Recombinant growth differentiation factor 11 influences short-term memory and enhances Sox2 expression in middle-aged mice
•Single dose of rGDF-11 improved visual short-term memory in middle-aged mice.•No changes in spatial short-term memory were observed in middle-aged mice.•rGDF-11 treatment did not affect short-term memory in young mice.•Young mice treated with rGDF-11 had increased levels of phospho-Smad2/3 in brain...
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Published in | Behavioural brain research Vol. 341; pp. 45 - 49 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
Netherlands
Elsevier B.V
02.04.2018
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Subjects | |
Online Access | Get full text |
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Summary: | •Single dose of rGDF-11 improved visual short-term memory in middle-aged mice.•No changes in spatial short-term memory were observed in middle-aged mice.•rGDF-11 treatment did not affect short-term memory in young mice.•Young mice treated with rGDF-11 had increased levels of phospho-Smad2/3 in brain.
Previous evidence suggests that a significant decline in cognitive ability begins during middle-age and continues to deteriorate with increase in age. Recent work has demonstrated the potential rejuvenation impact of growth differentiation factor-11 (GDF-11) in aged mice. We carried out experiments to evaluate the impact of a single dose of recombinant (rGDF-11) on short-term visual and spatial memory in middle-aged male mice. On the novel object recognition task, we observed middle-aged mice treated rGDF-11 showed improved performance on the novel object recognition task. However, middle-aged mice did not show increased expression of phosphorylated-Smad2/3, a downstream effector of GDF-11. We noted however that the expression of the transcription factor, Sox2 was increased within the dentate gyrus. Our data suggest that a single injection of rGDF-11 contributes to improvements in cognitive function of middle-aged animals, which may be critical in the preservation of short-term memory capacity in old age. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0166-4328 1872-7549 |
DOI: | 10.1016/j.bbr.2017.12.019 |