期刊文献+

阿托伐他汀对移植动脉硬化抑制作用的实验研究 被引量:1

Depressant effect of atorvastatin on arteriosclerosis of aortic allograft in rats
下载PDF
导出
摘要 目的研究阿托伐他汀(atorvastatin)对大鼠移植动脉硬化的抑制作用。方法建立大鼠腹主动脉移植模型。动物分为3组:(1)异系移植对照组;(2)异系移植实验组;(3)同系移植对照组。6 0 d后对移植动脉行病理组织学检测,观察移植动脉内膜增生程度,并行免疫组织化学染色(SP法)检测移植动脉增殖细胞核抗原(PCNA)和平滑肌肌动蛋白(α-SMA)的表达情况。结果异系移植实验组血管内膜增厚程度显著低于异系移植对照组,(1),(2),(3)组移植动脉内膜增厚面积比分别为(3 5.2 0±6.3 5)%,(1 2.4 0±2.6 5)%,(1.2±1.1 0)%,差异均有统计学意义(P<0.05)。PCNA在异系移植实验组表达明显低于异系移植对照组和高于同系移植对照组,(1),(2),(3)组分别为(1 7.2 0±1.6 5)%,(5.4 0±0.8 0)%,(1.1 0±0.2 5)%,差异有统计学意义(P<0.05)。结论阿托伐他汀可抑制大鼠移植动脉硬化,PCNA基因表达的下调可能是阿托伐他汀抑制移植动脉硬化的机制之一。 Objective To study the depressant effect of atorvastatin on arteriosclerosis of aortic allograft in rats. Methods The models of abdominal aorta transplantation were established in rats with the use of micro-surgery. The recipients were divided into three groups: allograft control group, allograft experimental group and isograft control group. After 60 days of transplant, vascular intimal thickness ( VIT ) in all of the groups was observed by histological examination. The expression of PCNA and α-SMA was determined by immunohistochemistry. Results The degree of VIT in rats of the allograft experimental group was lower than thai in the allograft control group; the VIT area ratio in the allograft control group, allograft experimental group and isograft control group was (12.40±2.65)% , (5.20 ±6.35)% , and (1.2 ±1. 10)% , respectively, A statistical difference between these groups was observed ( P 〈 0. 05 ) . The expression level of PCNA was lower in allograft experimental group ( 5. 40 ±0. 80 ) % than that in allograft control group ( 17.20 ±1.65 ) % ( P 〈 0.05 ) . Conclusions The expression of PCNA in the transplant aorta and the arteriosclerosis of aortic allograft could be suppressed by atorvastatin.
出处 《中国普通外科杂志》 CAS CSCD 2006年第5期345-348,共4页 China Journal of General Surgery
基金 国家自然科学基金资助项目(30271242)
关键词 动脉/移植 阿托伐他汀/治疗应用 基因表达 模型 动物 Arteris/transpl Atorvastatin/ther use Gene Expression Models, Animal
  • 相关文献

参考文献9

  • 1李幼平.移植免疫生物学[M].北京:科学出版社,2000.106.
  • 2Van Leuven SI, Kastelein JJ. Atorvastatin. Expert Opin Pharmacother [J]. 2005,6(7):1191 - 1203.
  • 3Lea AP, Mc Tavish D. Atorvastatin A review of its pharmacology and therapeutic potential in the management of hyperlipidaemias [J]. Drags, 1997,53(5):828 -847.
  • 4Xu CB, Stenman E, Edvinsson L, et al. Reduction of bFGF-induced smooth muscle cell proliferation and endothelin receptor mRNA expression by mevastatin and atorvastatin. Biochem Pharmacol [J]. 2002,64(3):497-505.
  • 5Ludwig A, Friedel B, Metzkow S, et al. Effect of statins on the proteasomal activity in mammalian endothelial and vascular smooth muscle cells[ J ] . Biochem Pharmacol, 2005 , 70 ( 4 ) :520 - 526.
  • 6Blanco-Colio LM, Villa A, Ortego M, et al. 3-Hydroxy-3-methyl-glutaryl coenzyme A reductase inhibitors, atorvastatin and simvastatin, induce apoptosis of vascular smooth muscle cells by downregulation of Bcl-2 expression and Rho A prenylation [ J ] .Atherosclerosis, 2002 , 161 ( 1 ) : 17 - 26.
  • 7Bubonva MG. Atorvastatin : lipid lowering activity, pleiotropic properties and efficacy in prevention of atherosclerosis and coronary heart disease [ J ] . Kardiologiia, 2004 , 44(8): 96 - 104.
  • 8Hulhaupt F, Matter CM, Kwak BR, et al. Statins ( HMG-CoA reductase inhibitors ) reduce CD40 expression in human vascular cells [J]. Cardiovasc Res, 2003,59(3) :755 -766.
  • 9Haloui M, Meilhac 0, Jandrot-Pererus M, et al. Atorvastatin limits the pro-inflammatory response of rat aortic smooth muscle cells to thrombin [J]. Eur J Pharmacol, 2003,474(2-3):175 - 184.

共引文献5

同被引文献5

  • 1石铮,王家兴,何庆良,曾金华.人RhoC基因正、反义真核表达载体的构建及对肿瘤增殖的影响[J].中华实验外科杂志,2005,22(11):1289-1291. 被引量:7
  • 2Olnes JM, Erlich R. A review and update to cholangiocarcinoma[ J ] . Oncology,2004,66 (6) : 167 - 179.
  • 3Calabro P, Yeh TH. The pleiotropic effects of statins [ J ]. Curr Opin Cardiol, 2005,20 ( 6 ) : 541 - 546.
  • 4Fero ML, Rivkin M, Tasch M, et al. A syndrome of multiorgan hyperplasia with features of gigantism, tumdrigenesis, and female sterility in p27 ( Kip )- deficient mice [ J ]. Cell, 1996,85(5) :733 -744.
  • 5Jamagin WR, Klimstra DS, Hezel M, et al. Differential cell cycle-regulatory protein expression in biliary tract adenocarcinoma : correlation with anatomic site, pathologic variables, and clinical outcome [ J ] . Journal of Clinical Oncology, 2006,24 (7) :1152-1160.

引证文献1

二级引证文献1

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部