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Toru Moriguchi

Researcher at Azabu University

Publications -  52
Citations -  3296

Toru Moriguchi is an academic researcher from Azabu University. The author has contributed to research in topics: Docosahexaenoic acid & Fatty acid. The author has an hindex of 25, co-authored 50 publications receiving 3141 citations. Previous affiliations of Toru Moriguchi include National Institutes of Health.

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Journal ArticleDOI

Behavioral Deficits Associated with Dietary Induction of Decreased Brain Docosahexaenoic Acid Concentration

TL;DR: The results suggest that learning and cognitive behavior are related to brain DHA status, which, in turn, is related to the levels of themilk/dietary n‐3 fatty acids.
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Mice lacking the M3 muscarinic acetylcholine receptor are hypophagic and lean

TL;DR: It is shown that mice deficient in the M3 muscarinic receptor (M3R-/- mice) display a significant decrease in food intake, reduced body weight and peripheral fat deposits, and very low levels of serum leptin and insulin, and there may be a cholinergic pathway that involves M3-receptor-mediated facilitation of food intake at a site downstream of the hypothalamic leptin/melanocortin system and upstream of the MCH system.
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Recovery of brain docosahexaenoate leads to recovery of spatial task performance

TL;DR: The results indicate that animals repleted since birth or at weaning were able to achieve nearly the same level of brain DHA and spatial task performance as animals maintained for three generations on an n‐3 adequate diet.
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Rats with low levels of brain docosahexaenoic acid show impaired performance in olfactory-based and spatial learning tasks.

TL;DR: It is indicated that rats with decreased DHA levels in the central nervous system perform poorer in these tasks compared to rats with higher DHA Levels and suggest the presence of learning deficits in these animals.
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Reversal of docosahexaenoic acid deficiency in the rat brain, retina, liver, and serum.

TL;DR: A consideration of the total amounts and time courses of DHA repleted in the nervous system compared with the liver and circulation suggests that transport-related processes may limit the rate of D HA repletion in the retina and brain.