Annual Review of Clinical Psychology· 2014Q1· Review
Depression, Stress, and Anhedonia: Toward a Synthesis and Integrated Model
- 1,158citations
- Q1SCImago
- 2014year
Short summary
A new model proposes that anhedonia, a key symptom of depression, stems from impaired interactions between stress and brain reward systems, specifically mesocorticolimbic dopaminergic pathways.
AI-generated from the title and abstract; the full text is not read.
Key points
- Anhedonia is proposed as a key endophenotype for depression.
- The model links anhedonia to dysfunctional interactions between stress and brain reward systems.
- Stress negatively affects mesocorticolimbic dopaminergic pathways implicated in motivation and learning.
- The paper synthesizes literature on anhedonia, dopamine, and stress to support the integrated model.
AI-generated from the title and abstract; the full text is not read.
Abstract
Depression is a significant public health problem, but its etiology and pathophysiology remain poorly understood. Such incomplete understanding likely arises from the fact that depression encompasses a heterogeneous set of disorders. To overcome these limitations, renewed interest in intermediate phenotypes (endophenotypes) has resurfaced, and anhedonia has emerged as one of the most promising endophenotypes of depression. Here, a heuristic model is presented postulating that anhedonia arises from dysfunctional interactions between stress and brain reward systems. To this end, we review and integrate three bodies of independent literature investigating the role of (a) anhedonia, (b) dopamine, and (c) stress in depression. In a fourth section, we summarize animal data indicating that stress negatively affects mesocorticolimbic dopaminergic pathways critically implicated in incentive motivation and reinforcement learning. In the last section, we provide a synthesis of these four literatures, present initial evidence consistent with our model, and discuss directions for future research.
The authors' abstract, as published at the source. Annual Review of Clinical Psychology, 2014 · DOI ↗
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Field: Cellular and Molecular Neuroscience
Cellular and Molecular NeuroscienceNeuroscience