlight that in vitro DHA has not only anti-inflammatory activity but also promotes microglia to a M2 phenotype with increased Aβ42 phagocytosis (Hjorth et al., 2013).
In the brain, LC n-3 PUFA could also yield protective influence indirectly, through the synthesis of bioactive derivates with pro-resolutive activities. Indeed, several in vitro studies performed on microglia show that several LC n-3 PUFA pro-resolving derivatives have potent effects. As an example, RvD1 triggers anti-inflammatory activities and potentiates IL-4-induced expression of M2 markers in microglial cells and the signaling pathways involved in these processes, in particular the PPARγ signalling pathways (Li et al., 2014; Odusanwo et al., 2012; Wang et al., 2014). In addition, RvD1 inhibits the activation of several proinflammatory signalling pathways, including NFkB and MAPK in microglia cells which express RvD1 receptors ALX (Xu et al., 2013). Another important mediator of anti-inflammatory activity of DHA is NPD1 (Bazan, 2006, 2012). This DHA derivative inhibits leukocyte infiltration, COX-2 expression, and NFκB activation in vivo and in vitro (Marcheselli et al., 2010). In addition, aspirine-triggered NPD1 (AT-NPD1), recently discovered as a new potent neuroprotective derivative of DHA, could also exert strong anti-inflammatory and pro-resolutive activities (Bazan et al., 2012).
In the ageing brain, microglial activation, production of proinflammatory cytokines such as IL-1β and alterations in hippocampal LTP with age are attenuated by EPA (Lynch et al., 2003, 2007). A 2-month fish-oil dietary supply increases DHA in the brain, prevented proinflammatory cytokines expression and astrocytes morphology changes in the hippocampus and restored spatial memory deficits and Fos-associated activation in the hippocampus of aged mice (Labrousse et al., 2012). To the extent that the level of peripheral cytokines reflects that of cytokines in the brain, these results suggest that dietary n-3 PUFAs modulate neuroinflammation and associated neurobehavioural effects in elderly individuals. However, the direct effect of DHA on the brain immune system is difficult to ascertain since primary injury in these animal models of neuroinflammation was also improved. Chronic neuroinflammation in the brain of patients with AD could indicate that the resolution of inflammation is dysfunctional. To support this notion, while proinflammatory stimuli such as LPS promoted resolvin pathways activation in microglia, Aβ42 had an opposite or insignificant effect suggesting that pro-resolutive pathways are impaired in AD (Zhu et al., 2015). This is further substantiated by the observation that the lipoxin A4 (LXA4) level is decreased in postmortem brain tissue and cerebrospinal fluid samples from AD patients (Wang et al., 2015b). Very recently, it was shown that upon Aβ40 exposure, peripheral blood mononuclear cells from AD patients secreted less LXA4 and RvD1 together with the disease progression. Importantly, dietary supplementation of DHA prevented this reduction (Wang et al., 2015a), suggesting that long chain n-3 PUFAs protect from the Alzheimer-associated inflammation through the promotion of pro-resolving signaling. Interestingly, LOX and LTB4 expression increases while LXA4 decreases in the brain of aged and AD mice models (Dunn et al., 2015).
Recent data show that 12 and 5-LOX are widely expressed in the brain where it mainly localizes in neuronal cells. In vivo overexpression of 5-LOX increases phosphorylation of specific Tau epitopes, and neuronal cells transfected with 5-LOX show a significant increase in tau phosphorylation even when their ability to generate Aβ is completely blocked, suggesting that the effect on tau is independent from Aβ (Chu et al., 2012). Interestingly, Tau-mice treated with zileuton (a potent 5-LOX inhibitor) displayed a significant improvement in memory and synaptic function together with a decreased tau phosphorylation level (Chu and Pratico, 2013; Giannopoulos et al., 2014). The use of PD146176, a specific 12/15 LOX inhibitor, also improved memory deficits and decreased Aβ plaques and neurofibrillary tangles in a genetic mice model of AD (Chu et al., 2015). All together, these data suggest the importance of using DHA and/or its mediator to target neuroinflammatory processes in the management of neurodegenerative diseases. This new therapeutic strategy is of particular importance since the target of proinflammatory pathways with COX-2 inhibitors is puzzling as (1) they poorly cross the BBB, (2) some of AA derivatives dependent on COX-2 are proresolutive and (3) COX-2 inhibitors are poorly efficient in AD (Aid and Bosetti, 2007, 2011; McGeer and McGeer, 2007).
Chronic neuroinflammation, demonstrated by the activation of microglia and astrocytes as well as the release of reactive oxygen species and cytokines, has a considerable interest in cognitive disorders, and is a target site for developing for prevention and treatment of neurodegenerative diseases. In this regard, n-3 PUFAs are an interesting dietary strategy to limit dementia. A better understanding of the effects of n-3 PUFAs and their derivatives in microglia are therefore warranted. Nonetheless, it is worth noting that it is not clear whether the n-3 PUFAs derivatives with anti-inflammatory activity access the brain to interact directly with microglia. While it is biologically plausible that peripheral inflammatory modulation may reflect brain health, further human studies are required to elucidate whether dietary n-3 PUFAs target microglia. The use of imaging techniques like positron emission tomography (PET) imaging to measure in vivo changes in microglia activation (Cagnin et al., 2007) would be of high benefit to decipher this important question.
