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Reduction of dynamin 1 in the hippocampus of aged mice is associated with the decline in hippocampal-dependent memory

Authors :
Moo Ho Won
Hee Sun Yim
Hyo Young Jung
In Koo Hwang
Dae Young Yoo
Dae Won Kim
Jun-Gyo Suh
Jong Whi Kim
Yeo Sung Yoon
Hajin Nam
Jung Hoon Choi
Source :
Molecular Medicine Reports. 14:4755-4760
Publication Year :
2016
Publisher :
Spandidos Publications, 2016.

Abstract

Dynamin 1 is a known synaptic protein, which has is key in the presynaptic regulation of endocytosis. The present study investigated the association between age and the observed changes in Morris water maze performance, and immunoreactivity and protein levels of dynamin 1 in the mouse hippocampal formation. In addition, the effects of dynasore, an inhibitor of dynamin 1, on the hippocampal dependent memory were determined to elucidate the correlation between dynamin 1 and memory. In the training phase of the Morris water maze task, the mean escape latency of the aged group (24 months old) was significantly longer, compared with that of the adult group (4 months old), although the average swimming speed and the total distance traveled during the probe trial were similar in the two groups. In the aged group, the time spent locating the target platform was significantly longer and the time spent in the correct quadrant was significantly shorter, compared with those in the adult group. In the adult group, a moderate level of dynamin 1 was detected in the hippocampal CA1 and CA3 regions, and in the dentate gyrus. In the aged group, the immunoreactivity of dynamin 1 was almost eliminated in the CA3 region and the dentate gyrus. In addition, the protein levels of dynamin 1 in the brain were significantly lower in the aged group, compared with those in the adult group. The direct infusion of dynasore, significantly reduced the contextual memory, compared with that of animals in the vehicle‑treated group. These results suggested that dynamin 1 was susceptible to the aging process, and that a reduction in dynamin 1 may result in hippocampal‑dependent memory deficits by disrupting endocytosis and the release of neurotransmitters.

Details

ISSN :
17913004 and 17912997
Volume :
14
Database :
OpenAIRE
Journal :
Molecular Medicine Reports
Accession number :
edsair.doi.dedup.....b1f22507992d61bad2e5b0e26d9ffb43
Full Text :
https://doi.org/10.3892/mmr.2016.5804