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邻甲氧基桂皮醛对IL-1刺激脑微血管内皮细胞COX活性及PGE2释放的影响
引用本文:郭建友,杨元宵,赵保胜,刘洪斌,李兰芳,马悦颖,郭淑英,霍海如,姜廷良. 邻甲氧基桂皮醛对IL-1刺激脑微血管内皮细胞COX活性及PGE2释放的影响[J]. 中国中药杂志, 2006, 31(13): 1087-1090
作者姓名:郭建友  杨元宵  赵保胜  刘洪斌  李兰芳  马悦颖  郭淑英  霍海如  姜廷良
作者单位:1. 中国中医科学院,中药研究所,北京,100700;中国科学院,心理研究所,北京,100101
2. 浙江中医学院,浙江,杭州,310053
3. 中国中医科学院,中药研究所,北京,100700
摘    要:目的:观察桂枝汤有效部位A分离的邻甲氧基桂皮醛对发热相关的环氧酶(COX)和前列腺素E2(PGE2)的影响。方法:建立大鼠脑微血管内皮细胞(rCMEC)培养,进行Ⅷ因子相关抗原鉴定。待细胞生长至融合状态后加入不同含量的邻甲氧基桂皮醛(12.5,25,50,100,200 μg·mL-1)孵育3 h,之后以30 ng·mL-1的IL-1刺激12 h。ELISA方法检测细胞培养液中PGE2的含量及细胞内COX-1和COX-2的活性。结果:Ⅷ因子抗体免疫组化染色可见90%以上的培养细胞呈阳性,确认为rCMEC。暴露于30 ng·mL-1 IL-1后,rCMEC内COX-2活性及释放的PGE2量显著增加,COX-1活性变化无统计学差异。加入不同含量的邻甲氧基桂皮醛后,随含量增加可下调COX-1,COX-2活性及PGE2量,且呈剂量依赖关系;至含量为200 μg·mL-1时,COX-2活性及释放的PGE2与IL-1单独作用组相比均有显著性差异,COX-1活性虽有所降低,但无统计学上的显著差异。结论:邻甲氧基桂皮醛能下调IL-1刺激rCMEC释放升高的PGE2,作用机制可能与抑制COX-2活性有关。

关 键 词:邻甲氧基桂皮醛  脑微血管内皮细胞  白介素1  环氧酶  前列腺素E
文章编号:1001-5302(2006)13-1087-04
收稿时间:2005-11-21
修稿时间:2005-11-21

Effect of 2-methoxycinnamaldehyde on activity of COX and PGE2release in cerebral microvascular endothelial cells stimulated by IL-1
GUO Jian-you ; YANG Yuan-xiao ; ZHAO Bao-sheng ; LIU Hong-bin ; LI Lan-fang ; MA Yue-ying ; GUO Shu-ying ; HUO Hai-ru ; JIANG Ting-liang. Effect of 2-methoxycinnamaldehyde on activity of COX and PGE2release in cerebral microvascular endothelial cells stimulated by IL-1[J]. China Journal of Chinese Materia Medica, 2006, 31(13): 1087-1090
Authors:GUO Jian-you    YANG Yuan-xiao    ZHAO Bao-sheng    LIU Hong-bin    LI Lan-fang    MA Yue-ying    GUO Shu-ying    HUO Hai-ru    JIANG Ting-liang
Affiliation:Institute of Chinese Materia Medica, China Academy of Chinese Medical Sciences, Beijing.
Abstract:OBJECTIVE: To observe the effect of 2-methoxycinnamaldehyde (isolated from fraction A of Guizhi Tang) on activity of COX and PGE2 release in rat cerebral microvascular endothelial cells (rCMEC) stimulated by IL-1. METHOD: rCMEC were cultured, and identified by immunohistochemistry for von Willebrand factor (VIII factor, a marker for all endothelial cells) in cytoplasm of the cells. Different concentrations of 2-methoxycinnamaldehyde were added respectively and incubated for 3 hours, then stimulated for another 12 hours by IL-1. Activities of COX-1 and COX-2 in rCMEC, and production of PGE2 in the conditioned media were measured by ELISA. RESULT: Positive immunostaining for VIII factor was present diffusely in the cytoplasm of > 90% rCMEC. After being exposed to 30 ng x mL(-1) IL, the activity of COX-2 in rCMEC and the production of PGE2 in conditioned media were higher than those of control group, while there was no difference on activity of COX-1 in the two groups. 2-methoxycinnamaldehyde could down-regulate them in concentration-dependently, and significant differences on the activity of COX-2 and amount of PGE2 were showed in 200 microg x mL(-1) concentration. CONCLUSION: 2-methoxycinnamaldehyde can affect the PGE2 release in rCMEC induced by IL-1, which might be related with its inhibition on the activity of COX-2.
Keywords:2-methoxycinnamaldehyde   cerebral microvascular endothelial cells   IL-1   COX   PGE
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