The authors declare no financial or personal conflict of interest.
QL is a recipient of Paris Ile de France stipend. AN and SL are supported by INRA, Bordeaux University, Région Aquitaine.
- Aid S, Bosetti F. 2007. Gene expression of cyclooxygenase-1 and Ca2+-independent phospholipase A2 is altered in rat hippocampus during normal aging. Brain Res. Bull. 73: 108–113. [CrossRef] [PubMed] [Google Scholar]
- Aid S, Bosetti F. 2011. Targeting cyclooxygenases-1 and -2 in neuroinflammation: Therapeutic implications. Biochimie 93: 46–51. [CrossRef] [PubMed] [Google Scholar]
- Alfano CM, Imayama I, Neuhouser ML, et al. 2012. Fatigue, inflammation, and omega-3 and omega-6 fatty acid intake among breast cancer survivors. J. Clin. Oncol. 30: 1280–1287. [CrossRef] [PubMed] [Google Scholar]
- Andre C, O’Connor JC, Kelley KW, Lestage J, Dantzer R, Castanon, N. 2008. Spatio-temporal differences in the profile of murine brain expression of proinflammatory cytokines and indoleamine 2,3-dioxygenase in response to peripheral lipopolysaccharide administration. J. Neuroimmunol. 200: 90–99. [CrossRef] [PubMed] [Google Scholar]
- Ariel A, Serhan CN. 2007. Resolvins and protectins in the termination program of acute inflammation. Trends Immunol. 28: 176–183. [CrossRef] [Google Scholar]
- Barrientos RM, Frank MG, Hein AM, et al. 2009. Time course of hippocampal IL-1 beta and memory consolidation impairments in aging rats following peripheral infection. Brain Behav. Immun. 23: 46–54. [CrossRef] [PubMed] [Google Scholar]
- Barrientos RM., Kitt MM, Watkins LR., Maier SF. 2015. Neuroinflammation in the normal aging hippocampus. Neuroscience 309: 84–99. [CrossRef] [PubMed] [Google Scholar]
- Bazan NG. 2006. Cell survival matters: docosahexaenoic acid signaling, neuroprotection and photoreceptors. Trends Neurosci. 29: 263–271. [CrossRef] [Google Scholar]
- Bazan NG. 2007. Omega-3 fatty acids, pro-inflammatory signaling and neuroprotection. Curr. Opin. Clin. Nutr. Metab. Care 10: 136–141. [Google Scholar]
- Bazan NG. 2012. Neuroinflammation and proteostasis are modulated by endogenously biosynthesized neuroprotectin D1. Mol. Neurobiol. 46: 221–226. [CrossRef] [PubMed] [Google Scholar]
- Bazan NG, Eady TN, Khoutorova L, et al. 2012. Novel aspirin-triggered neuroprotectin D1 attenuates cerebral ischemic injury after experimental stroke. Exp. Neurol 236: 122–130. [CrossRef] [PubMed] [Google Scholar]
- Bazan NG, Molina MF, Gordon WC. 2011. Docosahexaenoic acid signalolipidomics in nutrition: significance in aging, neuroinflammation, macular degeneration, Alzheimer’s, and other neurodegenerative diseases. Annu. Rev. Nutr. 31: 321–351. [Google Scholar]
- Bazinet RP, Laye S. 2014. Polyunsaturated fatty acids and their metabolites in brain function and disease. Nat. Rev. Neurosci. 15: 771–785. [Google Scholar]
- Cagnin A, Kassiou M, Meikle SR, Banati RB. 2007. Positron emission tomography imaging of neuroinflammation. Neurotherapeutics 4: 443–452. [CrossRef] [Google Scholar]
- Calder PC. 2013. n-3 fatty acids, inflammation and immunity: new mechanisms to explain old actions. Proc. Nutr. Soc. 72: 326–336. [Google Scholar]
- Calder PC. 2015. Marine omega-3 fatty acids and inflammatory processes: Effects, mechanisms and clinical relevance. Biochim. Biophys. Acta 1851: 469–484. [Google Scholar]
- Calder PC, Grimble RF. 2002. Polyunsaturated fatty acids, inflammation and immunity. Eur. J. Clin. Nutr. 56: S14–19. [CrossRef] [PubMed] [Google Scholar]
- Campbell BM, Charych E, Lee AW, Moller T. 2014. Kynurenines in CNS disease: regulation by inflammatory cytokines. Front. Neurosci. 8: 12. [CrossRef] [PubMed] [Google Scholar]
- Capuron L, Miller AH. 2011. Immune system to brain signaling: neuropsychopharmacological implications. Pharmacol. Ther. 130: 226–238. [Google Scholar]
- Capuron L, Schroecksnadel S, Feart C, Aubert A, Higueret D, Barberger-Gateau P, Laye S, Fuchs D, 2011. Chronic low-grade inflammation in elderly persons is associated with altered tryptophan and tyrosine metabolism: role in neuropsychiatric symptoms. Biol. Psychiatry. 70: 175–182. [CrossRef] [PubMed] [Google Scholar]
