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基质金属蛋白酶及其抑制剂在家兔血管成形术后血管重构中的作用 被引量:7

Role of MMP2/TIMP1 in the vascular remodeling after angioplasty in rabbits
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摘要 目的:探讨基质金属蛋白酶及其抑制剂(MMPs/TIMPs)在家兔血管成形术后血管重构中的作用及中药通心络的影响。方法:(1)家兔65只分4组(对照组5只,拉伤组20只,高脂组20只,通心络组20只)采用高胆固醇(1·5g·kg-1·d-1)喂养加两次腹主动脉损伤的方法制成动脉粥样硬化和血管成形术模型,X光下行血管成形术。术后分别治疗4周处死,取血管标本进行检测。(2)HE染色计算机图像分析血管形态的变化。(3)MMP2和TIMP1免疫组化分析,RT-PCR方法测定MMP2、TIMP1的mRNA表达量。结果:(1)HE染色证实有动脉粥样硬化斑块形成,腹主动脉造影显示有管腔狭窄。(2)RT-PCR结果显示通心络组的MMP2和TIMP1mRNA表达量低于高脂拉伤组P<0·05;MMP2和TIMP1比值更接近1。(3)免疫组化染色通心络组MMP2和TIMP1的阳性细胞吸光度(%)明显低于高脂拉伤组,P<0·05。(4)内膜面积通心络组低于高脂拉伤组P<0·05;而管腔面积高于高脂拉伤组P<0·05;并且管腔面积的增加与内膜面积的减少不相等。结论:MMP2和TIMP1参与家兔血管成形术后的血管重构,通心络可以调整MMP2和TIMP1的比值。 AIM: To discuss the effects of matric metalloproteinasez and tissue inhibitor 1 ( MMP2/TIMP1 ) on the vascular remodeling after angioplasty and the regulatory effect of tongxinluo on it in rabbits. METHODS: 65 nrale white rabbits (2.5- 3.5 kg; 6 - 8 months) were divided into 4 groups: control group ( n = 5, normal diet ), injury group ( n = 20, normal diet plus intimal injury), high - lipid group ( n = 20, high cholesterol diet plus intimal injury) and tongxinluo group ( n = 20, tongxinluo 0.5mg·kg^-1·d^-1, 4 weeks, also high cholesterol diet plus intimal injury). Under X - ray the narrow parts of the vessel underwent angioplasty.All rabbits were. killed and vessel samples were excised, respectively, for the detection of histomorphometry inununohistochemically and RT - PCR. The data were expressed as x ± s. RESULTS: ( 1 ) The change of vascular morphological results showed that the intimal area in tongxinluo group was less than that in high - lipid group ( P 〈 0.05), inversely the lumen area in tongxirduo group was higher than that in high - lipid group ( P 〈 0.05). The difference between the increase in lumen area and the decrease in intimal area suggested that the vascular remodeling exist. (2) RT - PCR showed that the relative level of mRNA of MMP2 and TIMPI in tongxinluo group was less than those in high - lipid group ( P 〈 0.05). (3) The immunohistochemical staining showed that the light absorption of MMP2 and TIMPI in Tongxinluo group was less than that in high - lipid group ( P 〈 0.05).CONCLUSION: Tongxinluo inhibits the accumulation and secretion of extracellular matrix, also inhibits vascular remodeling in rabbits, which is related with MMP2 and TIMP1.
出处 《中国病理生理杂志》 CAS CSCD 北大核心 2005年第8期1503-1507,共5页 Chinese Journal of Pathophysiology
基金 辽宁省自然科学基金资助项目
关键词 基质金属蛋白酶 血管成形术 血管重塑 通心络 Matric metalloproteinases Angioplasty Vascular remodeling Tong - xin - luo
作者简介 Tel:024-23269384
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参考文献8

  • 1徐贵成,高荣林,吴以岭,刘俊玲,高学东,李辉.通心络胶囊治疗冠心病心绞痛的临床研究[J].中国中西医结合杂志,1997,17(7):414-416. 被引量:162
  • 2郗永安,汪丽蕙.血管成形术后再狭窄实验模型[J].中国介入心脏病学杂志,1995,3(4):189-191. 被引量:16
  • 3Bauters C, Isner JM. The biology of restenosis[ J]. Prog Cardiovasc Dis, 1997, 40(2): 107- 116.
  • 4Lefkovits J, Topol EJ. Pharmacological approaches for the prevention of restenosis after percutaneous coronary intervention[J]. Prog Cardiovasc Dis, 1997, 40(2): 141 - 158.
  • 5on DP, Coats W, Currier J. Remodeling of the coronary artery after vascular injury[J]. Prog Cardiovasc Dis, 1997, 40(2):129- 140.
  • 6Spinale FG, Coker ML, Bond BR, et al. Myocardial matrix degradation and matelloproteinase activation in the failing heart: a potential therapeutic target [ J]. Cardiovasc Res,2000, 46(2): 225 - 238.
  • 7Peterson TJ, Li H, Dillon L, et al. Evaluation of matrix metalloproteinase and tissue inhibitor expression during heart failure progression in the infarction rat [ J ]. Cardiovasc Res,2000, 46(2): 307 - 315.
  • 8张恩光,张怀勤,林捷,黄伟建,李上共,徐力辛.基质金属蛋白酶在心肌缺血大鼠心室间质重构中的作用[J].中国病理生理杂志,2003,19(5):653-656. 被引量:7

二级参考文献13

  • 1Dollery CM, McEwan JR, Henney AM. Matrix metalloproteinases and cardiovascular disease[J]. Circ Res, 1995,77(5) :863 - 868.
  • 2Kleiner DE, Stetler- Stevenson WG. Quantitative zymography: detection of picogram quantities of gelatinases[J].Anal Biochem, 1994, 218(2) : 325 - 332.
  • 3Chiariello M, Ambrosio G, Cappelli- Bigazzi M, et al. A biochemical method for the quantitation of myocardial scarring after experimental coronary artery occlusion[J]. J Mol Cell Cardiol, 1986,18(3) :283- 290.
  • 4Cleutjens JP, Kandala JC, Guarda E, et al. Regulation of collagen degradation in the rat myocardium after infarction[J]. J Mol Cell Cardiol, 1996, 27(6): 1281 - 1292.
  • 5Dixon IM, Ju H, Jassal DS, et al. Effect of ramipril and losartan on collagen expression in right and left heart after myocardial infarrction[J]. Mol Cell Biochem, 1996, 165(1):31-45.
  • 6Carlyle WC, Jacobson AW, Judd DL, et al. Delayed reperfusion alters matrix metalloproteinase activity and fibronectin mRNA expression in the infarct zone of the ligated rat heart[J]. J Mol Cell Cardiol, 1997, 29(9) : 2451 - 2463.
  • 7Cleutjens JP, Verluyten MJ, Smiths JF, et al. Collagen remodeling after myocardial infarction in the rat heart[J]. Am J Pathol, 1995, 147(2) : 325 - 338.
  • 8Wei S, Chow LT, Shum IO, et al. Left and right ventricuIar collagen type Ⅰ/Ⅲ ratios and remodeling post- myocardial infarction[J]. J Card Fail, 1999, 5(2) : 117 - 126.
  • 9团体著者,中药新药临床研究指导原则.第1辑,1993年,41页
  • 10陈可冀,心脑血管疾病研究,1988年,318页

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