Long-term d-allose administration ameliorates age-related cognitive impairment and loss of bone strength in male mice

Age-related physical and cognitive decline may be ameliorated by consuming functional foods. d-Allose, reported to have multiple health benefits, may temper aging phenotypes, particularly brain function. We investigated whether d-allose supplementation improves cognitive function. A standard battery of behavioral tests was administered to 18-month-old male mice after consuming diet containing 3 % d-allose for 6 months. Following a wire-hanging test, an open-field test, Morris water maze, fear-conditioning, and an analgesia test were sequentially performed. Bone density and strength were assessed afterwards. Possible mechanism(s) under-lying memory changes in hippocampus were also examined with a DNA microarray. d-Allose failed to influence muscle strength, locomotor activity and anxiety, fear memory, or pain sensitivity. However, d-allose improved hippocampus-dependent spatial learning and memory, and it may contribute to increase bone strength. d-Allose also changed the expression of some genes in hippocampus involved in cognitive functions. Long-term d-allose supplementation appears to modestly change aging phenotypes and improve spatial memory.

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Publication Details

Journal
Experimental Gerontology
Published
2024-08-30
DOI
https://doi.org/10.1016/j.exger.2024.112555
Citations
4
Primary Topic
Diet and metabolism studies
Type
article
Field-Weighted Citation Impact
1.31

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Long-term d-allose administration ameliorates age-related cognitive impairment and loss of bone strength in male mice

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Diet and metabolism studies
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article

Long-term d-allose administration ameliorates age-related cognitive impairment and loss of bone strength in male mice

Shogo Endo, Shuichi Yanai, Akane Kanasaki, Tetsuo Iida, Tomoya Shintani
article en
4 citations

Abstract

Age-related physical and cognitive decline may be ameliorated by consuming functional foods. d-Allose, reported to have multiple health benefits, may temper aging phenotypes, particularly brain function. We investigated whether d-allose supplementation improves cognitive function. A standard battery of behavioral tests was administered to 18-month-old male mice after consuming diet containing 3 % d-allose for 6 months. Following a wire-hanging test, an open-field test, Morris water maze, fear-conditioning, and an analgesia test were sequentially performed. Bone density and strength were assessed afterwards. Possible mechanism(s) under-lying memory changes in hippocampus were also examined with a DNA microarray. d-Allose failed to influence muscle strength, locomotor activity and anxiety, fear memory, or pain sensitivity. However, d-allose improved hippocampus-dependent spatial learning and memory, and it may contribute to increase bone strength. d-Allose also changed the expression of some genes in hippocampus involved in cognitive functions. Long-term d-allose supplementation appears to modestly change aging phenotypes and improve spatial memory.

Experimental GerontologyVol. 196
Matsutani (Japan) (JP), Tokyo Metropolitan Institute of Gerontology (JP)
Japan Society for the Promotion of Science London
Openalex Percentile: Top 19%
Diet and metabolism studies
1.31
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