...
首页> 外文期刊>Asian Journal of Pharmaceutical and Clinical Research >COMBINATION EFFECT OF LISINOPRIL AND DILTIAZEM AS ANTI FIBROSIS IN PERITONEUM OF RATS
【24h】

COMBINATION EFFECT OF LISINOPRIL AND DILTIAZEM AS ANTI FIBROSIS IN PERITONEUM OF RATS

机译:利诺普利和地噻嗪对大鼠腹膜抗纤维化的联合作用。

获取原文

摘要

Objective: The objective of this research was to evaluate the effect of combination between lisinopril and diltiazem in reducing expression of transforming growth factor-β (TGF-β) and fibrosis peritoneum in a male rat treated with continuous ambulatory peritoneal dialysis (CAPD). Method : This was an experimental study, post-test only control group design. Thirsty Dawley Sprague rats are divided into five groups: Control group (Group 1), CAPD liquid 4,25% (Group 2), lisinopril 1.44 mg oral and CAPD (Group 3), and diltiazem CD 6.48 mg oral and CAPD (Group 4), lisinopril 1.44 mg+diltiazem CD 6.48 mg oral and CAPD (Group 5). After 4 weeks, rats sacrificed expression of TGF-β and peritoneal fibrosis are conducted by histopathology with hematoxylin-eosin staining and immunology with anti-human-TGF-β. Result : Twenty peritoneal of rats can be examined. Mean score of TGF-β in control group is 1, 8, in CAPD group is 2, in lisinopril and CAPD group is 1, 8, in diltiazem CD and CAPD group is 1, 8, in lisinopril and diltiazem CD and CAPD group is 1, 7 (p=0.959). Mean score of peritoneal fibrosis in control group is 1, 1, in CAPD group is 2, 6, in lisinopril and CAPD group is 1, 2, in diltiazem CD and CAPD group is 1, 3, in lisinopril and diltiazem CD, and CAPD group is 1, 5 (p=0,268). Conclusion: Combination of lisinopril and diltiazem lower the expression of TGF-β and peritoneum fibrosis better than lisinopril or diltiazem but statistically not significant. Combination of lisinopril and diltiazem lower the peritoneal fibrosis but statistically not significant, and it does not better than lisinopril or diltiazem.
机译:目的:本研究的目的是评估赖诺普利和地尔硫卓联用对连续性非卧床腹膜透析(CAPD)治疗的雄性大鼠减少转化生长因子-β(TGF-β)和腹膜纤维化的表达的作用。方法:这是一项实验性研究,仅用于对照组的后期测试。口渴的Dawley Sprague大鼠分为五组:对照组(第1组),CAPD液体4.25%(第2组),赖诺普利1.44 mg口服和CAPD(第3组)以及地尔硫卓CD 6.48 mg口服和CAPD(第4组) ),赖诺普利1.44 mg +地尔硫卓CD 6.48 mg口服和CAPD(第5组)。 4周后,通过苏木精-曙红染色的组织病理学和抗人TGF-β的免疫学进行大鼠处死TGF-β的表达和腹膜纤维化。结果:可以检查20只大鼠的腹膜。对照组中TGF-β的平均得分为1,8,CAPD组为2,赖诺普利和CAPD组为1,8,地尔硫卓CD和CAPD组为1,8,赖诺普利和地尔硫卓CD,CAPD组为1,7(p = 0.959)。对照组腹膜纤维化的平均评分为1、1,CAPS组为2、6,赖诺普利,CAPD组为1、2,地尔硫卓CD和CAPD组为1、3,赖诺普利和地尔硫卓CD,CAPD组是1、5(p = 0,268)。结论:赖诺普利和地尔硫卓联用比赖诺普利或地尔硫卓降低了TGF-β的表达和腹膜纤维化,但在统计学上无统计学意义。赖诺普利和地尔硫卓的组合可降低腹膜纤维化,但统计学上不显着,并且不比赖诺普利或地尔硫卓好。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号