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构建重组组织纤溶酶原激活物基因质粒预防换机械瓣术后血栓 被引量:2

Experimental study on construction of recombinant t-PA gene plasmid to prevent the thrombosis after mechanical valve replacement
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摘要 目的探讨构建的组织纤溶酶原激活物(tissueplaminogenactivator,t-PA)基因质粒对预防机械瓣膜置换术后血栓形成的作用。方法人工构建t-PA基因表达质粒,用阳离子质脂体包裹并制备成基因缝线。选择18只猪随机分为实验组和对照组,每组9只,行三尖瓣膜置换术的同时将基因缝线缝合于心肌组织,以超声波辅助转导心脏细胞产生高活性t-PA,观察术后瓣膜血栓形成、凝血功能和纤溶降解产物D-二聚体含量以及动物生存状况。结果成功构建了t-PA基因质粒并获得在心脏中表达。在对照组,于术后第1周血D-二聚体含量达高峰,平均(1.7±0.8)mg/L,于第2周明显下降接近术前;实验组于术后1周明显增高达(1.8±0.8)mg/L,与对照组差异无统计学意义(P>0.05);此后观察各期仍维持较高状态,术后2,4,8和12周检测值分别为(1.3±0.5)mg/L、(1.2±1.0)mg/L、(1.8±1.2)mg/L和(1.9±0.8)mg/L,比对照组均显著增高(P<0.01)。对照组瓣口和瓣周血栓形成率9/9,而实验组仅1/9(P<0.01)。结论构建的t-PA基因质粒可预防机械瓣膜置换术后血栓形成。 Objectives To study on a constructed tissue plaminogen activator (t-PA) to prevent the thrombosis after mechanical valve replacement. Methods A t-PA gene plasmid was constructed and packaged with a novel cationic phosphonolipid and a t-PA gene thread was made. 18 pigs were selected and subgrouped into two groups: 9 in experimental and 9 in control group for the mechanical tricuspid valve replacement. In experimental group, the gene threads were sutured into the wall of heart with the ultrasound treatment for the gene transfection at the same time of operation. The thrombosis on the valves, coagulative function and D-dimer level of the blood were observed. Results t-PA gene plasmid was successfully constructed and t-PA protein was expressed in the heart. D-dimer reached its peak level of (1.7±0.8)mg/L one week after operation, with no difference when compared with the experimental group, and decreased thereafter in the control group. In experimental group, D-dimer increased 1 week after operation with the content of (1.8±0.8)mg/L and kept its high level in the observed period with the contents of (1.3±0.5)mg/L, (1.2±1.0)mg/L,(1.8±1.2)mg/L and (1.9±0.8)mg/L 2,4,8 and 12 week after operation,respectively. There were thrombosis around the valves in all conuol group pigs(9/9)and only one had thrombosis in experimental group (1/9). Conclusions The construted tPA gene plasmid could be used for the prevention of thrombosis after mechanical valve replacement.
出处 《岭南心血管病杂志》 2006年第2期132-135,共4页 South China Journal of Cardiovascular Diseases
基金 深圳市科技计划项目200104048
关键词 组织纤溶酶原激活物 D-二聚体 血栓形成 机械瓣膜置换术 Tissue-type plasminogen activator D-dimer Thrombosis Mechanical valve replacement
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参考文献7

  • 1GILLINOV AM,COSGROVE DM.Current status of mitral valve repair[ J].Am Heart Hospital J,2003,1 (1):47-54.
  • 2WU ZJ,YANG SF,ZHENG SS,et al.Construction and biological activities of human tPA eukaryotic expression plasmid[J].Hepatobiliary Pancreat Dis Int,2004,3(4):511-515.
  • 3PODRAZIK RM,WHITEHILL TA,EKHTERAE D,et al.High-level expression of recombinant human tPA in cultivated canine endothelial cells under varying conditions of retroviral gene transfer[J].Ann Surg,1992,216(4):446-452.
  • 4EKHTERAE D,STANLEY JC.Retroviral vector-mediated transfer and expression of human tissue plasminigen activator gene in human endothelial and vascular smooth muscle cells[J].J Vasc Surg,1995,21(6):953-962.
  • 5ALBERS GW,AMARENCO P,EASTON JD,et al.Antithrombotic and thrombolytic therapy for ischemic stroke:the Seventh ACCP Conference on Antithrombotic and Thrombolytic Therapy,[J].Chest,2004,126(3 Suppl):483S-512S
  • 6郑卫,霍勇,邢德智,陈光慧,高炜,朱国英,汤健,周爱儒.血管内皮生长因子基因治疗犬闭塞性血管病的初步研究[J].中华心血管病杂志,1998,26(1):62-64. 被引量:17
  • 7PORTER TR,XIE F.Therapeutic ultrasound for gene delivery[ J ].Echocardiography,2001,18(4):349-353.

二级参考文献1

  • 1周爱儒,中华医学杂志,1996年,769卷,662页

共引文献16

同被引文献13

  • 1吴忠均,杨素芬,郑树森,时德,李德卫,骆旭东.联合转染血管内皮生长因子165和组织纤溶酶原激活物基因抑制兔血管损伤后内膜增生的研究[J].中华外科杂志,2005,43(13):861-865. 被引量:7
  • 2季军,张浩伟,张宗久,令文萍.转染组织型纤溶酶原激活物基因质粒预防狗冠脉搭桥术吻合口再狭窄[J].中国现代医学杂志,2007,17(14):1683-1686. 被引量:6
  • 3Chikwe J,Chiang YP,Egorova NN,et al. Survival and outcomes following bioprosthetic vs mechanical mitral valve replacement in patients aged 50 to 69 years[J].JAMA,2015,313(14):lg35-1442.
  • 4Johnston DR,Soltesz EG,Vakil N,et al.Long-term durability of biopros- thetic aortic valves: implications from 12 569 implants [J].Ann Thorac Surg,2015,99(4): 1239-1247.
  • 5Songur CM,Simsek E,Ozen A,et al.Long term results comparing mechani- cal and biological prostheses in the tricuspid valve position: which val- vetypes are better--mechanical or biological prostheses [J].Heart Lung Circ,2014,23(12):1175-1178.
  • 6Saleeb SF,Newburger JW,Geva T,et al.Accelerated degeneration of a bovine pericardial bioprosthetic aortic valve in children and young adults [J]. Circulation,2014,130(1 ):51-60.
  • 7Joshi V,Prosser K,Richens D.Early prosthetic valve degeneration with Mitroflow aortic valves:determination of incidence and risk factors[J].In- teract Cardiovasc Thorac Surg,201g,19(1):36-g0.
  • 8Thourani VI-I,Gunter RL,Hurst S,et al.Postoperative warfarin following mitral valve repair or bioprosthetic valve replacement[J].Heart Valve Dis, 2013,22(5):716-723.
  • 9Fugate JE,Rabinstein AA.Update on intravenous recombinant tissue plasminogen activator for acute ischemic stroke{J].Mayo Clin Proe,2014,89 (7):960-972.
  • 10Ji J,Ji SY,Yang JA,et al.Uhrasound-targeted transfection of tissue-type plasminogen activator gene carried by albumin nanoparticles to dog my- ocardium to prevent thrombosis after heart mechanical valve replacement [J].Int Journal of Nanomedicine,2012,7(1):2911-2919.

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