Abstract

Decreased brain content of DHA, the most abundant long-chain n-3 polyunsaturated fatty acid (n-3 LCPUFA) in the brain, is accompanied by severe neurosensorial impairments linked to impaired neurotransmission and impaired brain glucose utilization. In the present study, we hypothesized that increasing n-3 LCPUFA intake at an early age may help to prevent or correct the glucose hypometabolism observed during aging and age-related cognitive decline. The effects of 12 months' supplementation with n-3 LCPUFA on brain glucose utilization assessed by positron emission tomography was tested in young adult mouse lemurs (Microcebus murinus). Cognitive function was tested in parallel in the same animals. Lemurs supplemented with n-3 LCPUFA had higher brain glucose uptake and cerebral metabolic rate of glucose compared with controls in all brain regions. The n-3 LCPUFA-supplemented animals also had higher exploratory activity in an open-field task and lower evidence of anxiety in the Barnes maze. Our results demonstrate for the first time in a nonhuman primate that n-3 LCPUFA supplementation increases brain glucose uptake and metabolism and concomitantly reduces anxiety.

Highlights

  • Decreased brain content of DHA, the most abundant long-chain n-3 polyunsaturated fatty acid (n-3 longchain polyunsaturated fatty acid (LCPUFA)) in the brain, is accompanied by severe neurosensorial impairments linked to impaired neurotransmission and impaired brain glucose utilization

  • Fish oil-supplemented animals exhibited a 3.4-fold increase in total n-3 PUFAs compared with controls while total n-6 and monounsaturated fatty acids concurrently decreased ‫ف‬40% (P < 0.01) and 30% (P < 0.01), respectively

  • The present results demonstrate for the first time that n-3 LCPUFA supplementation can lead to improved glucose entry and utilization into the primate brain

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Summary

Introduction

Decreased brain content of DHA, the most abundant long-chain n-3 polyunsaturated fatty acid (n-3 LCPUFA) in the brain, is accompanied by severe neurosensorial impairments linked to impaired neurotransmission and impaired brain glucose utilization. Long-chain n-3 PUFAs from fish oil enhance resting state brain glucose utilization and reduce anxiety in an adult nonhuman primate, the grey mouse lemur. Dietary deficiency of n-3 PUFAs leads to decreased brain content of DHA, which is accompanied by severe neurosensorial impairments (learning, memory, and anxiety) that have been linked to changes in neurotransmission processes [2]. Impairment of neurotransmission in animals fed an n-3 PUFA-deficient diet could be due in part to suboptimal brain energy metabolism.

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