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血管紧张素转换酶抑制剂与血管紧张素Ⅱ受体拮抗剂对动脉内膜损伤后增生的影响

王晔玲1,赵利华1,张京平2,暴淑英3   

  1. 1. 吉林大学第一医院心内科,吉林 长春130021;2. 吉林大学第一医院药剂科,吉林 长春130021;3. 吉林省榆树市人民医院内科,吉林 榆树130025
  • 收稿日期:2003-09-05 修回日期:1900-01-01 出版日期:2004-09-28 发布日期:2004-09-28

Effects of angiotensin converting enzyme inhibitor and angiotensin Ⅱ antagonist receptor on neointima hyperplasia after vascular balloon injury

WANG Ye-ling1 ,ZHAO Li-hua1,ZHANG Jing-ping2,BAO Shu-ying3   

  1. 1.Department of Cardiology, First Hospital,Jilin University,Changchun 130021, China;2. Department of Medication, First Hospital ,Jilin University,Changchun 130021,China;3.The People′s Hospital of Yushu City, Jilin Province,Yushu 130025,China
  • Received:2003-09-05 Revised:1900-01-01 Online:2004-09-28 Published:2004-09-28

摘要: 目的:观察血管紧张素转换酶抑制剂(ACEI)captopril与血管紧张素Ⅱ(AngⅡ)的AT1受体拮抗剂valsartan对损伤动脉内膜增生的影响。 方法:以兔右颈总动脉内膜剥脱为实验模型,随机分为单纯损伤组、captopril组及valsartan组。captopril组及valsartan组术前1 d至术后14 d分别给予captopril 2 mg•kg-1•d-1与valsarta 10 mg•kg-1•d-1,单纯损伤组不给药。检测各组术前及术后7、14 d血浆组织纤溶酶原激活物(t-PA)、纤溶酶原激活剂抑制物-1(PAI-1)、血浆内皮素(ET)水平,并于术后14 d对各组血管内膜厚度及管腔狭窄度行病理形态学观察。 结果:captopril组及valsartan组血浆PAI-1、ET水平及内膜的厚度、管腔狭窄度均明显低于单纯损伤组(P<0.05)。 结论:captopril与valsartan均可抑制动脉损伤后内膜的增生。

关键词: 血管紧张素Ⅱ, 拮抗剂和抑制剂, 血管内膜, 损伤, 增生

Abstract: Objective To study the effects of angiotensin converting enzyme inhibitor(captopril) and angiotensin Ⅱ antagonist receptor (valsartan) on neointima hyperplasia after vascular balloon injury. Methods Thirty-six rabbit models were randomly divided into three groups:injuried group,captopril group and valsartan group. Captopril (2 mg•kg-1•d-1 po) and valsartan (10 mg•kg-1•d-1 po) were given to twelve rabbits respectively from 1 day before the right carotid arteries were injuried by 2.0 mm ballon cathether to 14 days after injury in captopil group and valsartan group. The medicine was not administered in the injuried group. The tissue plasminogen activator (tPA),plaminogen activor inhibitor-1(PAI-1) antigen level and plasma endothelin (ET) levels were measured before injury, and 7,14 days after vascular injury. The pathomorphoiogical examination were carried out 14 days after angioplasty. Results The levels of plasma PAI-1 and ET in captopril group and valsartan group were significantly lower than those in the injuried group(P<0.05).The intimal thickness and extent of lumen stenosis in captopril and valsartan groups were significantly lower than those in the injuried group (P<0.05). Conclusion Captopril and valsartan can inhibit neointima hyperplasia after vascular ballon injury.

Key words: angiotensin Ⅱ, antagonists and inhibitors, vessel intimal, injury, hyperplasi

中图分类号: 

  • R972