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

被引:31
作者
Liao, Hsien-Yin [1 ]
Lin, Yi-Wen [2 ,3 ]
机构
[1] China Med Univ, Sch Postbaccalaureate Chinese Med, Coll Chinese Med, Taichung 40402, Taiwan
[2] China Med Univ, Grad Inst Acupuncture Sci, Coll Chinese Med, 91 Hsueh Shih Rd, Taichung 40402, Taiwan
[3] China Med Univ, Chinese Med Res Ctr, Taichung 40402, Taiwan
来源
AMERICAN JOURNAL OF CHINESE MEDICINE | 2021年 / 49卷 / 06期
关键词
TRPV1; Acupuncture; Chronic Pain; Depression; Inflammation; Prefrontal Cortex; MEDIAL PREFRONTAL CORTEX; ACUPUNCTURE; ACTIVATION; STRESS; RAT; EXPRESSION; PLASTICITY; RELEASE; MICE;
D O I
10.1142/S0192415X2150066X
中图分类号
R [医药、卫生];
学科分类号
10 ;
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 Ca2+ 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(-/-) 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.
引用
收藏
页码:1417 / 1435
页数:19
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