Lee Mu Hong, Lee Jeong Min, Jun Sung Hoon, Ha Chul Gyu, Lee Seung-Ha, Kim Nam Wook, Lee Jun Ho, Ko Na Young, Mun Se Hwan, Park Seung Hwa, Kim Bo Kyung, Her Erk, Kim Young Mi, Choi Wahn Soo
Life Science R&D Center, Sinil Pharmaceutical Co., Ltd., Chungju 380-862, Korea.
J Pharm Pharmacol. 2007 Jan;59(1):123-30. doi: 10.1211/jpp.59.1.0016.
In this study, we aimed to investigate the anti-inflammatory activity, antinociceptive activity and the action mechanism of Trachelospermi caulis extract. The anti-inflammatory effects were investigated using arachidonic acid, 12-O-tetradecanoylphorbol 13-acetate or carrageenan-induced oedema assays. Antinociceptive activity, using the acetic acid-induced writhing model, was also tested in mice. The extract exhibited dose-dependent and significant (P<0.05 at 100-400 mg kg-1) anti-inflammatory and antinociceptive activity in the animals. To further understand the mechanism of activity, we investigated whether the extract inhibited the expression of inducible nitric oxide synthase (iNOS), the production of nitric oxide (NO) and the expression of TNF-alpha from murine macrophage RAW 264.7 cells. Similar to the in-vivo activity, the iNOS expression, NO production and TNF-alpha expression were found to be dose dependent and significantly suppressed by the extract through the inhibition of the p38 MAP kinase/NF-kappaB pathway. Taken together, the results presented here suggest that T. caulis extract may be useful for the treatment of various inflammatory diseases.
在本研究中,我们旨在研究络石藤提取物的抗炎活性、镇痛活性及其作用机制。使用花生四烯酸、12 - O - 十四酰佛波醇 - 13 - 乙酸酯或角叉菜胶诱导的水肿试验来研究其抗炎作用。还在小鼠中使用乙酸诱导的扭体模型测试了镇痛活性。该提取物在动物中表现出剂量依赖性且显著(100 - 400 mg kg-1时P<0.05)的抗炎和镇痛活性。为了进一步了解其活性机制,我们研究了该提取物是否抑制小鼠巨噬细胞RAW 264.7细胞中诱导型一氧化氮合酶(iNOS)的表达、一氧化氮(NO)的产生以及肿瘤坏死因子 - α(TNF - α)的表达。与体内活性相似,发现iNOS表达、NO产生和TNF - α表达呈剂量依赖性,并且该提取物通过抑制p38丝裂原活化蛋白激酶/核因子 - κB途径对其有显著抑制作用。综上所述,此处呈现的结果表明络石藤提取物可能对治疗各种炎症性疾病有用。