FREQUENCY AND SEVERITY OF CYCLIC FLOW ALTERNATIONS AND PLATELET-AGGREGATION PREDICT THE SEVERITY OF NEOINTIMAL PROLIFERATION FOLLOWING EXPERIMENTAL CORONARY STENOSIS AND ENDOTHELIAL INJURY

被引:130
作者
WILLERSON, JT
YAO, SK
MCNATT, J
BENEDICT, CR
ANDERSON, HV
GOLINO, P
MURPHREE, SS
BUJA, LM
机构
[1] UNIV TEXAS, SCH MED, DEPT PATHOL, HOUSTON, TX 77030 USA
[2] TEXAS HEART INST, HOUSTON, TX 77025 USA
[3] UNIV TEXAS, HLTH SCI CTR, SW MED SCH, DEPT PATHOL, DALLAS, TX 75235 USA
[4] UNIV NAPLES 2, SCH MED, DIV CARDIOL, I-80131 NAPLES, ITALY
关键词
THROMBOXANE-A2; SEROTONIN; RESTENOSIS;
D O I
10.1073/pnas.88.23.10624
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The role of recurrent platelet aggregation in the development of neointimal proliferation of coronary arteries was explored in this study, and the hypothesis was evaluated that recurrent platelet aggregation and the consequent frequency and severity of cyclic coronary blood flow variations are important pathophysiologic factors in the subsequent development of neointimal proliferation. In 24 chronically instrumented dogs, variable degrees of coronary artery neointimal proliferation were observed 3 weeks after mechanical injury of the arterial endothelium and the placement of an external coronary artery constrictor. The severity of neointimal proliferation at 21 days was closely related to the frequency and severity of cyclic coronary blood flow variations during the initial 7 days after instrumentation of the animals, itself a manifestation of recurrent platelet aggregation and dislodgement. Pharmacological therapy with a dual thromboxane A2 synthetase inhibitor and receptor antagonist and with a serotonin S2 receptor antagonist frequently was successful in abolishing cyclic blood flow variations and in retarding neointimal proliferation.
引用
收藏
页码:10624 / 10628
页数:5
相关论文
共 40 条
[1]   CYCLIC CORONARY-ARTERY FLOW IN DOGS AFTER CORONARY ANGIOPLASTY [J].
ANDERSON, HV ;
YAO, SK ;
MURPHREE, SS ;
BUJA, LM ;
MCNATT, JM ;
WILLERSON, JT .
CORONARY ARTERY DISEASE, 1990, 1 (06) :717-723
[2]   SEROTONIN AS A MEDIATOR OF CYCLIC FLOW VARIATIONS IN STENOSED CANINE CORONARY-ARTERIES [J].
ASHTON, JH ;
BENEDICT, CR ;
FITZGERALD, C ;
RAHEJA, S ;
TAYLOR, A ;
CAMPBELL, WB ;
BUJA, LM ;
WILLERSON, JT .
CIRCULATION, 1986, 73 (03) :572-578
[3]   COOPERATIVE MEDIATION BY SEROTONIN-S2 AND THROMBOXANE-A2 PROSTAGLANDIN-H2 RECEPTOR ACTIVATION OF CYCLIC FLOW VARIATIONS IN DOGS WITH SEVERE CORONARY-ARTERY STENOSES [J].
ASHTON, JH ;
OGLETREE, ML ;
MICHEL, IM ;
GOLINO, P ;
MCNATT, JM ;
TAYLOR, AL ;
RAHEJA, S ;
SCHMITZ, J ;
BUJA, LM ;
CAMPBELL, WB ;
WILLERSON, JT .
CIRCULATION, 1987, 76 (04) :952-959
[4]   INHIBITION OF CYCLIC FLOW VARIATIONS IN STENOSED CANINE CORONARY-ARTERIES BY THROMBOXANE-A2 PROSTAGLANDIN-H2 RECEPTOR ANTAGONISTS [J].
ASHTON, JH ;
SCHMITZ, JM ;
CAMPBELL, WB ;
OGLETREE, ML ;
RAHEJA, S ;
TAYLOR, AL ;
FITZGERALD, C ;
BUJA, LM ;
WILLERSON, JT .
CIRCULATION RESEARCH, 1986, 59 (05) :568-578
[5]   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
[6]   MORPHOLOGY AFTER TRANS-LUMINAL ANGIOPLASTY IN HUMAN-BEINGS [J].
BLOCK, PC ;
MYLER, RK ;
STERTZER, S ;
FALLON, JT .
NEW ENGLAND JOURNAL OF MEDICINE, 1981, 305 (07) :382-385
[7]   EFFECTS OF THE SELECTIVE THROMBOXANE SYNTHETASE INHIBITOR DAZOXIBEN ON VARIATIONS IN CYCLIC BLOOD-FLOW IN STENOSED CANINE CORONARY-ARTERIES [J].
BUSH, LR ;
CAMPBELL, WB ;
BUJA, LM ;
TILTON, GD ;
WILLERSON, JT .
CIRCULATION, 1984, 69 (06) :1161-1170
[8]   MECHANISMS OF ARTERIAL GRAFT FAILURE - THE ROLE OF CELLULAR PROLIFERATION [J].
CLOWES, AW ;
REIDY, MA .
ANNALS OF THE NEW YORK ACADEMY OF SCIENCES, 1987, 516 :673-678
[9]  
CLOWES AW, 1983, LAB INVEST, V49, P208
[10]  
COHEN ML, 1983, J PHARMACOL EXP THER, V227, P327