摘要
目的:研究桂皮醛对白细胞与血管内皮细胞黏附影响的分子机制,探讨其促进皮肤创伤愈合的机制。方法:虎红染色法观察桂皮醛高(10mg/L)、中(5 mg/L)、低(2.5 mg/L)浓度对人中性粒细胞(polymorphonuclear,PMN)与肿瘤坏死因子(tumor necrosis factor,TNF)诱导的人脐静脉内皮细胞(human umbilical vein endothelial cell,HUVEC)黏附的影响;荧光免疫细胞化学法观察桂皮醛对HUVEC表面细胞间黏附分子-1(intercellular adhesion molecule-1,ICAM-1)、血管细胞黏附分子-1(vascular cell adhesion molecule-1,VCAM-1)和CD_(44)表达的影响。结果:桂皮醛和TNF共同作用HUVEC 4 h后,高浓度桂皮醛能明显抑制HUVEC与PMN黏附(P<0.05),能明显抑制HUVEC表面VCAM-1表达(P<0.01)。中浓度桂皮醛能明显抑制HUVEC表面ICAM-1和VCAM-1表达(P<0.05)。各浓度桂皮醛对HUVEC表面CD_(44)表达未表现明显作用。桂皮醛和TNF共同作用HUVEC 12 h后,桂皮醛未表现以上作用。结论:桂皮醛作用早期通过降低TNF诱导的HUVEC表面黏附分子的表达,抑制白细胞与血管内皮细胞的黏附,从而抑制过度的炎症反应来促进创伤愈合。
AIM: To observe the inhibition effects and molecular mechanisms of cinnamaldehyde on the adhesion of polymorphonuclear(PMN) to hu- man umbilical vein endothelial cells (HUVEC), and to explore the mechanism of cinnamaldehyde on promoting skin wound healing. METHODS: The effect of cinnamaldehyde on HUVEC and human pe- ripheral PMN cell activity were observed by MTT and trypan-blue assay, repectively. The effect of cinnamaldehyde at high ( 10 mg/L ), medium ( 5 mg/L)and low(2.5mg/L)concentration on the adhesion of PMN to HUVEC primed by TNF were observed by Rose Bengal Stainning. Expressions of ICAM-1, VCAM-1and CD44 on HUVEC were meas- ured by fluorescent-immunocytochemistry assay. RESULTS: High dose of cinnamaldehyde decreased PMN-HUVEC adhesion at 4 h after treated by cinna- maldehyde and TNF(P 〈 0.05 ), and showed lower level of VCAM-1 on HUVEC (P 〈 0.01 ). Medium dose of cinnamaldehyde decreased the level of ICAM-1 and VCAM-1 on HUVEC (P 〈 0.05). There was no statistic difference for cinnamaldehyde on the level of CD44 on HUVEC. CONCLUSION: Cinnamaldehyde may inhibit the adhesion of PMN to HUVEC by decreasing the expression of adhesion molecules on HUVEC, therefore inhibiting excessive inflammatory response.
出处
《中国临床药理学与治疗学》
CAS
CSCD
2017年第1期43-47,共5页
Chinese Journal of Clinical Pharmacology and Therapeutics
基金
国家自然科学基金项目(81273768,81403270,81403409)
关键词
创伤愈合
桂皮醛
黏附分子
人脐静脉内皮细胞
wound healing
cinnamaldehyde
adhesion molecules
human umbilical vein endothe-lial cells (HUVEC)