基础医学与临床 ›› 2008, Vol. 28 ›› Issue (4): 354-359.

• 研究论文 • 上一篇    下一篇

别嘌呤醇降低大鼠心肌非梗死区胶原重塑

肖骏 佘强 罗开良 黄开顺   

  1. 重庆医科大学第二附属医院心内科 重庆医科大学附属第二医院心内科 重庆医科大学附属第二医院心内科 重庆医科大学基础研究所
  • 收稿日期:2007-08-22 修回日期:2007-10-17 出版日期:2008-04-25 发布日期:2008-04-25
  • 通讯作者: 佘强

Allopurinol attenuates collagen remodeling in non-infarcted myocardium after myocardial infarction in rats

Jun XIAO, Qiang SHE, Kai-liang LUO, Kai-shun HUANG   

  1. 2st Affiliated Hospital, Chongqing University of Medical Science 2st Affiliated Hospital, Chongqing University of Medical Science
  • Received:2007-08-22 Revised:2007-10-17 Online:2008-04-25 Published:2008-04-25
  • Contact: Qiang SHE,

摘要: 目的 探讨黄嘌呤氧化酶抑制剂别嘌呤醇对大鼠非梗死区心肌胶原重塑的影响。方法 结扎冠脉前降支制作大鼠心肌梗死模型,随机分为假手术组(sham,n =20),心肌梗死组(MI,n =31)和别嘌呤醇组(每天50 mg/kg,n =30),每组分别于7、14、21和28d时测定心肌组织胶原含量,Ⅰ、Ⅲ型胶原容积分数(CVF)、mRNA的改变及Ⅰ/Ⅲ型胶原比值,黄嘌呤氧化酶(XO)和清除活性氧活力(n =5),28d时另检测XO蛋白表达及左心室病理改变。结果 MI组心肌胶原含量,Ⅰ、Ⅲ型CVF及mRNA升高,Ⅰ/Ⅲ型胶原比值先下降后升高,XO活力增加,清除活性氧活力降低(P <0.05或P <0.01)。别嘌呤醇组明显缓解了上述指标的变化。结论 别嘌呤醇能够降低非梗死区胶原沉积和Ⅰ/Ⅲ型胶原比值,改善心肌梗死后心肌胶原重塑。

关键词: 别嘌呤醇, 黄嘌呤氧化酶, 活性氧, 胶原重塑, 心肌梗死

Abstract: Objective To explore the effect of xanthine oxidase inhibitors allopurinol on collagen remodeling in non-infarcted myocardium after myocardial infarction in rats.Methods Myocardial infarction models were produced by ligation of anterior descending coronary artery.The survivals were randomly divided into 3 groups:sham operation group, MI group and allopurinol group(50 mg/kg).On the 7th , 14th , 21st and 28th day respectively , the collagen content were detected.The type Ⅰ and type Ⅲ collagen volume fraction(CVF) and Ⅰ/Ⅲ ratio in non-infarcted zones(NIZ) were examined with PSR staining and the mRNA expressions were detected with RT-PCR, the activities of xanthine oxidase(XO) and O2.-,.OH-scavenging in NIZ were examined by colorimetry.In addition, the expression of XO protein by Western blotting analysis and pathological change in LV were detected on the 28th day.Results Compared with sham group,the mRNA expressions, CVF of typeⅠand type Ⅲ collagen in NIZ were increased in MI group.The typeⅠ/Ⅲ ratio in NIZ was increased after decreased.The collagen content and activity of XO were boosted but the activities of O2.-, .OH-scavenging were decreased(P <0.05 or P <0.01).Compared with MI group, the changes of these parameters above were alleviated in allopurinol group.There were no significant difference in infarct size and XO expression between allopurinol and MI group.Conclusion Allopurinol could attenuate the myocardial collagen deposition and typeⅠ/Ⅲ ratio in NIZ to improve myocardial collagen remodeling in rats after MI.

Key words: allopurinol, xanthine oxidase, reactive oxygen species, collagen remodeling, myocardial infarction