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从环氧化酶和5-脂氧化酶途径探讨虎杖痛风颗粒的抗炎机制
引用本文:王一飞,吴文静,张明,周敏,李斌. 从环氧化酶和5-脂氧化酶途径探讨虎杖痛风颗粒的抗炎机制[J]. 中西医结合学报, 2009, 7(10): 963-968. DOI: 10.3736/jcim20091010
作者姓名:王一飞  吴文静  张明  周敏  李斌
作者单位:上海中医药大学岳阳中西医结合医院痛风专科,上海,200437
基金项目:上海市中医临床优势专病建设项目,上海市申康医院发展中心市级医院中医药验方临床评价项目,国家中医药管理局"十一五"重点专病建设项目 
摘    要:目的:观察虎杖痛风颗粒对环氧化酶(cyclooxygenase,COX)和5-脂氧化酶(5-lipoxygenase,5-LOX)活性的影响,探讨虎杖痛风颗粒抗炎的可能机制。方法:健康志愿者全血标本加入钙离子载体A23187予以刺激,以阿司匹林为对照,通过酶联免疫吸附测定(enzyme-linked immunosorbent assay,ELISA)法检测血栓素B2(thromboxane B2,TXB2)含量考察不同浓度的虎杖痛风颗粒溶液对COX-1活性的影响;健康志愿者全血经阿司匹林灭活COX-1后,予脂多糖(lipopolysaccharide,LPS)刺激后,以塞来昔布为对照,通过ELISA检测前列环素I2(prostaglandin I2,PGI2)含量考察不同浓度虎杖痛风颗粒溶液对COX-2活性的影响;大鼠皮下植入含0.5%花生四烯酸溶液的棉球,收集渗液中的多形核白细胞(polymorphonuclear leukocyte,PMN),采用反相高效液相色谱法测定白细胞三烯B4(leukotriene B4,LTB4)含量考察不同剂量虎杖痛风颗粒对5-LOX活性的影响。结果:低浓度虎杖痛风颗粒组TXB2浓度较高浓度虎杖痛风颗粒组和阿司匹林组升高(P<0.05);高、低浓度虎杖痛风颗粒组PGI2浓度较塞来昔布组明显升高(P<0.05),高、低浓度虎杖痛风颗粒组之间比较,差异无统计学意义(P>0.05);空白对照组LTB4含量较高、低剂量虎杖痛风颗粒组和地塞米松组高(P<0.05)。结论:虎杖痛风颗粒能通过抑制COX和5-LOX的活性减少TXB2、PGI2和LTB4等炎症介质的释放。

关 键 词:痛风性关节炎  虎杖痛风颗粒  环氧化酶  5-脂氧化酶

Inhibiting cyclooxygenase and 5-lipoxygenase activities is an anti-inflammatory mechanism of Huzhang Gout Granule
Yi-fei WANG,Wen-jing WU,Ming ZHANG,Min ZHOU,Bin LI. Inhibiting cyclooxygenase and 5-lipoxygenase activities is an anti-inflammatory mechanism of Huzhang Gout Granule[J]. Journal of Chinese integrative medicine, 2009, 7(10): 963-968. DOI: 10.3736/jcim20091010
Authors:Yi-fei WANG  Wen-jing WU  Ming ZHANG  Min ZHOU  Bin LI
Affiliation:(Gout Clinic, Yueyang Hospital of Integrated Traditional Chinese and Western Medicine, Shanghai University of Traditional Chinese Medicine, Shanghai 200437, China)
Abstract:Objective: To observe the effects of Huzhang Gout Granule (HZGG), a compound traditional Chinese herbal medicine, on cyclooxygenase (COX) and 5-lipoxygenase (5-LOX) activities, the two important oxidases in the course of inflammation, so as to investigate the possible anti-inflammatory mechanism of HZGG.
Methods: After stimulating the blood sample of healthy volunteer with calcium ionophore A23187, concentration of thromboxane B2 (TXB2) in the healthy volunteer’s blood was detected by enzyme-linked immunosorbent assay (ELISA) to observe the effects of HZGG at low- and high-dose on the activity of COX-1, with aspirin as control drug. The concentration of prostaglandin I2 (PGI2) in the healthy volunteer’s blood sample, in which aspirin was added to destroy activity of COX-1 beforehand and which was stimulated with lipopolysaccharide, was detected by ELISA method to observe the effects of HZGG on the activity of COX-2, with celecoxib as control drug. In the animal experiment, 40 rats were implanted with sponges soaking in 0.5% arachidonic acid solution in the back to induce inflammatory effusion. Content of leukotriene B4 (LTB4) in the polymorphonuclear leukocytes (PMNs) from the inflammatory effusions was detected with reversed-phase high-performance liquid chromatography (RP-HPLC) to observe the impacts of different doses of HZGG on the activity of 5-LOX, with dexamethasone as control drug.
Results: The concentration of TXB2 in the low-dose HZGG group was higher than those in the high-dose HZGG group and the aspirin group (P〈0.05). The concentrations of PGI2 in the low- and high-dose HZGG groups were higher than that in the celecoxib group (P〈0.05), but there was no significant difference between the low-dose HZGG group and the high-dose HZGG group (P〉0.05). The content of LTB4 in the blank control group was higher than those in the low-dose HZGG group, the high-dose HZGG group or the dexamethasone group (P〈0.05).
Conclusion: HZGG can reduce the releasing of inflammatory mediators, such as TXB2, PGI2 and LTB4, by inhibiting the activities of COX and 5-LOX.
Keywords:acute gouty arthritis  Huzhang Gout Granule  cyclooxygenase  5-lipoxygenase
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