中国医师杂志
中國醫師雜誌
중국의사잡지
JOURNAL OF CHINESE PHYSICIAN
2011年
5期
621-623
,共3页
李云峰%蔡业平%张圣岸%戴新贵
李雲峰%蔡業平%張聖岸%戴新貴
리운봉%채업평%장골안%대신귀
肝素,低分子量/药理学%脓毒症/代谢%内皮细胞/代谢/药物作用%蛋白质C/代谢%受体,PAR-1/代谢
肝素,低分子量/藥理學%膿毒癥/代謝%內皮細胞/代謝/藥物作用%蛋白質C/代謝%受體,PAR-1/代謝
간소,저분자량/약이학%농독증/대사%내피세포/대사/약물작용%단백질C/대사%수체,PAR-1/대사
Heparin,low-molecular-weight/PD%Sepsis/ME%Endothelial cells/ME/DE%Protein C/ME%Receptor,PAR-1/ME
目的 观察低分子肝素(LMWH)对脓毒症大鼠腹主动脉内皮细胞(VEC)蛋白C受体(EPCR)和蛋白酶活化受体1(PAR1)表达的影响.方法 采用组织贴块法培养24只Wister大鼠腹主动脉VEC,1:3传代至第4代,分为对照组(n=6)、脓毒症组(LPS 1 μg/ml,n=6)、LMWH组(LPS 1 μg/ml+LMWH 5 μg/ml,n=6).分别在第1、3、5天采用流式细胞术(FCM)检测VEC表面的EPCR和PAR1的表达.结果 脓毒症组EPCR和PAR1的表达各时间点均较对照组有明显下降(P<0.05或P<0.01),以第5天最为明显(26.53±7.21 vs 39.26±2.62,q=6.45,P<0.01;53.21±15.10 vs 86.54±11.34,q=6.94,P<0.01).LMWH组EPCR和PAR1的表达各时间点均高于脓毒症组(P<0.05);与对照组比较,EPCR在第1天仍有明显降低(40.86±1.63 vs 45.41±2.82,q=3.51,P<0.05),但第3、5天接近对照组水平(41.20±3.32 vs 42.83±2.66,P>0.05;39.23±3.33 vs 39.26±2.62,P>0.05),PAR1各时间点与对照组比较差异均无统计学意义(P>0.05).结论 LMWH能有效改善脓毒症内皮细胞EPCR和PAR1表达抑制的状态.
目的 觀察低分子肝素(LMWH)對膿毒癥大鼠腹主動脈內皮細胞(VEC)蛋白C受體(EPCR)和蛋白酶活化受體1(PAR1)錶達的影響.方法 採用組織貼塊法培養24隻Wister大鼠腹主動脈VEC,1:3傳代至第4代,分為對照組(n=6)、膿毒癥組(LPS 1 μg/ml,n=6)、LMWH組(LPS 1 μg/ml+LMWH 5 μg/ml,n=6).分彆在第1、3、5天採用流式細胞術(FCM)檢測VEC錶麵的EPCR和PAR1的錶達.結果 膿毒癥組EPCR和PAR1的錶達各時間點均較對照組有明顯下降(P<0.05或P<0.01),以第5天最為明顯(26.53±7.21 vs 39.26±2.62,q=6.45,P<0.01;53.21±15.10 vs 86.54±11.34,q=6.94,P<0.01).LMWH組EPCR和PAR1的錶達各時間點均高于膿毒癥組(P<0.05);與對照組比較,EPCR在第1天仍有明顯降低(40.86±1.63 vs 45.41±2.82,q=3.51,P<0.05),但第3、5天接近對照組水平(41.20±3.32 vs 42.83±2.66,P>0.05;39.23±3.33 vs 39.26±2.62,P>0.05),PAR1各時間點與對照組比較差異均無統計學意義(P>0.05).結論 LMWH能有效改善膿毒癥內皮細胞EPCR和PAR1錶達抑製的狀態.
목적 관찰저분자간소(LMWH)대농독증대서복주동맥내피세포(VEC)단백C수체(EPCR)화단백매활화수체1(PAR1)표체적영향.방법 채용조직첩괴법배양24지Wister대서복주동맥VEC,1:3전대지제4대,분위대조조(n=6)、농독증조(LPS 1 μg/ml,n=6)、LMWH조(LPS 1 μg/ml+LMWH 5 μg/ml,n=6).분별재제1、3、5천채용류식세포술(FCM)검측VEC표면적EPCR화PAR1적표체.결과 농독증조EPCR화PAR1적표체각시간점균교대조조유명현하강(P<0.05혹P<0.01),이제5천최위명현(26.53±7.21 vs 39.26±2.62,q=6.45,P<0.01;53.21±15.10 vs 86.54±11.34,q=6.94,P<0.01).LMWH조EPCR화PAR1적표체각시간점균고우농독증조(P<0.05);여대조조비교,EPCR재제1천잉유명현강저(40.86±1.63 vs 45.41±2.82,q=3.51,P<0.05),단제3、5천접근대조조수평(41.20±3.32 vs 42.83±2.66,P>0.05;39.23±3.33 vs 39.26±2.62,P>0.05),PAR1각시간점여대조조비교차이균무통계학의의(P>0.05).결론 LMWH능유효개선농독증내피세포EPCR화PAR1표체억제적상태.
Objective To investigate the effect of low molecular weight heparin (LMWH) on the expression of endothelial protein C receptor (EPCR) and protease activated receptor 1 (PAR1) in abdominal vascular endothelial cells (VECs) of septic rats. Methods VECs were cultured by tissue-sticking method, and the purity was determined with flow cytometry (FCM). VECs were randomly divided into three groups: control group, septic group (LPS 1 μg/ml) and LMWH group (LPS 1 μg/ml+LMWH 5 μg/ml). The VECs were collected at 1st, 3rd, 5th days after stimulated. The expression of EPCR and PAR1 were assessed by FCM. Results The expression of EPCR and PAR1 of septic group decreased significantly compared with control group at each time point (P<0.05 or P<0.01), and the expression decreased most obviously on day 5 (26.53±7.21 vs 39.26±2.62,q=6.45,P<0.01;53.21±15.10 vs 86.54±11.34,q=6.94,P<0.01). In LMWH group, the levels of EPCR and PAR1 expression were higher than setpic group at each time point (P<0.05). Compared to control group, the expression of EPCR had a significantly decrease on day 1 (40.86±1.63 vs 45.41±2.82,q=3.51,P<0.05), which had no significantly different on day 3 and 5 (41.20±3.32 vs 42.83±2.66,P>0.05;39.23±3.33 vs 39.26±2.62,P>0.05), and the expression of PAR1 were not significantly decrease compared with control group at each time point (P>0.05). Conclusions LMWH could improve the inhibition status and the expression of EPCR and PAR1 on VECs in septic rats.