Elsevier

Neurobiology of Learning and Memory

Volume 156, December 2018, Pages 103-116
Neurobiology of Learning and Memory

Chemogenetic inactivation of the dorsal hippocampus and medial prefrontal cortex, individually and concurrently, impairs object recognition and spatial memory consolidation in female mice

https://doi.org/10.1016/j.nlm.2018.11.002Get rights and content
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Highlights

  • Medial prefrontal (mPFC) inactivation impairs both spatial and object memories.

  • Effects of dorsal hippocampal inactivation (DH) on memory depend on DREADD type.

  • Episodic memory consolidation requires concurrent activation of the DH and mPFC.

Abstract

The dorsal hippocampus (DH) and medial prefrontal cortex (mPFC) are brain regions essential for processing and storing episodic memory. In rodents, the DH has a well-established role in supporting the consolidation of episodic-like memory in tasks such as object recognition and object placement. However, the role of the mPFC in the consolidation of episodic-like memory tasks remains controversial. Therefore, the present study examined involvement of the DH and mPFC, alone and in combination, in object and spatial recognition memory consolidation in ovariectomized female mice. To this end, we utilized two types of inhibitory Designer Receptors Exclusively Activated by Designer Drugs (DREADDs) to inactivate the DH alone, the mPFC alone, or both brain regions concurrently immediately after object training to assess the role of each region in the consolidation of object recognition and spatial memories. Our results using single and multiplexed DREADDS suggest that excitatory activity in the DH and mPFC, alone or in combination, is required for the successful consolidation of object recognition and spatial memories. Together, these studies provide critical insight into how the DH and mPFC work in concert to facilitate memory consolidation in female mice.

Keywords

DREADD
CNO
SALB
Hippocampus
Memory
Object placement

Cited by (0)

1

Present address: Department of Neurobiology, University of Alabama at Birmingham, Birmingham, AL 35294, United States.

2

Present address: V.A. Pittsburgh Healthcare System, Pittsburgh, PA 15216, United States.