- Castanon N, Lasselin J, Capuron L. 2014. Neuropsychiatric comorbidity in obesity: role of inflammatory processes. Front. Endocrinol. (Lausanne) 5: 74. [CrossRef] [Google Scholar]
- Chu J, Pratico D. 2013. 5-Lipoxygenase pharmacological blockade decreases tau phosphorylation in vivo: involvement of the cyclin-dependent kinase-5. Neurobiol. Aging. 34: 1549–1554. [CrossRef] [PubMed] [Google Scholar]
- Chu J, Giannopoulos PF, Ceballos-Diaz C, Golde TE, Pratico D. 2012. 5-Lipoxygenase gene transfer worsens memory, amyloid, and tau brain pathologies in a mouse model of Alzheimer disease. Ann. Neurol. 72: 442–454. [CrossRef] [PubMed] [Google Scholar]
- Chu J, Li JG, Giannopoulos PF, Blass BE, Childers W, Abou-Gharbia M, Pratico D. 2015. Pharmacologic blockade of 12/15-lipoxygenase ameliorates memory deficits, Abeta and tau neuropathology in the triple-transgenic mice. Mol. Psychiatry. 20: 1329–38. [CrossRef] [PubMed] [Google Scholar]
- Cunningham C, Wilcockson DC, Campion S, Lunnon K, Perry VH. 2005. Central and systemic endotoxin challenges exacerbate the local inflammatory response and increase neuronal death during chronic neurodegeneration. J. Neurosci. 25: 9275–9284. [CrossRef] [PubMed] [Google Scholar]
- Dantzer R, O’Connor JC, Freund GG, Johnson RW, Kelley KW. 2008. From inflammation to sickness and depression: when the immune system subjugates the brain. Nat. Rev. Neurosci. 9: 46–56. [Google Scholar]
- De la Monte SM. 2012. Brain insulin resistance and deficiency as therapeutic targets in Alzheimer’s disease. Curr. Alzheimer. Res. 9: 35–66. [CrossRef] [PubMed] [Google Scholar]
- De Smedt-Peyrusse V, Sargueil F, Moranis A, Harizi H, et al. 2008. Docosahexaenoic acid prevents lipopolysaccharide-induced cytokine production in microglial cells by inhibiting lipopolysaccharide receptor presentation but not its membrane subdomain localization. J. Neurochem. 105: 296–307. [CrossRef] [PubMed] [Google Scholar]
- Delpech JC, Madore C, Joffre C, et al. 2015a. Transgenic increase in n-3/n-6 fatty acid ratio protects against cognitive deficits induced by an immune challenge through decrease of neuroinflammation. Neuropsychopharmacology 40: 525–536. [CrossRef] [PubMed] [Google Scholar]
- Delpech JC, Saucisse N, Parkes SL, et al. 2015b. Microglial activation enhances associative taste memory through purinergic modulation of glutamatergic neurotransmission. J. Neurosci. 35: 3022–3033. [CrossRef] [PubMed] [Google Scholar]
- Delpech JC, Thomazeau A, Madore C, et al. 2015c. Dietary n-3 PUFAs Deficiency Increases Vulnerability to Inflammation-Induced Spatial Memory Impairment. Neuropsychopharmacology 40: 2774–87. [CrossRef] [PubMed] [Google Scholar]
- Dilger RN, Johnson RW. 2008. Aging, microglial cell priming, and the discordant central inflammatory response to signals from the peripheral immune system. J. Leukoc. Biol. 84: 932–939. [CrossRef] [PubMed] [Google Scholar]
- Dinel AL, Andre C, Aubert A, Ferreira G, Laye S, Castanon N. 2014. Lipopolysaccharide-induced brain activation of the indoleamine 2,3-dioxygenase and depressive-like behavior are impaired in a mouse model of metabolic syndrome. Psychoneuroendocrinology 40: 48–59. [CrossRef] [PubMed] [Google Scholar]
- Dunn HC, Ager RR, Baglietto-Vargas D, et al. 2015. Restoration of lipoxin A4 signaling reduces Alzheimer’s disease-like pathology in the 3xTg-AD mouse model. J. Alzheimers Dis. 43: 893–903. [PubMed] [Google Scholar]
- Farzaneh-Far R, Harris WS, Garg S, Na B, Whooley MA. 2009. Inverse association of erythrocyte n-3 fatty acid levels with inflammatory biomarkers in patients with stable coronary artery disease: The Heart and Soul Study. Atherosclerosis 205: 538–543. [CrossRef] [PubMed] [Google Scholar]
- Fenn AM, Henry CJ, Huang Y, Dugan A, Godbout JP. 2012. Lipopolysaccharide-induced interleukin (IL)-4 receptor-alpha expression and corresponding sensitivity to the M2 promoting effects of IL-4 are impaired in microglia of aged mice. Brain Behav. Immun. 26: 766–777. [CrossRef] [PubMed] [Google Scholar]
