Anti-inflammatory effects of long-lasting locally-delivered human recombinant tissue factor pathway inhibitor after balloon angioplasty

被引:21
作者
Nakamura, Y
Nakamura, K
Ohta, K
Matsubara, H
Yutani, C
Hamuro, T
Kato, H
Ohe, T
机构
[1] Okayama Univ, Grad Sch Med & Dent, Dept Cardiovasc Med, Okayama 7008558, Japan
[2] Natl Cardiovasc Ctr, Dept Pathol, Osaka 5600873, Japan
[3] Natl Cardiovasc Ctr, Inst Res, Osaka 5600873, Japan
[4] Chemo Sero Therapeut Res Inst, Kumamoto 8691205, Japan
关键词
thrombosis; angioplasty; restenosis; arteries; inflammation;
D O I
10.1007/s003950200012
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Tissue factor pathway inhibitor (TFPI) has anti-proliferative and anti-migratory effects on cultured smooth muscle cells (SMC) in addition to its anti-thrombotic activity. Here, we assess how long locally delivered recombinant TFPI (rTFPI) remains detectable at the delivery sites and clarify the main mechanism by which rTFPI blocks neointimal growth in vivo. Methods. The iliac arteries of 85 Japanese white rabbits were injured using a Cutting Balloon(TM). First, to establish the efficacy of local delivery of rTFPI, 5 groups of 3 rabbits each were examined immediately or 1, 2, 4 or 7 days after delivery. They were treated locally with a total amount of 200 mug of rTFPI given at 40 mug per pulse per minute by means of a Pulse Spray(TM) catheter. Thereafter, 34 rabbits which had received 200 mug of rTFPI after cutting angioplasty were compared to the same number of controls regarding thrombosis, inhibition of neointimal proliferation and inflammation. Results A total of 2.6 +/- 1.6 ng rTFPI persisted on the injured vessel 4 days after delivery. rTFPI was still present on 48 % of the cut sites 7 days after delivery, despite its short half-life in plasma. Thrombosis in the rTFPI-treated group was significantly reduced compared to the controls. The number of macrophages present within the media and intima was significantly decreased at day 7 after delivery of rTFPI. Furthermore, the number of Ki-67-positive cells 14 days after rTFPI delivery was significantly lower than in controls although there were no significant differences between them after 2 days. Conclusions Local delivery of rTFPI decreased the degree of neointimal formation 4 weeks after TFPI delivery because of anti-inflammatory and anti-proliferative effects in addition to, or rather than, via anti-thrombosis.
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收藏
页码:198 / 205
页数:8
相关论文
共 21 条
[1]   AN ANTITISSUE FACTOR PATHWAY INHIBITOR (TFPI) MONOCLONAL-ANTIBODY RECOGNIZED THE 3RD KUNITZ DOMAIN (K3) OF FREE-FORM TFPI BUT NOT LIPOPROTEIN-ASSOCIATED FORMS IN PLASMA [J].
ABUMIYA, T ;
ENJYOJI, K ;
KOKAWA, T ;
KAMIKUBO, Y ;
KATO, H .
JOURNAL OF BIOCHEMISTRY, 1995, 118 (01) :178-182
[2]   IMMUNOHISTOCHEMICAL DETECTION OF KI-67 IN REPLICATIVE SMOOTH-MUSCLE CELLS OF RABBIT CAROTID ARTERIES AFTER BALLOON DENUDATION [J].
AOYAGI, M ;
YAMAMOTO, M ;
WAKIMOTO, H ;
AZUMA, H ;
HIRAKAWA, K ;
YAMAMOTO, K .
STROKE, 1995, 26 (12) :2328-2331
[3]   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 [J].
Asada, Y ;
Hara, S ;
Tsuneyoshi, A ;
Hatakeyama, K ;
Kisanuki, A ;
Marutsuka, K ;
Sato, Y ;
Kamikubo, Y ;
Sumiyoshi, A .
THROMBOSIS AND HAEMOSTASIS, 1998, 80 (03) :506-511
[4]   CUTTING BALLOON - A NOVEL-APPROACH TO PERCUTANEOUS ANGIOPLASTY [J].
BARATH, P ;
FISHBEIN, MC ;
VARI, S ;
FORRESTER, JS .
AMERICAN JOURNAL OF CARDIOLOGY, 1991, 68 (11) :1249-1252
[5]   PULSE-SPRAY PHARMACOMECHANICAL THROMBOLYSIS [J].
BOOKSTEIN, JJ ;
VALJI, K .
CARDIOVASCULAR AND INTERVENTIONAL RADIOLOGY, 1992, 15 (04) :228-233
[6]  
Brown DM, 1996, ARCH SURG-CHICAGO, V131, P1086
[7]  
Chan Albert W., 2001, Curr Interv Cardiol Rep, V3, P149
[8]   EFFECT OF HEPARIN ON THE INHIBITION OF FACTOR-XA BY TISSUE FACTOR PATHWAY INHIBITOR - A SEGMENT, GLY(212)-PHE(243), OF THE 3RD KUNITZ DOMAIN IS A HEPARIN-BINDING SITE [J].
ENJYOJI, K ;
MIYATA, T ;
KAMIKUBO, Y ;
KATO, H .
BIOCHEMISTRY, 1995, 34 (17) :5725-5735
[9]   FUNCTIONAL-SIGNIFICANCE OF THE KUNITZ-TYPE INHIBITORY DOMAINS OF LIPOPROTEIN-ASSOCIATED COAGULATION INHIBITOR [J].
GIRARD, TJ ;
WARREN, LA ;
NOVOTNY, WF ;
LIKERT, KM ;
BROWN, SG ;
MILETICH, JP ;
BROZE, GJ .
NATURE, 1989, 338 (6215) :518-520
[10]   INFLUENCE OF BLOCKADE AT SPECIFIC LEVELS OF THE COAGULATION CASCADE ON RESTENOSIS IN A RABBIT ATHEROSCLEROTIC FEMORAL-ARTERY INJURY MODEL [J].
JANG, YS ;
GUZMAN, LA ;
LINCOFF, AM ;
GOTTSAUNERWOLF, M ;
FORUDI, F ;
HART, CE ;
COURTMAN, DW ;
EZBAN, M ;
ELLIS, SG ;
TOPOL, EJ .
CIRCULATION, 1995, 92 (10) :3041-3050