国际中医中药杂志
國際中醫中藥雜誌
국제중의중약잡지
INTERNATIONAL JOURNAL OF TRIDITIONAL CHINESE MEDICINE
2012年
4期
324-326
,共3页
南蛇藤%血管生成%循环血管内皮细胞%血管内皮生长因子
南蛇籐%血管生成%循環血管內皮細胞%血管內皮生長因子
남사등%혈관생성%순배혈관내피세포%혈관내피생장인자
Celastrus orbiculatus%Angiogenesis%CECs%VEGF
目的 观察南蛇藤总萜对Hepal-6荷瘤小鼠外周血VEGF、CECs的影响.方法 采用常规无菌接种技术制作小鼠肝癌Hepal-6移植性肿瘤模型,观察南蛇藤总萜高、中、低剂量(40 mg/kg、20 mg/kg、10 mg/kg)对Hepal-6荷瘤小鼠外周血VEGF、CECs表达的影响.结果 南蛇藤总萜在20 mg/kg时,外周血VEGF (45.24±21.36) pg/ml、CECs (0.83±0.10)%表达明显降低,与阴性对照组(0.9%生理盐水)比较,差异有统计学意义(P<0.01).结论 南蛇藤总萜可明显降低VEGF、CECs表达,这一作用可能与南蛇藤总萜抑制肝癌血管生成有关.
目的 觀察南蛇籐總萜對Hepal-6荷瘤小鼠外週血VEGF、CECs的影響.方法 採用常規無菌接種技術製作小鼠肝癌Hepal-6移植性腫瘤模型,觀察南蛇籐總萜高、中、低劑量(40 mg/kg、20 mg/kg、10 mg/kg)對Hepal-6荷瘤小鼠外週血VEGF、CECs錶達的影響.結果 南蛇籐總萜在20 mg/kg時,外週血VEGF (45.24±21.36) pg/ml、CECs (0.83±0.10)%錶達明顯降低,與陰性對照組(0.9%生理鹽水)比較,差異有統計學意義(P<0.01).結論 南蛇籐總萜可明顯降低VEGF、CECs錶達,這一作用可能與南蛇籐總萜抑製肝癌血管生成有關.
목적 관찰남사등총첩대Hepal-6하류소서외주혈VEGF、CECs적영향.방법 채용상규무균접충기술제작소서간암Hepal-6이식성종류모형,관찰남사등총첩고、중、저제량(40 mg/kg、20 mg/kg、10 mg/kg)대Hepal-6하류소서외주혈VEGF、CECs표체적영향.결과 남사등총첩재20 mg/kg시,외주혈VEGF (45.24±21.36) pg/ml、CECs (0.83±0.10)%표체명현강저,여음성대조조(0.9%생리염수)비교,차이유통계학의의(P<0.01).결론 남사등총첩가명현강저VEGF、CECs표체,저일작용가능여남사등총첩억제간암혈관생성유관.
Objective To study the effects of Celastrus orbiculatus extracts (COE) on the expression of VEGF and CECs of Hepal-6 tumor bearing mice.Methods Animal Models of Hepal-6 portability liver tumor bearing mice were established and randomly assigned to six groups (eight mice per group) as follows:untreated control group,solvent vehicle control (DMSO) group,physiological saline control group,cisplatin-treated group,and different dosages COE-treated groups (40 mg/kg,20 mg/kg,10 mg/kg).To approach the effects of COE on the expression of VEGF and CECs in Hepal-6 toumor bearing mice.Results The ELISA and flow cytometer showed that COE could significantly inhibit the expression of VEGF(45.24±21.36) pg/ml and CECs (0.83 ± 0.10) % compared with the physiological saline control group (P< 0.01 ) with the dose of 20mg/kg.Conclusion COE could significantly down-regulate the expression of VEGF and CECs.It may be related with the effect of COE in inhibiting angiogenesis of tumor.