4.6 Article

Changes in mGlu5 Receptor Signaling Are Associated with Associative Learning and Memory Extinction in Mice

Journal

LIFE-BASEL
Volume 12, Issue 3, Pages -

Publisher

MDPI
DOI: 10.3390/life12030463

Keywords

mGlu5 receptors; polyphosphoinositide hydrolysis; VU0360172; spatial learning; extinction; hippocampus; prefrontal cortex; G alpha q; PLC-beta; norbin

Funding

  1. Sapienza [RM120172B98E1C47]

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This study investigates the effects of spatial learning and memory extinction on mGlu5 metabotropic glutamate receptor signaling in the hippocampus and prefrontal cortex. The results show that mGlu5 receptor-mediated PI hydrolysis is reduced in the dorsal hippocampus of learner mice compared to naive and control mice. Memory extinction is associated with an up-regulation of mGlu5 receptor-mediated PI hydrolysis in the three brain regions and an increase in mGlu5 receptor and phospholipase-C beta protein levels in the ventral and dorsal hippocampus, respectively.
Using an in vivo method for the assessment of polyphosphoinositide (PI) hydrolysis, we examine whether spatial learning and memory extinction cause changes in mGlu5 metabotropic glutamate receptor signaling in the hippocampus and prefrontal cortex. We use the following five groups of mice: (i) naive mice; (ii) control mice exposed to the same environment as learner mice; (iii) leaner mice, trained for four days in a water maze; (iv) mice in which memory extinction was induced by six trials without the platform; (v) mice that spontaneously lost memory. The mGlu5 receptor-mediated PI hydrolysis was significantly reduced in the dorsal hippocampus of learner mice as compared to naive and control mice. The mGlu5 receptor signaling was also reduced in the ventral hippocampus and prefrontal cortex of learner mice, but only with respect to naive mice. Memory extinction was associated with a large up-regulation of mGlu5 receptor-mediated PI hydrolysis in the three brain regions and with increases in mGlu5 receptor and phospholipase-C beta protein levels in the ventral and dorsal hippocampus, respectively. These findings support a role for mGlu5 receptors in mechanisms underlying spatial learning and suggest that mGlu5 receptors are candidate drug targets for disorders in which cognitive functions are impaired or aversive memories are inappropriately retained.

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