# The Habenula’s role in major depressive disorder: recent insights from preclinical and human studies

**Authors:** Feiteng Lin, Kayleigh Casmey, Sierra A. Codeluppi-Arrowsmith, Gustavo Turecki

PMC · DOI: 10.1038/s41398-026-03867-0 · 2026-02-07

## TL;DR

This review explores how the habenula, a brain region, is linked to depression and how its dysfunction may contribute to mood disorders.

## Contribution

The paper highlights subregion-specific molecular and neurocircuitry changes in the habenula associated with depression.

## Key findings

- The medial habenula shows downregulated CAPS2 and nicotinic signaling in depression.
- The lateral habenula exhibits dysregulated Kir4.1, CaMKIIβ, PP2A, and SNORA69 in depression models.
- MDD is associated with structural and functional changes in the habenula, including reduced cell counts and connectivity.

## Abstract

The habenula is a small epithalamic structure composed of two distinct subregions, the medial (MHb) and lateral (LHb) habenula. It serves as a critical hub for integrating fronto-limbic and brainstem signals to regulate motivation, mood, and reward processing. Therefore, it is unsurprising that dysfunction of the habenula has been implicated in several mood disorders including major depressive disorder (MDD), a debilitating mood disorder marked by low mood and feelings of hopelessness. This review synthesizes recent advances in understanding the habenula’s neurocircuitry, molecular landscape, and role in MDD pathophysiology, while evaluating its potential as a therapeutic target. Specifically, emerging evidence highlights subregion-specific pathology. Indeed, in MDD and in animal models of depression, the MHb has been shown to exhibit marked downregulation of calcium-dependent activator protein for secretion 2 (CAPS2) and deficits in nicotinic acetylcholine receptor-mediated signaling. While in the LHb, dysregulated expression profiles of inward-rectifying potassium channel Kir4.1, the β isoform of calcium/calmodulin-dependent protein kinase II (CaMKIIβ), protein phosphatase 2 A (PP2A), and small nucleolar RNA SNORA69 have been found in animal models of depression and MDD postmortem studies. Structural imaging and postmortem neurohistological studies in MDD patients have further revealed habenular volume changes, reduced neuronal cell counts, diminished cell area, and abnormal functional connectivity. As research unravels the habenula’s complexities, its potential in treating mood disorders grows increasingly salient, offering new avenues for intervention in mental health.

## Linked entities

- **Genes:** CAPS2 (calcyphosine 2) [NCBI Gene 84698], KCNJ10 (potassium inwardly rectifying channel subfamily J member 10) [NCBI Gene 3766], CG17698 (uncharacterized protein) [NCBI Gene 4379919], PTPA (protein phosphatase 2 phosphatase activator) [NCBI Gene 5524], SNORA69 (small nucleolar RNA, H/ACA box 69) [NCBI Gene 26779]
- **Diseases:** major depressive disorder (MONDO:0002009), MDD (MONDO:0012048)

## Full-text entities

- **Genes:** CADPS2 (calcium dependent secretion activator 2) [NCBI Gene 93664] {aka CAPS2}, PTPA (protein phosphatase 2 phosphatase activator) [NCBI Gene 5524] {aka PARK25, PP2A, PPP2R4, PR53}, SNORA69 (small nucleolar RNA, H/ACA box 69) [NCBI Gene 26779] {aka RNU69, U69, U69A}, KCNJ10 (potassium inwardly rectifying channel subfamily J member 10) [NCBI Gene 3766] {aka BIRK-10, KCNJ13-PEN, KIR1.2, KIR4.1, SESAME}
- **Diseases:** depression (MESH:D003866), mood disorder (MESH:D019964), MDD (MESH:D003865)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12923909/full.md

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Source: https://tomesphere.com/paper/PMC12923909