The Third Clinical Medical College, Zhejiang Chinese Medical University, 548 Binwen Road, Binjiang District, Hangzhou City, Zhejiang Province 310053, China.
Evid Based Complement Alternat Med. 2012;2012:568273. doi: 10.1155/2012/568273. Epub 2011 Aug 8.
Activation of mitogen-activated protein kinases (MAPKs), especially p38 MAPK, plays an important role in the development of central sensitization related to persistent inflammatory pain. Electroacupuncture (EA) is well known to relieve persistent inflammatory pain. However, little is known about relationship between EA and p38 MAPK. Inflammatory pain rat model was induced by intraplantar injection of complete Freund's adjuvant (CFA). Male adult SD rats were randomly divided into the saline group, CFA group, and CFA + EA group. EA (constant saquare wave, 2 Hz and 100 Hz alternating frequencies, intensities ranging from 1 to 2 mA) was applied to bilateral "Zusanli" (ST 36) and "Kunlun" acupoints (BL 60) for 30 min, once per day. The paw edema and paw withdrawal threshold (PWT) were measured at preinjection and days postinjection 1, 3, and 14. Spinal p-p38MAPK- immunoreactivty (p-p38MAPK-IR) cells were detected by immunohistochemistry at postinjection day 3 and 14. EA significantly inhibited paw edema at postinjection days 14 and increased PWT at postinjection days 3 and 14. Moreover, the increasing number of spinal p-p38MAPK-IR cells which was induced by CFA injection was suppressed by EA stimulation. These results indicate that anti-inflammatory and analgesic effect of EA might be associated with its inhibition of spinal p38 MAPK activation and thereby provide a potential mechanism for the treatment of inflammatory pain by EA.
丝裂原活化蛋白激酶(MAPKs)的激活,尤其是 p38 MAPK 的激活,在与持续性炎症痛相关的中枢敏化的发展中起着重要作用。电针(EA)已被证明可缓解持续性炎症痛。然而,EA 与 p38 MAPK 之间的关系知之甚少。通过足底注射完全弗氏佐剂(CFA)诱导炎症痛大鼠模型。雄性成年 SD 大鼠随机分为盐水组、CFA 组和 CFA+EA 组。EA(恒方波,2 Hz 和 100 Hz 交替频率,强度为 1 至 2 mA)应用于双侧“足三里”(ST36)和“昆仑”(BL60)穴位 30 分钟,每天一次。在注射前和注射后第 1、3 和 14 天测量足肿胀和足撤回阈值(PWT)。在注射后第 3 和第 14 天通过免疫组织化学检测脊髓 p-p38MAPK-免疫反应性(p-p38MAPK-IR)细胞。EA 显著抑制注射后第 14 天的足肿胀,并增加注射后第 3 和第 14 天的 PWT。此外,CFA 注射引起的脊髓 p-p38MAPK-IR 细胞数量的增加被 EA 刺激抑制。这些结果表明,EA 的抗炎和镇痛作用可能与其抑制脊髓 p38 MAPK 激活有关,从而为 EA 治疗炎症痛提供了一种潜在机制。