Inhibition of smooth muscle cell proliferation after local drug delivery of the antimitotic drug paclitaxel using a porous balloon catheter

被引:54
作者
Oberhoff, M [1 ]
Kunert, W
Herdeg, C
Küttner, A
Kranzhöfer, A
Horch, B
Baumbach, A
Karsch, KR
机构
[1] Univ Bristol, Bristol Royal Infirm, Inst Heart, Bristol BS2 8HW, Avon, England
[2] Univ Tubingen, Div Cardiol, Dept Med, D-72076 Tubingen, Germany
关键词
paclitaxel; local drug delivery; PTCA; restenosis; smooth muscle cell; rabbits;
D O I
10.1007/s003950170058
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Bristol Royal Infirmary Percutaneous transluminal coronary angioplasty is an accepted treatment fbr coronary artery disease. The major limitation, however, is the high incidence of restenosis which limits the long-term benefit of this intervention. Paclitaxel is a new antiproliferative agent that has generated considerable scientific interest since it was introduced in clinical trials in the early 1980s. Recent in vitro studies have shown that paclitaxel has considerable antiproliferative activity in human coculture systems. In the present study the efficacy of paclitaxel was investigated after development of an intimal plaque by electrical stimulation and additional cholesterol diet and subsequent balloon angioplasty in 63 New Zealand White rabbits. Local drug delivery of paclitaxel was accomplished in 30 rabbits with a porous balloon catheter (35 holes, hole diameter 75 mum, 2 5 mm catheter diameter). Paclitaxel was administered locally with 4 ml (solution 10(-5) mol/L) using an injection pressure of 2 atm. To study the extent of restenosis and morphological changes, the animals were sacrificed 7, 28 or 56 days after intervention. After staining procedures quantification of SMC proliferation, intimal macrophages and morphological analyses were performed. Paclitaxel plasma concentrations were measured using HPLC technique. One week after balloon angioplasty the arteries treated with local paclitaxel delivery showed an insignificant trend towards a reduction in intimal smooth muscle cell proliferation (untreated 8.4 +/- 4.9 % vs paclitaxel treated 2.4 +/- 2.4 %, p = NS). However, this resulted Bristol Royal Infirmary in a significant reduction of stenosis degree of 66 % 8 weeks after intervention compared to the untreated group (untreated 41 +/- 18 % vs paclitaxel treated 14 +/- 11 %, p = 0.005). In conclusion, locally delivered paclitaxel prevented neointimal thickening in the rabbit carotid artery after balloon angioplasty. Local paclitaxel treatment may therefore be a clinical option for the prevention of restenosis after coronary interventions. However, further preclinical studies have to prove long-term efficacy and safety.
引用
收藏
页码:275 / 282
页数:8
相关论文
共 36 条
[1]  
Axel DI, 1997, CIRCULATION, V96, P636
[2]  
Baumbach A, 1999, CATHETER CARDIO INTE, V47, P102, DOI 10.1002/(SICI)1522-726X(199905)47:1<102::AID-CCD22>3.0.CO
[3]  
2-G
[4]   Local delivery of a low molecular weight heparin following stent implantation in the pig coronary artery [J].
Baumbach, A ;
Oberhoff, M ;
Herdeg, C ;
Lerch, M ;
Schröder, S ;
Meisner, C ;
Rübsamen, K ;
Karsch, KR .
BASIC RESEARCH IN CARDIOLOGY, 2000, 95 (03) :173-178
[5]   RESPONSES OF VESSEL WALLS TO CHRONICALLY APPLIED ELECTRICAL STIMULI [J].
BETZ, E ;
SCHLOTE, W .
BASIC RESEARCH IN CARDIOLOGY, 1979, 74 (01) :10-20
[6]   EFFECT OF MICROTUBULE-SPECIFIC DRUGS UPON SPATIAL-ORGANIZATION OF EXTRACELLULAR-MATRIX IN FIBROBLASTIC CULTURES [J].
DOMNINA, LV ;
IVANOVA, OY ;
VASILIEV, JM .
CELL BIOLOGY INTERNATIONAL, 1995, 19 (09) :743-748
[7]   NONLINEAR PHARMACOKINETICS AND METABOLISM OF PACLITAXEL AND ITS PHARMACOKINETIC/PHARMACODYNAMIC RELATIONSHIPS IN HUMANS [J].
GIANNI, L ;
KEARNS, CM ;
GIANI, A ;
CAPRI, G ;
VIGANO, L ;
LOCATELLI, A ;
BONADONNA, G ;
EGORIN, MJ .
JOURNAL OF CLINICAL ONCOLOGY, 1995, 13 (01) :180-190
[8]   DISTRIBUTION OF MICROTUBULE ORGANIZING CENTERS IN MIGRATING SHEETS OF ENDOTHELIAL-CELLS [J].
GOTLIEB, AI ;
MAY, LM ;
SUBRAHMANYAN, L ;
KALNINS, VI .
JOURNAL OF CELL BIOLOGY, 1981, 91 (02) :589-594
[9]   ACCUMULATION OF MACROPHAGES IN THE ARTERIAL VESSEL WALL FOLLOWING EXPERIMENTAL BALLOON ANGIOPLASTY [J].
HANKE, H ;
HASSENSTEIN, S ;
ULMER, A ;
KAMENZ, J ;
OBERHOFF, M ;
HAASE, KK ;
BAUMBACH, A ;
GOWN, AM ;
KARSCH, KR .
EUROPEAN HEART JOURNAL, 1994, 15 (05) :691-698
[10]   TIME COURSE OF SMOOTH-MUSCLE CELL-PROLIFERATION IN THE INTIMA AND MEDIA OF ARTERIES FOLLOWING EXPERIMENTAL ANGIOPLASTY [J].
HANKE, H ;
STROHSCHNEIDER, T ;
OBERHOFF, M ;
BETZ, E ;
KARSCH, KR .
CIRCULATION RESEARCH, 1990, 67 (03) :651-659