- Ferdinandusse S, Denis S, Mooijer PA, et al. 2001. Identification of the peroxisomal beta-oxidation enzymes involved in the biosynthesis of docosahexaenoic acid. J. Lipid. Res. 42: 1987–1995. [PubMed] [Google Scholar]
- Ferguson JF, Mulvey CK, Patel PN, et al. 2014. Omega-3 PUFA supplementation and the response to evoked endotoxemia in healthy volunteers. Mol. Nutr. Food. Res. 58: 601–613. [CrossRef] [PubMed] [Google Scholar]
- Ferrucci L, Cherubini A, Bandinelli S, et al. 2006. Relationship of plasma polyunsaturated fatty acids to circulating inflammatory markers. J. Clin. Endocrinol. Metab. 91: 439–446. [CrossRef] [PubMed] [Google Scholar]
- Figueroa JD, Cordero K, Baldeosingh K, et al. 2012. Docosahexaenoic acid pretreatment confers protection and functional improvements after acute spinal cord injury in adult rats. J. Neurotrauma. 29: 551–566. [CrossRef] [PubMed] [Google Scholar]
- Fratiglioni L, Paillard-Borg S, Winbla B. 2004. An active and socially integrated lifestyle in late life might protect against dementia. Lancet Neurol. 3: 343–5. [CrossRef] [PubMed] [Google Scholar]
- Fratiglioni L, Winblad B, von Strauss E. 2007. Prevention of Alzheimer’s disease and dementia. Major findings from the Kungsholmen Project. Physiol. Behav. 92: 98–104. [CrossRef] [PubMed] [Google Scholar]
- Fredman G, Ozcan L, Spolitu S, Hellmann J, Spite M, Backs J, Tabas I. 2014. Resolvin D1 limits 5-lipoxygenase nuclear localization and leukotriene B4 synthesis by inhibiting a calcium-activated kinase pathway. Proc. Natl. Acad. Sci. USA 111: 14530–14535. [CrossRef] [Google Scholar]
- Frenois F, Moreau M, O’Connor J, et al. 2007. Lipopolysaccharide induces delayed FosB/DeltaFosB immunostaining within the mouse extended amygdala, hippocampus and hypothalamus, that parallel the expression of depressive-like behavior. Psychoneuroendocrinology 32: 516–531. [CrossRef] [PubMed] [Google Scholar]
- Freund Levi Y, Vedin I, Cederholm T, et al. 2014. Transfer of omega-3 fatty acids across the blood-brain barrier after dietary supplementation with a docosahexaenoic acid-rich omega-3 fatty acid preparation in patients with Alzheimer’s disease: the OmegAD study. J. Intern. Med. 275: 428–436. [CrossRef] [PubMed] [Google Scholar]
- Fritsche K. 2006. Fatty acids as modulators of the immune response. Annu. Rev. Nutr. 26: 45–73. [CrossRef] [PubMed] [Google Scholar]
- Giannopoulos PF, Chu J, Joshi YB, Sperow M, Li JG, Kirby LG, Pratico D. 2014. Gene knockout of 5-lipoxygenase rescues synaptic dysfunction and improves memory in the triple-transgenic model of Alzheimer’s disease. Mol. Psychiatry 19: 511–518. [CrossRef] [PubMed] [Google Scholar]
- Glass CK, Saijo K, Winner B, Marchetto MC, Gage FH. 2010. Mechanisms underlying inflammation in neurodegeneration. Cell 140: 918–934. [CrossRef] [PubMed] [Google Scholar]
- Godbout JP, Chen J, Abraham J, et al. 2005. Exaggerated neuroinflammation and sickness behavior in aged mice following activation of the peripheral innate immune system. Faseb. J. 19: 1329–1331. [CrossRef] [PubMed] [Google Scholar]
- Gómez-Pinilla F. 2008. Brain foods: the effects of nutrients on brain function. Nat. Rev. Neurosci. 9: 568–78. [CrossRef] [PubMed] [Google Scholar]
- Hanisch UK, Kettenmann H. 2007. Microglia: active sensor and versatile effector cells in the normal and pathologic brain. Nat. Neurosci. 10: 1387–1394. [CrossRef] [PubMed] [Google Scholar]
- Harrington L, Srikanth CV, Antony R, et al. 2008. Deficiency of indoleamine 2,3-dioxygenase enhances commensal-induced antibody responses and protects against Citrobacter rodentium-induced colitis. Infect. Immun. 76: 3045–3053. [CrossRef] [PubMed] [Google Scholar]
- Heneka MT, O’Banion MK, Terwel D, Kummer MP. 2010. Neuroinflammatory processes in Alzheimer’s disease. J. Neural. Transm. 117: 919–947. [CrossRef] [PubMed] [Google Scholar]
- Heneka MT, Carson MJ, El Khoury J, et al. 2015. Neuroinflammation in Alzheimer’s disease. Lancet Neurol. 14: 388–405. [CrossRef] [PubMed] [Google Scholar]
- Hjorth E, Zhu M, Toro VC, et al. 2013. Omega-3 fatty acids enhance phagocytosis of Alzheimer’s disease-related amyloid-beta42 by human microglia and decrease inflammatory markers. J. Alzheimers Dis. 35: 697–713. [PubMed] [Google Scholar]
