Oxidative Stress in Depression: The Link with the Stress Response, Neuroinflammation, Serotonin, Neurogenesis and Synaptic Plasticity
Оксидативный стресс при депрессии: связь со стрессовым ответом, нейровоспалением, серотонином, нейрогенезом и синаптической пластичностью
2023-02-13
SCID: 54.1/f6ugnf99
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depressionneuroinflammationoxidative stressserotonergic pathwayssynaptic plasticity
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Abstract (AI)
Depression is a prevalent, complex, and highly debilitating disease. The full comprehension of this disease is still a global challenge. Indeed, relapse, recurrency, and therapeutic resistance are serious challenges in the fight against depression. Nevertheless, abnormal functioning of the stress response, inflammatory processes, neurotransmission, neurogenesis, and synaptic plasticity are known to underlie the pathophysiology of this mental disorder. The role of oxidative stress in disease and, particularly, in depression is widely recognized, being important for both its onset and development. Indeed, excessive generation of reactive oxygen species and lack of efficient antioxidant response trigger processes such as inflammation, neurodegeneration, and neuronal death. Keeping in mind the importance of a detailed study about cellular and molecular mechanisms that are present in depression, this review focuses on the link between oxidative stress and the stress response, neuroinflammation, serotonergic pathways, neurogenesis, and synaptic plasticity's imbalances present in depression. The study of these mechanisms is important to lead to a new era of treatment and knowledge about this highly complex disease.
Key Findings
1
Depression is associated with abnormal stress-response functioning, inflammatory processes, serotonergic neurotransmission, neurogenesis, and synaptic plasticity.
2
Oxidative imbalance may promote neuroinflammation, neurodegeneration, and neuronal death, contributing to depression’s pathophysiology.
3
Oxidative stress is implicated in both the onset and progression of depression, through excessive reactive oxygen species generation and inadequate antioxidant defenses.
4
The review examines mechanistic links between oxidative stress and dysregulation of stress responses, neuroinflammation, serotonin pathways, neurogenesis, and synaptic plasticity.
5
Understanding these interconnected cellular and molecular mechanisms may support development of improved treatments for relapse, recurrence, and therapeutic resistance in depression.
Research Object
Depression
Research Subject
The links between oxidative stress and imbalances in the stress response, neuroinflammation, serotonergic pathways, neurogenesis, and synaptic plasticity
Publication Details
Publication Date
2023-02-13
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