scholarly journals Upregulation of Polysialylated Neural Cell Adhesion Molecule in the Dorsal Hippocampus after Contextual Fear Conditioning Is Involved in Long-Term Memory Formation

2007 ◽  
Vol 27 (17) ◽  
pp. 4552-4561 ◽  
Author(s):  
M. A. Lopez-Fernandez ◽  
M.-F. Montaron ◽  
E. Varea ◽  
G. Rougon ◽  
C. Venero ◽  
...  
Physiology ◽  
2003 ◽  
Vol 18 (4) ◽  
pp. 147-150 ◽  
Author(s):  
Hans Welzl ◽  
Oliver Stork

Experimental evidence implies that L1 and neural cell adhesion molecule (NCAM) are involved in long-term memory formation. Changes in their expression and glycosylation appear to modify the synaptic strength underlying memory consolidation. Interference with L1 and NCAM function in a variety of learning tasks in different species severely attenuates memory consolidation, indicating their involvement in an evolutionary conserved mechanism of neural plasticity.


2019 ◽  
Vol 10 (1) ◽  
Author(s):  
Li Lv ◽  
Yunlong Liu ◽  
Jianxin Xie ◽  
Yan Wu ◽  
Jianjian Zhao ◽  
...  

AbstractMemory consolidation theory suggests that once memory formation has been completed, memory is maintained at a stable strength and is incapable of further enhancement. However, the current study reveals that even long after formation, contextual fear memory could be further enhanced. Such unexpected enhancement is possible because memory is dynamically maintained at an intermediate level that allows for bidirectional regulation. Here we find that both Rac1 activation and expression of α2-chimaerin are stimulated by single-trial contextual fear conditioning. Such sustained Rac1 activity mediates reversible forgetting, and α2-chimaerin acts as a memory molecule that reverses forgetting to sustain memory through inhibition of Rac1 activity during the maintenance stage. Therefore, the balance between activated Rac1 and expressed α2-chimaerin defines dynamic long-term memory maintenance. Our findings demonstrate that consolidated memory maintains capacity for bidirectional regulation.


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