{"title":"染料木素防治大鼠关节移植动脉硬化的实验研究","authors":"Chen Bi-cheng","doi":"10.1097/00007890-200607152-02451","DOIUrl":null,"url":null,"abstract":"[Objective] To study the protective effects of genistein(GEN) in preventing and treating transplant arteriosclerosis and potential mechanisms. [Methods] Arotic transplantation was performed with male Brown-Norway rats as donors and male Lewis rats as recipients. The recipients in the experiment was randomly divided into four groups: (1) high-dose group (n=8), the recipients were administered with GEN at a dose of 20 mg/kg body weight for 60 days continuously; (2) high-low dose group (n=8), at a dose of 20 mg/kg for 14 days and at dose of 2 mg/kg for 46 days continuously; (3) solvent control (n=5), 0.5 mL DMSO for 60 days; (4) control (n=5), no treatment. Histological changes were monitored 60 days after transplantation, and the average depth of intima was calculated with computer imaging analysis systes. Immunohistochemistry was used to detect infiltration of CD4+, CD8+ T lymphocyte in the transplanted vessels, and ELISA to detect the change of VEGF in different group. [Results] Compared with two control groups, there were less lymphocytes and macrophages infiltration, the average depth of intima in two experimental groups markedly lowed (seperatedly P 0.001) and infiltration of CD4+, CD8+ T lymphocyte in the transplanted vessels was less (seperatedly P 0.01). Expression of VEGF in high dose group was lower than that in two control (8.6731±1.0466 Vs 21.8340±0.7558 and 23.2068±1.2028 P 0.01), but there was no statistic difference compared with high-low dose group. [Conclusion] Genistein can prevent the development of graft arteriosclerosis and the lowed infiltration of lymphocytes and the influenced expression of growth factors may be involved in the mechanisms.","PeriodicalId":10076,"journal":{"name":"中国现代医学杂志","volume":"1 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2006-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1097/00007890-200607152-02451","citationCount":"0","resultStr":"{\"title\":\"Experimental study of genistein in preventing and treating transplant arteriosclerosis in arotic transplantation of rat\",\"authors\":\"Chen Bi-cheng\",\"doi\":\"10.1097/00007890-200607152-02451\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"[Objective] To study the protective effects of genistein(GEN) in preventing and treating transplant arteriosclerosis and potential mechanisms. [Methods] Arotic transplantation was performed with male Brown-Norway rats as donors and male Lewis rats as recipients. The recipients in the experiment was randomly divided into four groups: (1) high-dose group (n=8), the recipients were administered with GEN at a dose of 20 mg/kg body weight for 60 days continuously; (2) high-low dose group (n=8), at a dose of 20 mg/kg for 14 days and at dose of 2 mg/kg for 46 days continuously; (3) solvent control (n=5), 0.5 mL DMSO for 60 days; (4) control (n=5), no treatment. Histological changes were monitored 60 days after transplantation, and the average depth of intima was calculated with computer imaging analysis systes. Immunohistochemistry was used to detect infiltration of CD4+, CD8+ T lymphocyte in the transplanted vessels, and ELISA to detect the change of VEGF in different group. [Results] Compared with two control groups, there were less lymphocytes and macrophages infiltration, the average depth of intima in two experimental groups markedly lowed (seperatedly P 0.001) and infiltration of CD4+, CD8+ T lymphocyte in the transplanted vessels was less (seperatedly P 0.01). Expression of VEGF in high dose group was lower than that in two control (8.6731±1.0466 Vs 21.8340±0.7558 and 23.2068±1.2028 P 0.01), but there was no statistic difference compared with high-low dose group. [Conclusion] Genistein can prevent the development of graft arteriosclerosis and the lowed infiltration of lymphocytes and the influenced expression of growth factors may be involved in the mechanisms.\",\"PeriodicalId\":10076,\"journal\":{\"name\":\"中国现代医学杂志\",\"volume\":\"1 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2006-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1097/00007890-200607152-02451\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"中国现代医学杂志\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1097/00007890-200607152-02451\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"中国现代医学杂志","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1097/00007890-200607152-02451","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
[目的]研究染料木素(genstein, GEN)防治移植动脉硬化的保护作用及其可能机制。[方法]以雄性布朗-挪威大鼠为供体,雄性刘易斯大鼠为受体进行骨移植。实验对象随机分为4组:(1)高剂量组(n=8),以20 mg/kg体重的剂量给药,连续60 d;(2)高低剂量组(n=8), 20 mg/kg剂量组,连续14天,2 mg/kg剂量组,连续46天;(3)溶剂对照(n=5), 0.5 mL DMSO, 60天;(4)对照组(n=5),不处理。观察移植后60天的组织学变化,利用计算机成像分析系统计算内膜的平均深度。采用免疫组化法检测移植血管内CD4+、CD8+ T淋巴细胞浸润情况,ELISA法检测各组血管内皮生长因子的变化。[结果]与对照组相比,两实验组移植血管中淋巴细胞和巨噬细胞浸润减少,内膜平均深度明显降低(P分别为0.001),CD4+、CD8+ T淋巴细胞浸润减少(P分别为0.01)。高剂量组VEGF表达低于对照组(8.6731±1.0466 Vs 21.8340±0.7558和23.2068±1.2028 P 0.01),但与高、低剂量组比较差异无统计学意义。[结论]染料木素可预防移植物动脉硬化的发生,降低淋巴细胞的浸润,影响生长因子的表达可能与其机制有关。
Experimental study of genistein in preventing and treating transplant arteriosclerosis in arotic transplantation of rat
[Objective] To study the protective effects of genistein(GEN) in preventing and treating transplant arteriosclerosis and potential mechanisms. [Methods] Arotic transplantation was performed with male Brown-Norway rats as donors and male Lewis rats as recipients. The recipients in the experiment was randomly divided into four groups: (1) high-dose group (n=8), the recipients were administered with GEN at a dose of 20 mg/kg body weight for 60 days continuously; (2) high-low dose group (n=8), at a dose of 20 mg/kg for 14 days and at dose of 2 mg/kg for 46 days continuously; (3) solvent control (n=5), 0.5 mL DMSO for 60 days; (4) control (n=5), no treatment. Histological changes were monitored 60 days after transplantation, and the average depth of intima was calculated with computer imaging analysis systes. Immunohistochemistry was used to detect infiltration of CD4+, CD8+ T lymphocyte in the transplanted vessels, and ELISA to detect the change of VEGF in different group. [Results] Compared with two control groups, there were less lymphocytes and macrophages infiltration, the average depth of intima in two experimental groups markedly lowed (seperatedly P 0.001) and infiltration of CD4+, CD8+ T lymphocyte in the transplanted vessels was less (seperatedly P 0.01). Expression of VEGF in high dose group was lower than that in two control (8.6731±1.0466 Vs 21.8340±0.7558 and 23.2068±1.2028 P 0.01), but there was no statistic difference compared with high-low dose group. [Conclusion] Genistein can prevent the development of graft arteriosclerosis and the lowed infiltration of lymphocytes and the influenced expression of growth factors may be involved in the mechanisms.