Impacts of early life stress on the neurobiology of depression

Good Therapy NYC
PsychologyNeuroscience
$863
Raised of $12,460 Goal
7%
Ended on 4/29/21
Campaign Ended
  • $863
    pledged
  • 7%
    funded
  • Finished
    on 4/29/21

About This Project

Of the 300 million people worldwide living with depression, half do not respond to current treatments. In this population, most undergo forms of early life stress (ELS). Our group is interested in examining the impacts of ELS on the brain areas and pathways later implicated in depression. We hypothesize that ELS could cause longstanding changes in cortical and limbic cells and pathways. Understanding these impacts could lead to novel treatments both behavioral and pharmacological.

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What is the context of this research?

Our understanding of depression still has several missing pieces, and the causes are not fully understood. One subset of people living with depression undergo stressful experiences during early childhood, and show altered brain activity as adults. Additionally, depressed patients tend to have a bias in their attention and appraisal of incoming information, attending to only the negative information. While the clinical link between ELS and depression is robust, its neurobiology is gravely understudied. We intend to move this research forward, by deciphering how ELS rewires brain areas linked with depression. We will use an animal model of ELS and assess depressive behaviors and cognitive bias in adulthood, and examine their neural connectivity and function.

What is the significance of this project?

Of the 17 million affected Americans living with depression, almost half are unresponsive to current treatments. ELS is a large risk factor in this subgroup. An issue that we see in depressed patients and in animal models of depression is a decrease in the number and diversity of neural connections. This decrease has been linked with adult stress in animal models. We will test the hypothesis that ELS reduces neural connectivity, neuronal function, and elicits depressive behavior. Testing this hypothesis will define the role of ELS in the etiology of depression. Significantly, it will mobilize a research program aimed towards behavioral and drug treatments that restore neuronal connections.

What are the goals of the project?

These experiments will demonstrate the impact of ELS on two brain areas implicated in depression, as well as on behavioral outcomes in depressive symptoms and cognitive-affective bias. Our studies examine ELS impacts compared to controls as well as adult stress groups, currently used as an animal model of depression. Electrophysiology experiments will determine differences in cell physiology, in presynaptic and postsynaptic function. IHC will illustrate disparities in relation to cell morphology and dendrite architecture. Behavioral assessments will compare the different stress groups in depressive phenotyopes and cognitive bias. The outcome would be a novel understanding of the neurobiology of depression that could to give new potential targets for treatment.

Budget

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We are requesting funding to cover laboratory supplies, core facility fees and animals costs to carry out the proposed research project. Research supplies are calculated at approximately $10,060 throughout the project period, and include reagents for electrophysiology and immunohistochemistry studies as well as confocal microscopy user fees. Animal Costs (mice colony) costs are calculated at approximately $2,400 throughout the project period, and include housing, keeping, tagging and genotyping.

Endorsed by

I think this is an incredibly important study and area of research! It may provide important insight as well as clinical implications on the connection between early life stress and depression later in life. Also, Ernie is a fantastic clinician and researcher!
Mr. Cote’s clinical work, teaching record, and research has always been mirrored by innovative ideas and exceeding expectations. His current research on early stress on the neural impact of depression is groundbreaking. This project will enhance knowledge of depression at a neurobiological level while providing better insight to inform the development of more targeted, evidence-based pharmacological and psychological therapeutic interventions to improve depression treatment outcomes. Mr. Cote’s methodology is rigorous, analytical, and sound.
The area of early life stress on the neurobiology of depression is such an important area of study. This topic has not been extensively researched. The findings of this study may be impactful in ways of approaching psychological therapy, as well as psychopharmacology and beyond. Mr. Ernie Cote is a great researcher, educator and clinician and I have no doubt that his research results will add to the broader impact of the literature in the field.

Project Timeline

We began collecting data in early January 2021. We are using a minimal number of animals, and will get multiple data points from each animal. The first set of experiments will complete the behavioral tests as well as the electrophysiology. These data points are connected, and finish about the same timeline. Once that is complete, we will concentrate on morphology/IHC, and finally we will assess cortisol differences and sex differences from blood and swabs taken at sacrifice.

Mar 15, 2021

Project Launched

May 15, 2021

Complete Behavioral assessments for each group. Illustrate any differences (or similarities) between controls and stress groups.

May 31, 2021

Complete electrophysiology and data analysis on Input/output and frequency tuning.

Jul 31, 2021

Complete IHC and data analysis on dendrite architecture and cell counts in areas of interest.

Meet the Team

Ernie Cote
Ernie Cote
Ph.D, LMHC-D

Ernie Cote

My research is historically at the intersection of neuroscience, mental health, and more recently- human performance. My earlier work focused on the neurobiology of trauma and early life stress using both animal models and human research approaches. These projects explored how stress during development can alter brain circuits involved in emotion, motivation, and reward. Understanding these mechanisms is critical because many psychiatric conditions, including depression and anxiety disorders, are strongly linked to adverse childhood experiences.
Concurrent with my research career, I have been a licensed psychotherapist, practicing in NYC. These clinical observations motivate my research into the biological and cognitive mechanisms underlying mental health disorders, with the goal of developing new approaches to treatment.
More recently, my work has expanded into the neuroscience of mental performance and optimal functioning in athletes, sparked by my personal hobbies in martial arts. Competitive fighters and other high-performance athletes operate in environments that place extreme demands on attention, emotional regulation, and decision making under pressure. Despite the importance of these cognitive and emotional skills, the neuroscience of peak performance in combat sports and other high-intensity athletics remains largely unexplored, and I believe that any insights we gain from researching these topics could be translated to the clinical populations in mental health.
My current research focuses on understanding the brain states that support “flow,” attention, and emotional regulation during performance. Using electroencephalography (EEG) and neurofeedback methods, I study how patterns of brain activity relate to performance under pressure. The goal of this work is to identify neural markers of optimal mental performance and develop training approaches that help athletes regulate their cognitive and emotional states more effectively.


Project Backers

  • 16Backers
  • 7%Funded
  • $863Total Donations
  • $53.94Average Donation
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