- Huang WL, King VR, Curran OE, et al. 2007. A combination of intravenous and dietary docosahexaenoic acid significantly improves outcome after spinal cord injury. Brain 130: 3004–3019. [CrossRef] [PubMed] [Google Scholar]
- Kiecolt-Glaser JK, Belury MA, Porter K, Beversdorf DQ, Lemeshow S, Glaser R. 2007. Depressive symptoms, omega-6:omega-3 fatty acids, and inflammation in older adults. Psychosom. Med. 69: 217–224. [CrossRef] [PubMed] [Google Scholar]
- Kiecolt-Glaser JK, Belury MA, Andridge R, Malarkey WB, Glaser R. 2011. Omega-3 supplementation lowers inflammation and anxiety in medical students: a randomized controlled trial. Brain Behav. Immun. 25: 1725–1734. [CrossRef] [PubMed] [Google Scholar]
- Kiecolt-Glaser JK, Epel ES, Belury MA, et al. 2013. Omega-3 fatty acids, oxidative stress, and leukocyte telomere length: A randomized controlled trial. Brain Behav. Immun. 28: 16–24. [CrossRef] [PubMed] [Google Scholar]
- Krabbe G, Halle A, Matyash V, et al. 2013. Functional impairment of microglia coincides with Beta-amyloid deposition in mice with Alzheimer-like pathology. PLoS One 8: e60921. [CrossRef] [PubMed] [Google Scholar]
- Krstic D, Madhusudan A, Doehner J, et al. 2012. Systemic immune challenges trigger and drive Alzheimer-like neuropathology in mice. J. Neuroinflammation 9: 151. [CrossRef] [PubMed] [Google Scholar]
- Labrousse VF, Nadjar A, Joffre C, Costes L, Aubert A, Gregoire S, Bretillon L, Laye S. 2012. Short-term long chain omega3 diet protects from neuroinflammatory processes and memory impairment in aged mice. PLoS One 7: e36861. [CrossRef] [PubMed] [Google Scholar]
- Lalancette-Hebert M, Gowing G, Simard A, Weng YC, Kriz J. 2007. Selective ablation of proliferating microglial cells exacerbates ischemic injury in the brain. J. Neurosci. 27: 2596–2605. [CrossRef] [PubMed] [Google Scholar]
- Lalancette-Hebert M, Julien C, Cordeau P, et al. 2011. Accumulation of dietary docosahexaenoic acid in the brain attenuates acute immune response and development of postischemic neuronal damage. Stroke 42: 2903–2909. [CrossRef] [PubMed] [Google Scholar]
- Laye S. 2010. Polyunsaturated fatty acids, neuroinflammation and well being. Prostaglandins Leukot Essent Fatty Acids 82: 295–303. [CrossRef] [PubMed] [Google Scholar]
- Laye S, Parnet P, Goujon E, Dantzer R. 1994. Peripheral administration of lipopolysaccharide induces the expression of cytokine transcripts in the brain and pituitary of mice. Brain Res. Mol. Brain Res. 27: 157–162. [CrossRef] [PubMed] [Google Scholar]
- Li L, Wu Y, Wang Y, Wu J, et al. 2014. Resolvin D1 promotes the interleukin-4-induced alternative activation in BV-2 microglial cells. J. Neuroinflammation 11: 72. [CrossRef] [PubMed] [Google Scholar]
- Lim SN, Huang W, Hall JC, Michael-Titus AT, Priestley JV. 2013. Improved outcome after spinal cord compression injury in mice treated with docosahexaenoic acid. Exp. Neurol. 239: 13–27. [CrossRef] [PubMed] [Google Scholar]
- Liu Y, Chen F, Odle J, Lin X, Jacobi SK, Zhu H, Wu Z, Hou Y. 2012. Fish oil enhances intestinal integrity and inhibits TLR4 and NOD2 signaling pathways in weaned pigs after LPS challenge. J. Nutr. 142: 2017–2024. [CrossRef] [PubMed] [Google Scholar]
- Lu Y, Zhao LX, Cao DL, Gao YJ. 2013. Spinal injection of docosahexaenoic acid attenuates carrageenan-induced inflammatory pain through inhibition of microglia-mediated neuroinflammation in the spinal cord. Neuroscience 241: 22–31. [CrossRef] [PubMed] [Google Scholar]
- Lukiw WJ, Cui JG, Marcheselli VL, et al. 2005. A role for docosahexaenoic acidderived neuroprotectin D1 in neural cell survival and Alzheimer disease. J. Clin. Invest. 115: 2774–2783. [CrossRef] [PubMed] [Google Scholar]
- Lynch AM, Moore M, Craig S, Lonergan PE, Martin DS, Lynch MA. 2003. Analysis of interleukin-1 beta-induced cell signaling activation in rat hippocampus following exposure to gamma irradiation. Protective effect of eicosapentaenoic acid. J. Biol. Chem. 278: 51075–51084. [CrossRef] [PubMed] [Google Scholar]
