Wang Hong-Ling, Li Yu-Xiang, Niu Ya-Ting, Zheng Jie, Wu Jing, Shi Guang-Jiang, Ma Lin, Niu Yang, Sun Tao, Yu Jian-Qiang
Department of Pharmacology, School of Pharmacy, Ningxia Medical University, Yinchuan, 750004, China.
College of Nursing, Ningxia Medical University, Yinchuan, 750004, China.
Inflammation. 2015 Dec;38(6):2269-78. doi: 10.1007/s10753-015-0212-3.
The present study aimed to investigate the potential anti-inflammatory and anti-nociceptive activities of glycyrrhizin (GL) in mice and to explore the possible related mechanisms. Xylene-induced ear edema, carrageenan-induced paw edema and acetic acid-induced vascular permeability test were used to investigate the anti-inflammatory activities of GL in mice. Anti-nociceptive effects of GL were assessed by using acetic acid-induced writhing, hot plate test and formalin test, as well as evaluation of spontaneous locomotor activity and motor performance. The mRNA expression of pro-inflammatory cytokines (such as TNF-α, IL-6 and iNOS) and the protein expression of cyclooxygenase-2 (COX-2) were explored by using real-time fluorogenic PCR and Western blot, respectively. The results showed that GL significantly reduced xylene-induced ear edema, carrageenan-induced paw edema, and acetic acid-induced vascular permeation. Additionally, GL significantly inhibited the nociceptions induced by acetic acid and formalin. However, the nociceptions could not be decreased by GL in the hot plate test, and GL did not affect spontaneous locomotor activity and motor performance. The expression levels of TNF-α, IL-6, iNOS and COX-2 were significantly downregulated by GL. In conclusion, GL exerts significant anti-inflammatory and analgesic activities by attenuating the expression levels of TNF-α, IL-6, iNOS and COX-2.
本研究旨在探讨甘草酸(GL)在小鼠体内的潜在抗炎和抗伤害感受活性,并探索其可能的相关机制。采用二甲苯诱导的耳肿胀、角叉菜胶诱导的足肿胀和乙酸诱导的血管通透性试验来研究GL对小鼠的抗炎活性。通过乙酸诱导的扭体试验、热板试验和福尔马林试验评估GL的抗伤害感受作用,并评估自发运动活性和运动能力。分别采用实时荧光定量PCR和蛋白质印迹法检测促炎细胞因子(如TNF-α、IL-6和诱导型一氧化氮合酶)的mRNA表达以及环氧化酶-2(COX-2)的蛋白表达。结果显示,GL显著减轻了二甲苯诱导的耳肿胀、角叉菜胶诱导的足肿胀以及乙酸诱导的血管通透性。此外,GL显著抑制了乙酸和福尔马林诱导的伤害感受。然而,在热板试验中GL未能降低伤害感受,且GL不影响自发运动活性和运动能力。GL显著下调了TNF-α、IL-6、诱导型一氧化氮合酶和COX-2的表达水平。总之,GL通过降低TNF-α、IL-6、诱导型一氧化氮合酶和COX-2的表达水平发挥显著的抗炎和镇痛活性。