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新生内膜上富含纤维蛋白和血小板的血栓形成:重组组织因子途径抑制剂可预防兔主动脉反复球囊损伤后纤维蛋白形成和新生内膜发育。

Fibrin-rich and platelet-rich thrombus formation on neointima: recombinant tissue factor pathway inhibitor prevents fibrin formation and neointimal development following repeated balloon injury of rabbit aorta.

作者信息

Asada Y, Hara S, Tsuneyoshi A, Hatakeyama K, Kisanuki A, Marutsuka K, Sato Y, Kamikubo Y, Sumiyoshi A

机构信息

First Department of Pathology, Miyazaki Medical College, Japan.

出版信息

Thromb Haemost. 1998 Sep;80(3):506-11.

PMID:9759635
Abstract

Thrombus formation and neointimal growth are the critical events in restenosis after balloon angioplasty. However, the responses of diseased vessels to injuries caused by balloon angioplasty have not been well examined. We investigated the thrombus formation and neointimal development following the balloon injury to the previously induced neointima in the rabbit aorta and the effects of recombinant tissue factor pathway inhibitor (rTFPI) on these responses. Rabbit thoracic aortas were subjected to injury with a Fogarty 4F balloon catheter at 1.75 atm (first injury), and 4 weeks later the same vessels were subjected to the second injury with a Swan-Ganz 5F balloon catheter at 1.4 atm (mild-injury group) or 1.8 atm (severe-injury group), and immediately after that a retrograde bolus injection of rTFPI (100 microg/kg body weight) or saline was performed into the injured segments via the central tube of the Swan-Ganz catheter. Twenty minutes after the second injury, the injured surfaces were covered with platelet-rich thrombi in the mild-injury group and with fibrin-rich thrombi in the severe-injury group. Damaged intimal smooth muscle cells, which were immunohistochemically positive for tissue factor (TF), were observed beneath the fibrin-rich thrombi. The neointima 4 weeks after the second injury was significantly thicker in the severe-injury group than in the mild-injury group. The bolus infusion of rTFPI markedly inhibited fibrin formation on the injured surfaces, and significantly reduced the neointimal development in the severe-injury group at 4 weeks after the second injury. These results indicate that TF-dependent coagulation pathway is primarily responsible for fibrin-rich thrombus formation and may play an important role in neointimal development following the balloon injury to the rabbit aortic neointima. Additionally the bolus administration of rTFPI to the injured vessels could prevent mural thrombus formation and neointimal growth after balloon angioplasty.

摘要

血栓形成和新生内膜生长是球囊血管成形术后再狭窄的关键事件。然而,病变血管对球囊血管成形术所致损伤的反应尚未得到充分研究。我们研究了兔主动脉先前诱导的新生内膜受到球囊损伤后的血栓形成和新生内膜发展,以及重组组织因子途径抑制剂(rTFPI)对这些反应的影响。兔胸主动脉用Fogarty 4F球囊导管在1.75个大气压下进行损伤(首次损伤),4周后,同一血管用Swan-Ganz 5F球囊导管在1.4个大气压(轻度损伤组)或1.8个大气压(重度损伤组)进行第二次损伤,随后立即通过Swan-Ganz导管的中心管向损伤节段逆行推注rTFPI(100μg/kg体重)或生理盐水。第二次损伤后20分钟,轻度损伤组的损伤表面覆盖有富含血小板的血栓,重度损伤组的损伤表面覆盖有富含纤维蛋白的血栓。在富含纤维蛋白的血栓下方观察到免疫组织化学检测组织因子(TF)呈阳性的受损内膜平滑肌细胞。第二次损伤后4周,重度损伤组的新生内膜明显比轻度损伤组厚。推注rTFPI显著抑制了损伤表面的纤维蛋白形成,并显著减少了第二次损伤后4周重度损伤组的新生内膜发展。这些结果表明,TF依赖的凝血途径主要负责富含纤维蛋白的血栓形成,并且可能在兔主动脉新生内膜受到球囊损伤后的新生内膜发展中起重要作用。此外,向受损血管推注rTFPI可以预防球囊血管成形术后壁血栓形成和新生内膜生长。

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