Department of Neurobiology and Key Laboratory of Neurological Diseases of Hubei Province, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Eur J Pain. 2012 May;16(5):624-35. doi: 10.1002/j.1532-2149.2011.00055.x. Epub 2011 Dec 19.
Endogenous cannabinoids and peripheral cannabinoid CB2 receptors (CB2Rs) are involved in the antinociceptive effect of electroacupuncture (EA) on inflammatory pain. However, it is not clear how CB2R activation contributes to the antinociceptive effect of EA. The major proinflammatory cytokines, such as tumour necrosis factor-α (TNF-α), interleukin-1β (IL-1β) and IL-6, are involved in inflammatory pain. Here we determined the effects of CB2R activation and EA on the expression level of IL-1β, IL-6 and TNF-α in inflamed skin tissues. Inflammatory pain was induced by injection of complete Freund's adjuvant into the left hindpaw of rats. Thermal hyperalgesia was tested with a radiant heat stimulus, and mechanical allodynia was quantified using von Frey filaments. The mRNA and protein levels of IL-1β, IL-6 and TNF-α in inflamed skin tissues were measured using real-time polymerase chain reaction and Western blot, respectively. Local injection of the selective CB2R agonist AM1241 or EA applied to GB30 and GB34 significantly reduced thermal hyperalgesia and mechanical allodynia induced by tissue inflammation. The specific CB2R antagonist AM630 significantly attenuated the antinociceptive effect of EA. Furthermore, EA or AM1241 treatment significantly decreased the mRNA and protein levels of IL-1β, IL-6 and TNF-α in inflamed skin tissues. In addition, pretreatment with AM630 significantly reversed the inhibitory effect of EA on these cytokine levels in inflamed skin tissues. Our results suggest that EA reduces inflammatory pain and proinflammatory cytokines in inflamed skin tissues through activation of CB2Rs.
内源性大麻素和外周大麻素 CB2 受体(CB2Rs)参与电针(EA)对炎性疼痛的镇痛作用。然而,CB2R 激活如何有助于 EA 的镇痛作用尚不清楚。主要的促炎细胞因子,如肿瘤坏死因子-α(TNF-α)、白细胞介素-1β(IL-1β)和 IL-6,参与了炎性疼痛。在这里,我们确定了 CB2R 激活和 EA 对炎性皮肤组织中 IL-1β、IL-6 和 TNF-α表达水平的影响。通过向大鼠左后足注射完全弗氏佐剂诱导炎性疼痛。使用辐射热刺激测试热痛觉过敏,并用冯弗雷尔细丝量化机械性痛觉过敏。使用实时聚合酶链反应和 Western blot 分别测量炎性皮肤组织中 IL-1β、IL-6 和 TNF-α的 mRNA 和蛋白水平。局部注射选择性 CB2R 激动剂 AM1241 或应用于 GB30 和 GB34 的 EA 显著减轻组织炎症引起的热痛觉过敏和机械性痛觉过敏。特异性 CB2R 拮抗剂 AM630 显著减弱 EA 的镇痛作用。此外,EA 或 AM1241 处理显著降低了炎性皮肤组织中 IL-1β、IL-6 和 TNF-α的 mRNA 和蛋白水平。此外,AM630 的预处理显著逆转了 EA 对炎性皮肤组织中这些细胞因子水平的抑制作用。我们的结果表明,EA 通过激活 CB2Rs 减轻炎性疼痛和炎性皮肤组织中的促炎细胞因子。