Summary: Researchers have discovered a link between specific neural circuits to distinct behavioral symptoms of depression. The study, published in Cell, reports altering the networks helped to improve symptoms such as social withdrawal and helplessness.
Altering distinct brain pathways found to aid symptoms such as social withdrawal and helplessness behavior.
University of California San Diego scientists have linked specific wiring in the brain to distinct behavioral symptoms of depression.
In a study published in the journal Cell, researchers in UC San Diego’s Division of Biological Sciences found brain circuits tied to feelings of despair and helplessness and were able to alleviate and even reverse such symptoms in mice studies.
“We took an approach of studying depression in the sense that different brain areas and circuits of the brain might mediate or contribute to very discrete aspects of depression,” said study first-author Daniel Knowland, a UC San Diego graduate student. “For example, brain area A might contribute to loss of appetite, brain area B to social withdrawal and so forth.”
Senior author Byungkook Lim, an assistant professor in the Neurobiology Section, said the results require much more study and evaluation to be applied to humans with depression, but the new research in animal models provides solid grounding.
“This is one of the first studies providing clear evidence showing that different brain circuitry is involved in different types of depressive behavior with specific symptoms,” said Lim. “Each area of the brain is different with distinct cell types and connectivity, so if we can confirm that one area of circuitry is more involved in a particular symptom than another, we may eventually be able to treat a depression patient more efficiently than treating everyone the same way.”
The researchers employed several tools to track brain pathways and specific areas of neurons involved in specific behaviors, including imaging techniques and social strategy behavioral models. Two populations of neurons were identified in the brain’s ventral pallidum region (part of the basal ganglia) as key to underlying depressive behavior.
The new study found that specifically modifying pathways in these two areas in a mouse displaying depression led to improved behavioral changes similar to those of a healthy mouse. More importantly, this study provides strong insight to understanding the interaction between several brain areas in depression. Previous studies have mainly focused on the role of certain brain areas in isolation. Researchers in the new study were able to examine connections across multiple regions and how one impacted the other.
In addition to Knowland and Lim, coauthors include UC San Diego’s Varoth Lilascharoen, Christopher Pham Pacia, Sora Shin and Eric Hou-Jen Wang.
Funding: The research was supported by the Klingenstein Foundation, Searle scholar program (Kinship foundation; Searle 15-SSP-229), the Whitehall foundation (2014-08-63), NARSAD young investigator grant (24094) and grants from the National Institutes of Health (MH107742 and MH108594). Lim received a National Institute of Mental Health Biobehavioral Research Award for Innovative New Scientists (BRAINS) in 2015. Lilascharoen is supported by an Anandamahidol Foundation Fellowship.
Source: Mario Aguilera – UCSD
Image Source: NeuroscienceNews.com image is in the public domain.
Original Research: Abstract for “Distinct Ventral Pallidal Neural Populations Mediate Separate Symptoms of Depression” by Daniel Knowland, Varoth Lilascharoen, Christopher Pham Pacia, Sora Shin, Eric Hou-Jen Wang, and Byung Kook Lim in Cell. Published online July 6 2017 doi:10.1016/j.cell.2017.06.015
Distinct Ventral Pallidal Neural Populations Mediate Separate Symptoms of Depression
•VP PV neurons project to the LHb and VTA and release different transmitters
•Elevated VP PV neuronal activity is a hallmark of depressed animals
•VP PV neurons mediate distinct depressive-like symptoms based on projection target
Major depressive disorder (MDD) patients display a common but often variable set of symptoms making successful, sustained treatment difficult to achieve. Separate depressive symptoms may be encoded by differential changes in distinct circuits in the brain, yet how discrete circuits underlie behavioral subsets of depression and how they adapt in response to stress has not been addressed. We identify two discrete circuits of parvalbumin-positive (PV) neurons in the ventral pallidum (VP) projecting to either the lateral habenula or ventral tegmental area contributing to depression. We find that these populations undergo different electrophysiological adaptations in response to social defeat stress, which are normalized by antidepressant treatment. Furthermore, manipulation of each population mediates either social withdrawal or behavioral despair, but not both. We propose that distinct components of the VP PV circuit can subserve related, yet separate depressive-like phenotypes in mice, which could ultimately provide a platform for symptom-specific treatments of depression.
“Distinct Ventral Pallidal Neural Populations Mediate Separate Symptoms of Depression” by Daniel Knowland, Varoth Lilascharoen, Christopher Pham Pacia, Sora Shin, Eric Hou-Jen Wang, and Byung Kook Lim in Cell. Published online July 6 2017 doi:10.1016/j.cell.2017.06.015