THROMBOXANE SYNTHASE INHIBITION AND CARDIOPULMONARY FUNCTION DURING ENDOTOXEMIA IN SHEEP

被引:23
作者
FUJIOKA, K
SUGI, K
ISAGO, T
FLYNN, JT
TRABER, LD
HERNDON, DN
TRABER, DL
机构
[1] UNIV TEXAS,MED BRANCH,DEPT ANESTHESIOL,GALVESTON,TX 77550
[2] UNIV TEXAS,MED BRANCH,DEPT SURG,GALVESTON,TX 77550
[3] UNIV TEXAS,MED BRANCH,DEPT PHYSIOL,GALVESTON,TX 77550
[4] SHRINERS BURN INST,GALVESTON,TX 77550
[5] YAMAGUCHI UNIV,DEPT SURG 1,UBE,YAMAGUCHI 755,JAPAN
[6] THOMAS JEFFERSON UNIV,DEPT PHYSIOL,PHILADELPHIA,PA 19107
关键词
CARDIAC DYSFUNCTION; ENDOTOXIN; END-SYSTOLIC PRESSURE-DIAMETER RELATIONSHIP; SONOMICROMETER; MYOCARDIAL PERFORMANCE; LUNG MICROVASCULAR PERMEABILITY; LUNG-LYMPH FISTULA; SEPSIS;
D O I
10.1152/jappl.1991.71.4.1376
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
We studied the cardiopulmonary response to endotoxin (lipopolysaccharide, LPS) in sheep with and without the administration of a thromboxane synthase inhibitor, OKY-046. The animals were instrumented for crystalographic dimension analysis of the left ventricle (LV) and for measurement of LV, aortic, left atrial, and pulmonary arterial pressures and cardiac index, as well as lung lymph flow. They received 1.0-mu-g/kg of Escherichia coli LPS with (n = 8) and without (n = 8) OKY-046 (10 mg/kg bolus, then 10-mu-g.kg-1.min-1). OKY-046 prevented the increase of pulmonary arterial pressure and the decrease of cardiac index that occurred during the early phase of endotoxemia. Between 8 and 12 h after LPS, cardiac index increased from 6.8 +/- 0.7 to 8.9 +/- 0.51.min-1.m-2. Concomitantly, the end-systolic pressure-diameter relationship (ESPDR, sensitive myocardial contractility index) significantly decreased from 14.7 +/- 0.6 to 7.7 +/- 0.7. Other indexes of the LV contractility (+ dP/dt(max)) were also reduced. OKY-046 prevented the decreases of ESPDR and + dP/dt(max). OKY-046 also attenuated the increased lung lymph flow changes seen with LPS.
引用
收藏
页码:1376 / 1381
页数:6
相关论文
共 28 条
[1]  
BABA H, 1988, J JPN SURG SOC, V89, P6
[2]  
CASEY LC, 1982, J PHARMACOL EXP THER, V222, P441
[3]  
CUNNION RE, 1989, CRIT CARE CLIN, V5, P99
[4]   PULMONARY INJURY AND PROSTAGLANDIN PRODUCTION DURING ENDOTOXEMIA IN CONSCIOUS SHEEP [J].
DEMLING, RH ;
SMITH, M ;
GUNTHER, R ;
FLYNN, JT ;
GEE, MH .
AMERICAN JOURNAL OF PHYSIOLOGY, 1981, 240 (03) :H348-H353
[5]  
FLIGIEL SEG, 1984, AM J PATHOL, V115, P418
[6]   PHOSPHOLIPASE A-2 STIMULATED RELEASE OF PROSTANOIDS FROM THE ISOLATED, PERFUSED RABBIT LIVER - IMPLICATIONS IN REGIONAL CELLULAR INJURY [J].
FLYNN, JT ;
HENRY, JM ;
PERKOWSKI, S .
CANADIAN JOURNAL OF PHYSIOLOGY AND PHARMACOLOGY, 1981, 59 (12) :1268-1273
[7]  
GAAR KA, 1967, AM J PHYSIOL, V213, P910
[8]  
GEE MH, 1986, AM REV RESPIR DIS, V133, P269
[9]   ROLE OF XANTHINE-OXIDASE AND GRANULOCYTES IN ISCHEMIA-REPERFUSION INJURY [J].
GRANGER, DN .
AMERICAN JOURNAL OF PHYSIOLOGY, 1988, 255 (06) :H1269-H1275
[10]  
HERNDON DN, 1990, MULTIPLE ORGAN FAILU, P192