2010
DOI: 10.1016/j.jnutbio.2009.12.005
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Involvement of omega-3 fatty acids in emotional responses and hyperactive symptoms☆

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Cited by 18 publications
(9 citation statements)
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“…Although the exact mechanism by which PUFAs/EFAs decrease insulin resistance is not known, some of the possibilities include: (a) increase in the number of insulin receptors due to increased membrane fluidity; (b) an increase in GLUT-4 mRNA and protein level in adipocytes [15]; (c) formation of anti-inflammatory and anti-atherosclerotic molecules such as PGI 2 , PGE 1 , lipoxins, resolvins, protectins and maresins [16-21]; (d) suppression of the expression of adhesion molecules [22-24]; (e) inhibition of the formation of pro-inflammatory cytokines tumor necrosis factor-α (TNF-α), macrophage migration factor (MIF), high-mobility group box 1 (HMGB1) and interleukin-6 (IL-6) [25-27]; (f) enhancement in the formation of brain-derived neurotrophic factor (BDNF) in the brain and gut that has anti-diabetic actions [28-30]; and that (BDNF), in turn, augments PGI 2 synthesis [31], a potent platelet anti-aggregator, vasodilator and anti-atherosclerotic molecule; (f) enhancement in the synthesis and action of BMPs (bone morphogenetic proteins) that enhance the growth and development of the brain [32,33]; (g) modulation of the growth and actions of gut bacteria [34-37]; (h) binding to various nuclear receptors and correction of dyslipidemia [38-42]; and (i) regulation of both the secretion and actions of various hypothalamic neurotransmitters and peptides that regulate appetite, satiety, food intake and insulin secretion [43-49]. Furthermore, insulin enhances the activity of Δ 6 and Δ 5 desaturases [50] and thus, potentially augments the formation of PUFAs that, in turn, enhance the action of insulin.…”
Section: Mechanisms Of Anti-atherosclerotic Actions Of Pufasmentioning
confidence: 99%
“…Although the exact mechanism by which PUFAs/EFAs decrease insulin resistance is not known, some of the possibilities include: (a) increase in the number of insulin receptors due to increased membrane fluidity; (b) an increase in GLUT-4 mRNA and protein level in adipocytes [15]; (c) formation of anti-inflammatory and anti-atherosclerotic molecules such as PGI 2 , PGE 1 , lipoxins, resolvins, protectins and maresins [16-21]; (d) suppression of the expression of adhesion molecules [22-24]; (e) inhibition of the formation of pro-inflammatory cytokines tumor necrosis factor-α (TNF-α), macrophage migration factor (MIF), high-mobility group box 1 (HMGB1) and interleukin-6 (IL-6) [25-27]; (f) enhancement in the formation of brain-derived neurotrophic factor (BDNF) in the brain and gut that has anti-diabetic actions [28-30]; and that (BDNF), in turn, augments PGI 2 synthesis [31], a potent platelet anti-aggregator, vasodilator and anti-atherosclerotic molecule; (f) enhancement in the synthesis and action of BMPs (bone morphogenetic proteins) that enhance the growth and development of the brain [32,33]; (g) modulation of the growth and actions of gut bacteria [34-37]; (h) binding to various nuclear receptors and correction of dyslipidemia [38-42]; and (i) regulation of both the secretion and actions of various hypothalamic neurotransmitters and peptides that regulate appetite, satiety, food intake and insulin secretion [43-49]. Furthermore, insulin enhances the activity of Δ 6 and Δ 5 desaturases [50] and thus, potentially augments the formation of PUFAs that, in turn, enhance the action of insulin.…”
Section: Mechanisms Of Anti-atherosclerotic Actions Of Pufasmentioning
confidence: 99%
“…An alternative therapy for the generic treatment of depression (12), anxiety (13), and hyperactive symptoms (14) are long chain omega-3 polyunsaturated fatty acids ( n -3-LC-PUFA) and in particular eicosapentaenoic acid (EPA; 20:5 n -3) and docosahexaenoic acid (DHA; 22:6 n -3) (14). Many studies, however, regarding the effectiveness of n -3-LC-PUFA in the treatment of emotional and behavioral disorders have found inconsistent results, and the number of studies is limited, indicating a need for additional research (15).…”
Section: Introductionmentioning
confidence: 99%
“…Tsukada et al [14] demonstrated that supplementing aged monkeys with DHA for 1 to 4 weeks (a very short term dietary supplementation) led to increased regional cerebral blood flow, a parameter closely linked to neuronal activation. Since ω3 PUFA supplementation may be effective in the treatment of depressive disorder (reviewed in [15] ) it was recently proposed that they may also possess anxiolytic properties [16] . In humans, few data are available from intervention studies about the association between anxiety and ω3 fatty acids supplementation and data are divergent about the ability of dietary ω3 fatty acids to prevent age-associated cognitive decline (see [17] for review).…”
Section: Introductionmentioning
confidence: 99%