- Lynch AM, Loane DJ, Minogue AM, et al. 2007. Eicosapentaenoic acid confers neuroprotection in the amyloid-beta challenged aged hippocampus. Neurobiol. Aging. 28: 845–855. [CrossRef] [PubMed] [Google Scholar]
- Ma QL, Yang F, Rosario ER, et al. 2009. Beta-amyloid oligomers induce phosphorylation of tau and inactivation of insulin receptor substrate via c-Jun N-terminal kinase signaling: suppression by omega-3 fatty acids and curcumin. J. Neurosci. 29: 9078–9089. [CrossRef] [PubMed] [Google Scholar]
- Madore C, Nadjar A, Delpech JC, et al. 2014. Nutritional n-3 PUFAs deficiency during perinatal periods alters brain innate immune system and neuronal plasticity-associated genes. Brain Behav. Immun. 41: 22–31. [Google Scholar]
- Marcheselli VL, Mukherjee PK, Arita M, et al. 2010. Neuroprotectin D1/protectin D1 stereoselective and specific binding with human retinal pigment epithelial cells and neutrophils. Prostaglandins Leukot Essent Fatty. Acids. 82: 27–34. [CrossRef] [Google Scholar]
- McGeer PL, McGeer EG. 2007. NSAIDs and Alzheimer disease: epidemiological, animal model and clinical studies. Neurobiol. Aging. 28: 639–647. [CrossRef] [PubMed] [Google Scholar]
- McNamara RK, Jandacek R, Rider T, Tso P, Cole-Strauss A, Lipton JW. 2010. Omega-3 fatty acid deficiency increases constitutive pro-inflammatory cytokine production in rats: relationship with central serotonin turnover. Prostaglandins Leukot Essent Fatty Acids 83: 185–191. [CrossRef] [PubMed] [Google Scholar]
- Meydani SN, Lichtenstein AH, White PJ, et al. 1991. Food use and health effects of soybean and sunflower oils. J. Am. Coll. Nutr. 10: 406–428. [CrossRef] [PubMed] [Google Scholar]
- Michaeli B, Berger MM, Revelly JP, Tappy L, Chiolero R. 2007. Effects of fish oil on the neuro-endocrine responses to an endotoxin challenge in healthy volunteers. Clin. Nutr. 26: 70–77. [CrossRef] [PubMed] [Google Scholar]
- Mingam R, Moranis A, Bluthe RM, et al. 2008. Uncoupling of interleukin-6 from its signalling pathway by dietary n-3-polyunsaturated fatty acid deprivation alters sickness behaviour in mice. Eur. J. Neurosci. 28: 1877–1886. [CrossRef] [PubMed] [Google Scholar]
- Minogue AM, Lynch AM, Loane DJ, Herron CE, Lynch MA. 2007. Modulation of amyloid-beta-induced and age-associated changes in rat hippocampus by eicosapentaenoic acid. J. Neurochem. 103: 914–926. [CrossRef] [PubMed] [Google Scholar]
- Moranis A, Delpech JC, De Smedt-Peyrusse V, et al. 2012. Long term adequate n-3 polyunsaturated fatty acid diet protects from depressive-like behavior but not from working memory disruption and brain cytokine expression in aged mice. Brain Behav. Immun. 26: 721–731. [Google Scholar]
- Neurauter G, Schrocksnadel K, Scholl-Burgi S, et al. 2008. Chronic immune stimulation correlates with reduced phenylalanine turnover. Curr. Drug. Metab. 9: 622–627. [CrossRef] [PubMed] [Google Scholar]
- Ngandu T, Lehtisalo J, Solomon A, et al. 2015. A 2 year multidomain intervention of diet, exercise, cognitive training, and vascular risk monitoring versus control to prevent cognitive decline in at-risk elderly people (FINGER): a randomised controlled trial. Lancet 6: 2255–63. [CrossRef] [PubMed] [Google Scholar]
- Nguyen LN, Ma D, Shui G, et al. 2014. Mfsd2a is a transporter for the essential omega-3 fatty acid docosahexaenoic acid. Nature 509: 503–506. [CrossRef] [PubMed] [Google Scholar]
- Odusanwo O, Chinthamani S, McCall A, Duffey ME, Baker OJ. 2012. Resolvin D1 prevents TNF-alpha-mediated disruption of salivary epithelial formation. Am. J. Physiol. Cell. Physiol. 302: C1331–1345. [CrossRef] [PubMed] [Google Scholar]
- Olmos G, Llado J. 2014. Tumor necrosis factor alpha: a link between neuroinflammation and excitotoxicity. Mediators. Inflamm. 2014: 861231. [CrossRef] [PubMed] [Google Scholar]
- Ong WY, Farooqui T, Kokotos G, Farooqui AA. 2015. Synthetic and Natural Inhibitors of Phospholipases A: Their Importance for Understanding and Treatment of Neurological Disorders. ACS Chem. Neurosci. 6: 814–31. [CrossRef] [PubMed] [Google Scholar]
