EFFECTS OF HIGH-DOSE INTRACORONARY IRRADIATION ON VASOMOTOR FUNCTION AND SMOOTH-MUSCLE HISTOPATHOLOGY

被引:41
作者
WIEDERMANN, JG
LEAVY, JA
AMOLS, H
SCHWARTZ, A
HOMMA, S
MARBOE, C
WEINBERGER, J
机构
[1] COLUMBIA PRESBYTERIAN MED CTR, CTR INTERVENT CARDIOL, DEPT MED, NEW YORK, NY 10032 USA
[2] COLUMBIA PRESBYTERIAN MED CTR, CTR INTERVENT CARDIOL, DEPT RADIAT ONCOL, NEW YORK, NY 10032 USA
[3] COLUMBIA PRESBYTERIAN MED CTR, CARDIAC PATHOL SECT, NEW YORK, NY 10032 USA
[4] COLUMBIA UNIV, NEW YORK, NY 10032 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY | 1994年 / 267卷 / 01期
关键词
PORCINE MODEL; ENDOTHELIAL FUNCTION; INTRAVASCULAR ULTRASOUND; RESTENOSIS;
D O I
10.1152/ajpheart.1994.267.1.H125
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
A significant component of restenosis after coronary angioplasty is due to medial proliferation. Targeted ablation of the proliferating cells by ionizing radiation may prevent restenosis. We delivered high-dose intracoronary gamma-irradiation in porcine coronary arteries and assessed vasomotor function acutely and at 32 days, with pathological analysis at 32 days. Changes in luminal area were assessed by intravascular ultrasound. Irradiated segments acutely displayed vasoconstriction to acetylcholine, with loss of smooth muscle response to nitroglycerin. Restudy revealed restoration of normal vasodilatory response to acetylcholine but persistent loss of response to nitroglycerin. Histopathology at 32 days revealed minor neointima formation without luminal compromise and diffuse fibrosis of the smooth muscle layer. The surrounding myocardium was normal. Focal medial fibrosis without significant endothelial or myocardial damage can be achieved via this technique; intracoronary irradiation, therefore, may be an effective way of impairing the restenosis process.
引用
收藏
页码:H125 / H132
页数:8
相关论文
共 32 条
[1]   INTIMAL PROLIFERATION OF SMOOTH-MUSCLE CELLS AS AN EXPLANATION FOR RECURRENT CORONARY-ARTERY STENOSIS AFTER PERCUTANEOUS TRANS-LUMINAL CORONARY ANGIOPLASTY [J].
AUSTIN, GE ;
RATLIFF, NB ;
HOLLMAN, J ;
TABEI, S ;
PHILLIPS, DF .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 1985, 6 (02) :369-375
[2]   ENDOTHELIUM-DEPENDENT VASCULAR-RESPONSES - MEDIATORS AND MECHANISMS [J].
BRENNER, BM ;
TROY, JL ;
BALLERMANN, BJ .
JOURNAL OF CLINICAL INVESTIGATION, 1989, 84 (05) :1373-1378
[3]   THE MECHANISMS OF NITROGLYCERIN ACTION - STENOSIS VASODILATATION AS A MAJOR COMPONENT OF THE DRUG RESPONSE [J].
BROWN, BG ;
BOLSON, E ;
PETERSEN, RB ;
PIERCE, CD ;
DODGE, HT .
CIRCULATION, 1981, 64 (06) :1089-1097
[4]   SIGNIFICANCE OF QUIESCENT SMOOTH-MUSCLE MIGRATION IN THE INJURED RAT CAROTID-ARTERY [J].
CLOWES, AW ;
SCHWARTZ, SM .
CIRCULATION RESEARCH, 1985, 56 (01) :139-145
[5]   2 MECHANISMS MEDIATE RELAXATION BY BRADYKININ OF PIG CORONARY-ARTERY - NO-DEPENDENT AND NO-INDEPENDENT RESPONSES [J].
COWAN, CL ;
COHEN, RA .
AMERICAN JOURNAL OF PHYSIOLOGY, 1991, 261 (03) :H830-H835
[6]  
COWAN CL, 1992, J PHARMACOL EXP THER, V260, P248
[7]  
ELIAS JM, 1989, AM J CLIN PATHOL, V92, P836
[8]  
FAJARDO LF, 1988, PATHOL ANNU, V23, P297
[9]  
Fletcher G, 1980, TXB RADIOTHERAPY
[10]   THE OBLIGATORY ROLE OF ENDOTHELIAL-CELLS IN THE RELAXATION OF ARTERIAL SMOOTH-MUSCLE BY ACETYLCHOLINE [J].
FURCHGOTT, RF ;
ZAWADZKI, JV .
NATURE, 1980, 288 (5789) :373-376