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Demonstrates reduced chronic pain and depression comorbidity in mice using eicosapentaenoic acid, suggesting new treatment strategies.
BACKGROUND: Fibromyalgia is a frequently treatment-refractory chronic musculoskeletal pain disorder that often results in clinical depression; however, the role of neuroinflammatory signaling in comorbid depression remains unclear, including the contributions of anti-inflammatory omega-3 fatty acids like eicosapentaenoic acid (EPA). METHODS: This study examined the efficacy of EPA ingestion for reducing chronic pain and depression comorbidity (CPDC) in a mouse model established using intermittent cold stress. RESULTS: gene knockout mice. CONCLUSION: This demonstration that oral EPA can prevent CPDC by inhibiting neuroinflammatory pathways could facilitate improved treatment strategies for CPDC.
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Ho et al. (2026) studied this question.
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