Electroacupuncture Attenuates Chronic Inflammatory Pain and Depression Comorbidity through Transient Receptor Potential V1 in the Brain

TRPV1型 慢性疼痛 行为绝望测验 电针 瞬时受体电位通道 医学 前额叶皮质 导水管周围灰质 开阔地 内科学 炎症 痛觉过敏 神经科学 内分泌学 受体 抗抑郁药 药理学 针灸科 伤害 心理学 中枢神经系统 海马体 精神科 病理 中脑 替代医学 认知
作者
Hsien-Yin Liao,Yi‐Wen Lin
出处
期刊:The American Journal of Chinese Medicine [World Scientific]
卷期号:49 (06): 1417-1435 被引量:34
标识
DOI:10.1142/s0192415x2150066x
摘要

Chronic pain is one of the highest costs in clinical therapy, often appearing comorbid with depression. They present with overlapping clinical conditions and common pathological pathways especially in neuroinflammation, both of which can be reversed by electroacupuncture (EA). Transient receptor potential V1 receptor (TRPV1) is a Ca[Formula: see text] permeable ion channel that responds to brain inflammation and has a known role in the development of chronic pain and depression. Here, we investigate the role of TRPV1 and its related molecules in a mouse model of inflammation-induced chronic pain and depression using Complete Freund's adjuvant (CFA). We measured inflammatory mediators in plasma and evaluated the TRPV1 signaling pathway in the medial prefrontal cortex (mPFC), hypothalamus, and periaqueductal gray (PAG) of the mouse brain. Mechanical and thermal hyperalgesia as well as depressive-like behaviors were induced using the open field test and forced swimming test. Therapeutic effects were observed in EA and Trpv1[Formula: see text] mice in measures of chronic pain and depression. Inflammatory mediators induced by CFA injection were attenuated by EA and Trpv1 deletion. TRPV1 and downstream molecules were significantly decreased in the mPFC, hypothalamus, and PAG of mice, effects which were reversed by EA and Trpv1 knockout. We provide novel evidence that these inflammatory mediators modulate the TRPV1 signaling pathway and suggest new potential therapeutic targets for chronic pain and depression.
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