Depression is a common disease that causes significant morbidity and mortality in humans. There is currently a poor understanding regarding the underlying molecular, cellular or circuit mechanisms. Presently, therapeutic intervention is not well understood mechanistically and often unsuccessful. It is important to derive a mechanistic understand of depressive disorders so that effective treatment can be developed. In this project, based on considerable preliminary data, I propose a specific hypothesis regarding modification at a synapse in the brain reward circuit that may contribute to behavioral depression. Recent studies show that neurons in the lateral habenula (LHb), a nucleus that mediates communication between forebrain and midbrain structures, increase their activity when an animal fails to receive an expected positive reward, i.e. these neurons provide a 'disappointment'signal. LHb neurons project to and modulate dopamine-rich regions such as the ventral-tegmental area (VTA), which control reward-seeking behavior and participate in depressive disorders. Our preliminary results show that excitatory synapses onto VTA-projecting LHb neurons are about significantly stronger in rat models of depression compared to control animals. Furthermore, suppression of transmission onto LHb neurons relieves depressive-like behaviors in rodent models of depression. Thus, our central hypothesis is that aberrantly potentiated excitatory synapses onto LHb neurons contribute to depression. These neurons in the LHb thus provide an abnormally strong 'disappointment'signal, which leads to reduced reward-seeking behavior, a core feature of major depression. I will combine molecular, cellular, genetic and behavioral techniques to test this hypothesis in rodent models of depression.
Neurons in the lateral habenula provide 'disappointment'signals in the brain. We have found overactive excitation by synapses onto these neurons in rodent models of depression. Thus, reducing activity of these synapses may alleviate some forms of major depressive disorders.
|Park, Hoyong; Rhee, Jeehae; Park, Kwanghoon et al. (2017) Exposure to Stressors Facilitates Long-Term Synaptic Potentiation in the Lateral Habenula. J Neurosci 37:6021-6030|
|Malinow, Roberto (2016) Depression: Ketamine steps out of the darkness. Nature 533:477-8|
|Landgraf, Dominic; Long, Jaimie E; Proulx, Christophe D et al. (2016) Genetic Disruption of Circadian Rhythms in the Suprachiasmatic Nucleus Causes Helplessness, Behavioral Despair, and Anxiety-like Behavior in Mice. Biol Psychiatry 80:827-835|
|Shabel, Steven J; Murphy, Ryan T; Malinow, Roberto (2014) Negative learning bias is associated with risk aversion in a genetic animal model of depression. Front Hum Neurosci 8:1|
|Shabel, Steven J; Proulx, Christophe D; Piriz, Joaquin et al. (2014) Mood regulation. GABA/glutamate co-release controls habenula output and is modified by antidepressant treatment. Science 345:1494-8|
|Alfonso, Stephanie; Kessels, Helmut W; Banos, Charles C et al. (2014) Synapto-depressive effects of amyloid beta require PICK1. Eur J Neurosci 39:1225-33|
|Proulx, Christophe D; Hikosaka, Okihide; Malinow, Roberto (2014) Reward processing by the lateral habenula in normal and depressive behaviors. Nat Neurosci 17:1146-52|
|Nabavi, Sadegh; Fox, Rocky; Proulx, Christophe D et al. (2014) Engineering a memory with LTD and LTP. Nature 511:348-52|
|Viger, Mathieu L; Sheng, Wangzhong; Doré, Kim et al. (2014) Near-infrared-induced heating of confined water in polymeric particles for efficient payload release. ACS Nano 8:4815-26|
|Lin, John Y; Sann, Sharon B; Zhou, Keming et al. (2013) Optogenetic inhibition of synaptic release with chromophore-assisted light inactivation (CALI). Neuron 79:241-53|
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