Liu Fang, Fang Jian-qiao, Shao Xiao-mei
Department of Acu-moxibusion, Zhejiang Hospital of Integrated Chinese & Western Medicine, Hangzhou 310003, China.
Zhen Ci Yan Jiu. 2009 Jun;34(3):159-62.
To observe the effect of electroacupuncture (EA) on changes of cyclooxygenase (COX)-2 mRNA and protein expression after inflammation occurrence at the back by application of human recombinant IL-1beta (hr IL-Ibeta) plus air-pouch in rats, so as to analyze the relativity between EA-induced changes of COX-2 expression and proinflammatory cytokines regulative pathway.
Ninety female Wistar rats were randomized into control, model, and EA groups with 30 cases in each. Inflammatory model was established by subcutaneous implantation of a sterilized hollow teflon cylinder (sac, 1.5 mi in volume) at the back and intrasaccal injection of hr IL-1beta (10 ng/ml). EA (2 Hz, 1 mA) was immediately applied to "Quchi" (LI 11) for 30 min. Exudate in the sac was withdrawn at various intervals after hr IL-1beta-injection for assaying COX-2 mRNA expression with RT-PCR and protein expression with Western Blotting.
In comparison with control group, one hour (h) after hr IL-1beta-injection, COX-2 mRNA and protein expression levels were up-regulated significantly in model group (P < 0.01); while compared to model group, COX-2 mRNA and protein expression levels in EA group were down-regulated considerably (P < 0.05). 5 h and 24 h after hr IL-1beta-injection, COX-2 mRNA expression in model and EA groups was significantly higher than that in control group (P < 0.01), and no significant differences were found between model and EA groups in COX-2 mRNA expression levels (P > 0.05). On the contrary, 5 h after administration of hr IL-1beta, COX-2 protein expression in model group was significantly higher than that in control group (P < 0.05). On the 24 h after hr Ibeta-1beta-injection, no significant differences were found in COX-2 protein expression levels among control, model and EA groups (P > 0.05).
EA can effectively suppress hr IL-1beta-injection induced up-regulation of COX-2 mRNA and protein expression in the rats, suggesting a close relativity between the regulation of proinflammatory cytokines and EA-induced inhibition of COX-2 mRNA and protein expression.
观察电针对大鼠背部应用人重组白细胞介素-1β(hr IL-1β)加气囊致炎后环氧化酶(COX)-2 mRNA和蛋白表达变化的影响,分析电针诱导的COX-2表达变化与促炎细胞因子调节途径之间的相关性。
将90只雌性Wistar大鼠随机分为对照组、模型组和电针组,每组30只。通过在背部皮下植入无菌空心聚四氟乙烯圆柱体(气囊,体积1.5 ml)并向囊内注射hr IL-1β(10 ng/ml)建立炎症模型。立即将电针(2 Hz,1 mA)施加于“曲池”(LI 11)30分钟。在注射hr IL-1β后的不同时间间隔抽取囊内渗出液,用逆转录-聚合酶链反应(RT-PCR)检测COX-2 mRNA表达,用蛋白质印迹法检测蛋白表达。
与对照组相比,注射hr IL-1β后1小时,模型组COX-2 mRNA和蛋白表达水平显著上调(P < 0.01);与模型组相比,电针组COX-2 mRNA和蛋白表达水平显著下调(P < 0.05)。注射hr IL-1β后5小时和24小时,模型组和电针组COX-2 mRNA表达均显著高于对照组(P < 0.01),模型组和电针组COX-2 mRNA表达水平无显著差异(P > 0.05)。相反,注射hr IL-1β后5小时,模型组COX-2蛋白表达显著高于对照组(P < 0.05)。注射hr IL-1β后24小时,对照组、模型组和电针组COX-2蛋白表达水平无显著差异(P > 0.05)。
电针能有效抑制注射hr IL-1β诱导的大鼠COX-2 mRNA和蛋白表达上调,提示促炎细胞因子调节与电针诱导的COX-2 mRNA和蛋白表达抑制之间存在密切相关性。