# Glutamatergic lateral habenula neurons modulate consolidation of associative memories

## TL;DR

This study shows that activating glutamatergic neurons in the lateral habenula disrupts long-term associative memory consolidation in mice, but ketamine can reverse this effect.

## Contribution

The study identifies a novel role for lateral habenula glutamatergic neurons in modulating memory consolidation through NMDA receptor mechanisms.

## Key findings

- Transient activation of glutamatergic lateral habenula neurons impairs long-term associative memory consolidation.
- Ketamine administration rescues memory deficits caused by lateral habenula activation.
- Memory impairment is specific to object recognition and reward-based memory, not fear-based memory.

## Abstract

Despite the rise in psychiatric disorders worldwide, the underlying brain circuits responsible for these devastating conditions remain elusive. The lateral habenula (LHb) has emerged as a key brain structure in depression studies due to its hyperactive state in both patients and animal models. While this aligns with known roles in driving aversive states and regulating serotonin release, it is still unclear how acute and transient activity changes in the LHb can influence higher order cognitive processes such as learning, memory, and behavioral adaptation. Given the importance of these processes to psychiatric conditions, understanding how LHb activity impacts cognitive function allows novel insights into the neurobiological mechanisms of disorders like depression.

Towards this goal, we used chemogenetic activation to temporarily excite glutamatergic neurons in the mouse LHb and assessed impacts on associative memory.

Surprisingly, we found that transient activation of LHb impaired long-term memory, without affecting anxiety or depression-like behaviors. Specifically, post-training activation of LHb glutamatergic neurons disrupted object recognition and reward-based associative long-term memory, while sparing fear associated long-term memory. The memory impairment was restricted to a critical temporal window post-training/conditioning that corresponded with the consolidation stage of long-term memory. Strikingly, pairing LHb glutamatergic neuronal activation with systemic ketamine administration rescued the long-term memory deficits, indicating that LHb glutamatergic neurons modulate consolidation of associative memories via a NMDA-mediated mechanism. Together, these findings support a novel role for LHb glutamatergic neuronal activity in the consolidation of associative long-term memories.