Ventral striatal islands of Calleja neurons bidirectionally mediate depression-like behaviors in mice

Author:

Zhang Yun-Feng1,Wang Yingqi2,Johnson Natalie3,Bhattarai Janardhan4,Espitia Camilo Guevara2,Shoenhard Hannah2ORCID,Fuccillo Marc2ORCID,Wesson Daniel3ORCID,Ma Minghong2ORCID

Affiliation:

1. Chinese Academy of Sciences

2. University of Pennsylvania School of Medicine

3. University of Florida

4. University of Pennsylvania

Abstract

Abstract The ventral striatum, composed of the nucleus accumbens (NAc) and olfactory tubercle (OT), is a key reward center implicated in the pathophysiology of depression. Although the OT is known to regulate motivational and reward-related behaviors, its involvement in depression remains unexplored. We recently report that islands of Calleja, clusters of dopamine D3 receptor-expressing granule cells that are predominately situated in the OT, regulate self-grooming, a repetitive behavior manifested in mood disorders including depression. Here we show that chronic restraint stress (CRS) induces robust depression-like behaviors in mice and decreases excitability of OT D3 neurons. Ablation or inhibition of these neurons leads to depression-like behaviors, whereas their activation ameliorates CRS-induced depressive phenotypes. Moreover, activation of OT D3 neurons has a rewarding effect, which diminishes when grooming is blocked. Finally, we propose a model to explain how OT D3 neurons may influence dopamine release into the NAc via synaptic connections with OT spiny projection neurons (SPNs) that project to midbrain dopamine neurons. Our study reveals a novel role of OT D3 neurons in bidirectionally mediating depressive phenotypes, suggesting an attractive therapeutic target.

Publisher

Research Square Platform LLC

Reference75 articles.

1. Fox, M.E. and M.K. Lobo, The molecular and cellular mechanisms of depression: a focus on reward circuitry. Mol Psychiatry, 2019. 24(12): p. 1798–1815.

2. Francis, T.C. and M.K. Lobo, Emerging role for nucleus accumbens medium spiny neuron subtypes in depression. Biological psychiatry, 2017. 81(8): p. 645–653.

3. Heshmati, M. and S.J. Russo, Anhedonia and the brain reward circuitry in depression. Current behavioral neuroscience reports, 2015. 2(3): p. 146–153.

4. Deep brain stimulation of the ventral capsule/ventral striatum for treatment-resistant depression,2009

5. Hou, Z., et al., Increased temporal variability of striatum region facilitating the early antidepressant response in patients with major depressive disorder. Progress in Neuro-Psychopharmacology and Biological Psychiatry, 2018. 85: p. 39–45.

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