- Orr SK, Bazinet RP. 2008. The emerging role of docosahexaenoic acid in neuroinflammation. Curr. Opin. Investig. Drugs 9: 735–743. [PubMed] [Google Scholar]
- Orr SK, Palumbo S, Bosetti F, et al. 2013. Unesterified docosahexaenoic acid is protective in neuroinflammation. J. Neurochem. 127: 378–393. [CrossRef] [PubMed] [Google Scholar]
- Oxenkrug G. 2011. Interferon-gamma-Inducible Inflammation: Contribution to Aging and Aging-Associated Psychiatric Disorders. Aging. Dis. 2: 474–486. [PubMed] [Google Scholar]
- Perry VH, Nicoll JA, Holmes C. 2010. Microglia in neurodegenerative disease. Nat. Rev. Neurol. 6: 193–201. [Google Scholar]
- Pierdomenico AM, Recchiuti A, Simiele F, et al. 2015. MicroRNA-181b regulates ALX/FPR2 receptor expression and proresolution signaling in human macrophages. J. Biol. Chem. 290: 3592–3600. [CrossRef] [PubMed] [Google Scholar]
- Rapoport SI. 2008. Brain arachidonic and docosahexaenoic acid cascades are selectively altered by drugs, diet and disease. Prostaglandins Leukot Essent Fatty Acids 79: 153–156. [CrossRef] [PubMed] [Google Scholar]
- Rees D, Miles EA, Banerjee T, et al. 2006. Dose-related effects of eicosapentaenoic acid on innate immune function in healthy humans: a comparison of young and older men. Am. J. Clin. Nutr. 83: 331–342. [Google Scholar]
- Rice DS, Calandria JM, Gordon WC, et al. 2015. Adiponectin receptor 1 conserves docosahexaenoic acid and promotes photoreceptor cell survival. Nat. Commun. 4: 6:6228. [Google Scholar]
- Rockett BD, Franklin A, Harris M, Teague H, Rockett A, Shaikh SR. 2011. Membrane raft organization is more sensitive to disruption by (n-3) PUFA than nonraft organization in EL4 and B cells. J. Nutr. 141: 1041–1048. [CrossRef] [PubMed] [Google Scholar]
- Ruth MR, Proctor SD, Field CJ. 2009. Feeding long-chain n-3 polyunsaturated fatty acids to obese leptin receptor-deficient JCR:LA- cp rats modifies immune function and lipid-raft fatty acid composition. Br. J. Nutr. 101: 1341–1350. [CrossRef] [PubMed] [Google Scholar]
- Scheltens P, Twisk JW, Blesa R, et al. 2012. Efficacy of Souvenaid in mild Alzheimer’s disease: results from a randomized, controlled trial. J. Alzheimers Dis. 31: 225–36. [PubMed] [Google Scholar]
- Serhan CN. 2007. Resolution phase of inflammation: novel endogenous anti-inflammatory and proresolving lipid mediators and pathways. Annu. Rev. Immunol. 25: 101–137. [CrossRef] [PubMed] [Google Scholar]
- Serhan CN, Chiang N. 2013. Resolution phase lipid mediators of inflammation: agonists of resolution. Curr. Opin. Pharmacol. 13: 632–640. [CrossRef] [PubMed] [Google Scholar]
- Serhan CN, Brain SD, Buckley CD, et al. 2007. Resolution of inflammation: state of the art, definitions and terms. Faseb. J. 21: 325–332. [CrossRef] [PubMed] [Google Scholar]
- Serhan CN, Fredman G, Yang R, et al. 2011. Novel proresolving aspirin-triggered DHA pathway. Chem. Biol. 18: 976–987. [CrossRef] [PubMed] [Google Scholar]
- Serhan CN, Dalli J, Colas RA, Winkler JW, Chiang N. 2015. Protectins and maresins: New pro-resolving families of mediators in acute inflammation and resolution bioactive metabolome. Biochim. Biophys. Acta 1851: 397–413. [Google Scholar]
- Sijben JW, Calder PC. 2007. Differential immunomodulation with long-chain n-3 PUFA in health and chronic disease. Proc. Nutr. Soc. 66: 237–259. [CrossRef] [PubMed] [Google Scholar]
- Song BJ, Elbert A, Rahman T, Orr SK, Chen CT, Febbraio M, Bazinet RP. 2010. Genetic ablation of CD36 does not alter mouse brain polyunsaturated fatty acid concentrations. Lipids 45: 291–299. [CrossRef] [PubMed] [Google Scholar]
- Song C, Leonard BE, Horrobin DF. 2004. Dietary ethyl-eicosapentaenoic acid but not soybean oil reverses central interleukin-1-induced changes in behavior, corticosterone and immune response in rats. Stress 7: 43–54. [CrossRef] [PubMed] [Google Scholar]
- Song C, Manku MS, Horrobin DF. 2008. Long-chain polyunsaturated fatty acids modulate interleukin-1beta-induced changes in behavior, monoaminergic neurotransmitters, and brain inflammation in rats. J. Nutr. 138: 954–963. [CrossRef] [PubMed] [Google Scholar]
