Hippocampal levels of phosphorylated protein kinase a (phosphor-S96) are linked to spatial memory enhancement by SGS742

Hippocampus ◽  
2009 ◽  
Vol 19 (1) ◽  
pp. 90-98 ◽  
Author(s):  
Berta Sunyer ◽  
Ki-Shuk Shim ◽  
Gunyong An ◽  
Harald Höger ◽  
Gert Lubec
2004 ◽  
Vol 172 (12) ◽  
pp. 7804-7812 ◽  
Author(s):  
Michael R. Elliott ◽  
Ryan A. Shanks ◽  
Islam U. Khan ◽  
James W. Brooks ◽  
Pamela J. Burkett ◽  
...  

2012 ◽  
Vol 101 (3) ◽  
pp. 311-319 ◽  
Author(s):  
Ali Hosseini-Sharifabad ◽  
Mohammad Hossein Ghahremani ◽  
Omid Sabzevari ◽  
Naser Naghdi ◽  
Mohammad Abdollahi ◽  
...  

2006 ◽  
Vol 26 (8) ◽  
pp. 2936-2946 ◽  
Author(s):  
Barbara Kaltschmidt ◽  
Delphine Ndiaye ◽  
Martin Korte ◽  
Stéphanie Pothion ◽  
Laurence Arbibe ◽  
...  

ABSTRACT Synaptic activity-dependent de novo gene transcription is crucial for long-lasting neuronal plasticity and long-term memory. In a forebrain neuronal conditional NF-κB-deficient mouse model, we demonstrate here that the transcription factor NF-κB regulates spatial memory formation, synaptic transmission, and plasticity. Gene profiling experiments and analysis of regulatory regions identified the α catalytic subunit of protein kinase A (PKA), an essential memory regulator, as a new NF-κB target gene. Consequently, NF-κB inhibition led to a decrease in forskolin-induced CREB phosphorylation. Collectively, these results disclose a novel hierarchical transcriptional network involving NF-κB, PKA, and CREB that leads to concerted nuclear transduction of synaptic signals in neurons, accounting for the critical function of NF-κB in learning and memory.


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