2003
DOI: 10.1016/s0197-4580(02)00064-7
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DHA-enriched phospholipid diets modulate age-related alterations in rat hippocampus

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Cited by 92 publications
(67 citation statements)
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“…Animals were maintained on a balanced diet containing ALA and LA from birth to 18 months, during which time spontaneous ACh release steadily declined in the hippocampus. While the egg phospholipid diet restored both the DHA and AA content of neuronal membranes and ACh release in the hippocampus, the pig brain diet had no effect on membrane composition, but was able to restore ACh release, albeit to a lesser extent than the egg phospholipid diet [22]. In a similar study, rats were fed with diets supplemented with increasing levels of DHA derived from either egg phospholipids or tuna oil.…”
Section: Pufas and The Aging Brainmentioning
confidence: 97%
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“…Animals were maintained on a balanced diet containing ALA and LA from birth to 18 months, during which time spontaneous ACh release steadily declined in the hippocampus. While the egg phospholipid diet restored both the DHA and AA content of neuronal membranes and ACh release in the hippocampus, the pig brain diet had no effect on membrane composition, but was able to restore ACh release, albeit to a lesser extent than the egg phospholipid diet [22]. In a similar study, rats were fed with diets supplemented with increasing levels of DHA derived from either egg phospholipids or tuna oil.…”
Section: Pufas and The Aging Brainmentioning
confidence: 97%
“…The beneficial effects of PUFAs on neuronal function have traditionally been assumed to be mediated via fatty acid enrichment of neuronal membranes and alterations in membrane biophysical properties [19]. However, one study demonstrated an increase in ACh release despite no changes in membrane PUFA content [22] indicating that the effects of fatty acids on cholinergic transmission may, therefore, not be mediated exclusively by alterations in membrane composition. In addition to affecting ACh release, PUFAs have also been shown to impact ACh receptors, both nicotinic and muscarinic.…”
Section: Pufas and The Aging Brainmentioning
confidence: 99%
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“…Commentary of adiponectin (because hypertensives have peripheral insulin resistance and are more prone to develop type 2 diabetes mellitus and metabolic syndrome 32 ); (g) depressed anti-oxidant capacity; (h) enhanced sympathetic tone (catecholamines have pro-inflammatory actions 33 ) and (i) low acetylcholine levels in the brain and leukocytes (because acetylcholine is an anti-inflammatory molecule, it enhances NO generation and its levels are enhanced by AA/EPA/DHA supplementation 34,35 ). Some of the suggested studies could be performed in human beings using peripheral leukocytes and macrophages because they contain the complete intracellular machinery for the generation, release and metabolism of dietary essential fatty acids, lipoxins, resolvins, protectins, maresins, nitrolipids, catecholamines, acetylcholine and serotonin, as well as the renin-angiotensin system and anti-oxidants.…”
Section: Linoleic Acid α-Linolenic Acidmentioning
confidence: 99%
“…During aging, the level and replacement of brain PUFAs decreases, particularly in the hippocampus, cortex, striatum and hypothalamus (figure 3). Brain levels of DHA and AA diminish in aging rats who display alterations in cognition and in LTP in the hippocampus (Favreliere et al, 2003). In transgenic SAMP8 mice, in which aging is accelerated, DHA decreases with age whereas lipid peroxidation increases (Petursdottir et al, 2002).…”
Section: Consequences Of the Decrease In N-3 Pufas On Age-related Neumentioning
confidence: 99%