Loading…

A Novel Conditional Genetic System Reveals That Increasing Neuronal cAMP Enhances Memory and Retrieval

Consistent evidence from pharmacological and genetic studies shows that cAMP is a critical modulator of synaptic plasticity and memory formation. However, the potential of the cAMP signaling pathway as a target for memory enhancement remains unclear because of contradictory findings from pharmacolog...

Full description

Saved in:
Bibliographic Details
Published in:The Journal of neuroscience 2008-06, Vol.28 (24), p.6220-6230
Main Authors: Isiegas, Carolina, McDonough, Conor, Huang, Ted, Havekes, Robbert, Fabian, Sara, Wu, Long-Jun, Xu, Hui, Zhao, Ming-Gao, Kim, Jae-Ick, Lee, Yong-Seok, Lee, Hye-Ryeon, Ko, Hyoung-Gon, Lee, Nuribalhae, Choi, Sun-Lim, Lee, Jeong-Sik, Son, Hyeon, Zhuo, Min, Kaang, Bong-Kiun, Abel, Ted
Format: Article
Language:English
Subjects:
Citations: Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:Consistent evidence from pharmacological and genetic studies shows that cAMP is a critical modulator of synaptic plasticity and memory formation. However, the potential of the cAMP signaling pathway as a target for memory enhancement remains unclear because of contradictory findings from pharmacological and genetic approaches. To address these issues, we have developed a novel conditional genetic system in mice based on the heterologous expression of an Aplysia octopamine receptor, a G-protein-coupled receptor whose activation by its natural ligand octopamine leads to rapid and transient increases in cAMP. We find that activation of this receptor transgenically expressed in mouse forebrain neurons induces a rapid elevation of hippocampal cAMP levels, facilitates hippocampus synaptic plasticity, and enhances the consolidation and retrieval of fear memory. Our findings clearly demonstrate that acute increases in cAMP levels selectively in neurons facilitate synaptic plasticity and memory, and illustrate the potential of this heterologous system to study cAMP-mediated processes in mammalian systems.
ISSN:0270-6474
1529-2401
DOI:10.1523/JNEUROSCI.2935-07.2008