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作 者:李兆艾[1] 智明春[1] 乔翠峰[1] 孙静汾[1]
出 处:《中华妇幼临床医学杂志(电子版)》2006年第2期78-80,共3页Chinese Journal of Obstetrics & Gynecology and Pediatrics(Electronic Edition)
基 金:山西省卫生厅资助项目(200417)
摘 要:目的观察人参皂苷Rg3(Rg3)对大鼠子宫内膜异位症(endometriosis,EMs)组织中血管内皮生成因子(vascular endothelial growth factors,VEGF)影响和抗血管生成作用。方法参照Jones方法建立Wistar大鼠EMs动物模型,3周后将建模成功的大鼠随机分为空白对照、孕三烯酮和Rg3各2,4,6 及8周组,共12组。用SABC免疫组化法测定异位灶组织中VEGF的表达。结果Rg3治疗大鼠EMs模型 2,4,6,8周后,异位组织中VEGF的表达明显低于对照组,差异有显著意义(P<0.05);而孕三烯酮治疗相同时间后与对照组相比,VEGF表达无明显改变,差异无显著意义(P>0.05);Rg3组随治疗时间延长, VEGF明显减少(P<0.05),而对照组和孕三烯酮组无此表现。结论 Rg3对大鼠子宫内膜异位组织中 VEGF表达和新生血管生成均有抑制作用。Rg3有望成为子宫内膜异位抗血管生成治疗新药。Objective To observe the effect of ginsenoside Rg3 on the expression of vascular endothelial growth factors(VEGF) and antiangiogenesis in ectopic endometrium of rats. Methods Wistar rats endometriosis models were established referring to Jones methods, the model rats were divided into the control group, ginsenoside Rg3 group, gestrinone group, each group were divided into 2 weeks, 4 weeks, 6 weeks and 8 weeks. VEGF was observed in ectopic endometrium by immunohistochemistry (SABC technique). Results VEGF in ectopic endometrium were decreased remarkably after treatment of ginsenoside Rg3 after 2,4,6,8 weeks (P〈0.05), while the difference was not significant (P 〈0.05) in the gestrinone group. And with the time prolonging, the expression of VEGF was reduced remarkably(P 〈0.05) while the change was not observed in the control group and the gestrinone group. Conclusion Ginsenoside Rg3 has the effect on inhibiting the expression of VEGF and angiogenesis in ectopic endometrium of rats. Ginsenoside Rg3 maybe a new drug of antiangiogenesis in ectopic endometrium.
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