- Sparkman NL, Martin LA, Calvert WS, Boehm GW. 2005. Effects of intraperitoneal lipopolysaccharide on Morris maze performance in year-old and 2-month-old female C57BL/6J mice. Behav. Brain Res. 159: 145–151. [CrossRef] [PubMed] [Google Scholar]
- Sundaram JR, Poore CP, Sulaimee NH, Pareek T, Asad AB, Rajkumar R, Cheong WF, Wenk MR, Dawe GS, Chuang KH, Pant HC, Kesavapany S. 2013. Specific inhibition of p25/Cdk5 activity by the Cdk5 inhibitory peptide reduces neurodegeneration in vivo. J. Neurosci. 33: 334–343. [CrossRef] [PubMed] [Google Scholar]
- Tremblay ME, Stevens B, Sierra A, Wake H, Bessis A, Nimmerjahn A. 2011. The role of microglia in the healthy brain. J. Neurosci. 31: 16064–16069. [CrossRef] [PubMed] [Google Scholar]
- Vauzour D. 2012. Dietary polyphenols as modulators of brain functions: biological actions and molecular mechanisms underpinning their beneficial effects. Oxid. Med. Cell. Longev. 2012: 914273. [Google Scholar]
- Vedin I, Cederholm T, Freund Levi Y, et al. 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: 1616–1622. [CrossRef] [PubMed] [Google Scholar]
- Wang Q, Zheng X, Cheng Y, et al. 2014. Resolvin D1 stimulates alveolar fluid clearance through alveolar epithelial sodium channel, Na,K-ATPase via ALX/cAMP/PI3K pathway in lipopolysaccharide-induced acute lung injury. J. Immunol. 192: 3765–3777. [CrossRef] [PubMed] [Google Scholar]
- Wang X, Hjorth E, Vedin I, et al. 2015a. Effects of n-3 FA supplementation on the release of proresolving lipid mediators by blood mononuclear cells: the OmegAD study. J. Lipid. Res. 56: 674–681. [Google Scholar]
- Wang X, Zhu M, Hjorth E, et al. 2015b. Resolution of inflammation is altered in Alzheimer’s disease. Alzheimers Dement 11: 40-50 e41-42. [CrossRef] [PubMed] [Google Scholar]
- Xu MX, Tan BC, Zhou W, et al. 2013, Resolvin D1, an endogenous lipid mediator for inactivation of inflammation-related signaling pathways in microglial cells, prevents lipopolysaccharide-induced inflammatory responses. CNS Neurosci. Ther. 19: 235–243. [CrossRef] [PubMed] [Google Scholar]
- Yang L, Zhang Y, Wang S, Zhang W, Shi R. 2014. Decreased liver peroxisomal beta-oxidation accompanied by changes in brain fatty acid composition in aged rats. Neurol. Sci. 35: 289–293. [CrossRef] [PubMed] [Google Scholar]
- Yates CM, Calder PC, Ed Rainger G. 2014. Pharmacology and therapeutics of omega-3 polyunsaturated fatty acids in chronic inflammatory disease. Pharmacol. Ther. 141: 272–282. [CrossRef] [PubMed] [Google Scholar]
- Yehuda S, Rabinovitz S, Carasso RL, Mostofsky DI. 2002. The role of polyunsaturated fatty acids in restoring the aging neuronal membrane. Neurobiol. Aging. 23: 843–853. [CrossRef] [PubMed] [Google Scholar]
- Yehuda S, Rabinovitz S, Mostofsky DI. 2005. Essential fatty acids and the brain: from infancy to aging. Neurobiol. Aging 26: 98–102. [Google Scholar]
- Zamzow DR, Elias V, Legette LL, Choi J, Stevens JF, Magnusson KR. 2014. Xanthohumol improved cognitive flexibility in young mice. Behav. Brain Res. 275: 1–10. [CrossRef] [PubMed] [Google Scholar]
- Zhu M, Wang X, Schultzberg M, Hjorth E. 2015. Differential regulation of resolution in inflammation induced by amyloid-beta42 and lipopolysaccharides in human microglia. J. Alzheimers Dis. 43: 1237–1250. [PubMed] [Google Scholar]
- Zunszain PA, Anacker C, Cattaneo A, et al. 2012. Interleukin-1beta: a new regulator of the kynurenine pathway affecting human hippocampal neurogenesis. Neuropsychopharmacology 37: 939–949. [CrossRef] [PubMed] [Google Scholar]
Cite this article as: Quentin Leyrolle, Sophie Layé, Agnès Nadjar. N-3 PUFAs and neuroinflammatory processes in cognitive disorders. OCL 2016, 23(1) D103.
Current usage metrics show cumulative count of Article Views (full-text article views including HTML views, PDF and ePub downloads, according to the available data) and Abstracts Views on Vision4Press platform.
Data correspond to usage on the plateform after 2015. The current usage metrics is available 48-96 hours after online publication and is updated daily on week days.
Initial download of the metrics may take a while.