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人体静脉搭桥移植物中的再狭窄

Restenosis in human vein bypass grafts.

作者信息

Nikol S, Huehns T Y, Weir L, Wight T N, Höfling B

机构信息

Department of Medicine, Klinikum Grosshadern, Ludwig Maximilians University, Munich, Germany.

出版信息

Atherosclerosis. 1998 Jul;139(1):31-9. doi: 10.1016/s0021-9150(98)00050-1.

DOI:10.1016/s0021-9150(98)00050-1
PMID:9699889
Abstract

The restenosis rate in vein bypass grafts is higher than in native coronary arteries, and both the cascade of regulatory factors and the vessel reaction may be altered. In this study, vein bypass atherectomy specimens were classified as primary (n = 10) or restenotic (n = 12). Immunohistochemistry with 11 primary antibodies showed low levels of proliferation in both tissues and similar amounts of extracellular matrix components in both primary and restenotic specimens at the time points at which tissue was removed for clinical reasons. Inflammation appeared increased in restenotic specimens. Using in situ hybridization, transforming growth factor-beta1 messenger RNA was detected in both primary and restenotic tissue, with a trend to higher expression in restenosis (8.4 +/- 5.3 vs. 9.4 +/- 7.4 grains/nucleus) and further increased expression in multiple compared with single restenoses (15.1 +/- 6.1 vs. 5.6 +/- 5.1 grains/nucleus, P < 0.05). Hence, there were no great differences in cell proliferation or extracellular matrix formation between primary and restenosis vein graft tissue, in contrast to previously described findings in arterial tissue. This suggests that primary vein graft tissue is already in a chronic 'restenosis-like' state and subsequent injury creates minimal additional upregulation.

摘要

静脉搭桥移植物的再狭窄率高于天然冠状动脉,并且调节因子级联反应和血管反应可能都会发生改变。在本研究中,静脉搭桥斑块旋切术标本被分为原发性(n = 10)或再狭窄性(n = 12)。使用11种一抗进行免疫组织化学检测显示,在因临床原因取出组织的时间点,两种组织中的增殖水平均较低,原发性和再狭窄性标本中的细胞外基质成分含量相似。再狭窄性标本中的炎症似乎有所增加。使用原位杂交技术,在原发性和再狭窄性组织中均检测到转化生长因子-β1信使核糖核酸,再狭窄中的表达有升高趋势(8.4±5.3对9.4±7.4颗粒/细胞核),与单个再狭窄相比,多个再狭窄中的表达进一步增加(15.1±6.1对5.6±5.1颗粒/细胞核,P<0.05)。因此,与先前在动脉组织中描述的结果相反,原发性和再狭窄性静脉移植物组织在细胞增殖或细胞外基质形成方面没有很大差异。这表明原发性静脉移植物组织已经处于慢性“再狭窄样”状态,随后的损伤只会产生最小程度的额外上调。

相似文献

1
Restenosis in human vein bypass grafts.人体静脉搭桥移植物中的再狭窄
Atherosclerosis. 1998 Jul;139(1):31-9. doi: 10.1016/s0021-9150(98)00050-1.
2
Expression of transforming growth factor-beta 1 is increased in human vascular restenosis lesions.转化生长因子-β1在人类血管再狭窄病变中的表达增加。
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Differential histopathology of primary atherosclerotic and restenotic lesions in coronary arteries and saphenous vein bypass grafts: analysis of tissue obtained from 73 patients by directional atherectomy.冠状动脉和大隐静脉旁路移植术中原发性动脉粥样硬化病变与再狭窄病变的组织病理学差异:对73例患者经定向旋切术获取的组织进行分析。
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Transforming growth factor-beta1 antisense treatment of rat vein grafts reduces the accumulation of collagen and increases the accumulation of h-caldesmon.转化生长因子-β1反义疗法对大鼠静脉移植物的处理可减少胶原蛋白的积累并增加h-钙调蛋白的积累。
J Vasc Surg. 2006 May;43(5):1028-36. doi: 10.1016/j.jvs.2006.01.016.
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Restenosis after directional coronary atherectomy: differences between primary atheromatous and restenosis lesions and influence of subintimal tissue resection.
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Antisense to transforming growth factor-beta1 messenger RNA reduces vein graft intimal hyperplasia and monocyte chemotactic protein 1.转化生长因子-β1信使核糖核酸的反义核酸可减少静脉移植物内膜增生和单核细胞趋化蛋白1。
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Vein adaptation to arterialization in an experimental model.在一个实验模型中静脉对动脉化的适应。
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Intracoronary beta-brachytherapy using a rhenium-188 filled balloon catheter in restenotic lesions of native coronary arteries and venous bypass grafts.使用填充铼-188的球囊导管对天然冠状动脉和静脉搭桥移植物的再狭窄病变进行冠状动脉内近距离放射治疗。
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Replication in restenotic atherectomy tissue.再狭窄斑块切除组织中的复制。
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[Expression of early growth response gene-1 and its correlative genes in autogenous vein graft and significance thereof: an experiment with rats].[早期生长反应基因-1及其相关基因在自体静脉移植中的表达及其意义:大鼠实验]
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