Endothelin receptor blockade prevents the rise in pulmonary vascular resistance after cardiopulmonary bypass in lambs with increased pulmonary blood flow

被引:24
作者
Petrossian, E
Parry, AJ
Reddy, VM
Akkersdijk, GP
McMullan, DM
Thompson, L
Hendricks-Munoz, KD
Hallak, H
Hanley, FL
Fineman, JR
机构
[1] Univ Calif San Francisco, Dept Cardiothorac Surg, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Dept Pediat, San Francisco, CA 94143 USA
[3] NYU, Dept Pediat, New York, NY 10016 USA
[4] Warner Lambert Parke Davis, Parke Davis Pharmaceut Res, Dept Metab & Pharmacokinet, Ann Arbor, MI 48105 USA
关键词
D O I
10.1016/S0022-5223(99)70429-0
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Children,vith increased pulmonary blood flow may experience morbidity as the result of increased pulmonary vascular resistance after operations in which cardiopulmonary bypass is used. Plasma levels of endothelin-1, a potent vasoactive substance implicated in pulmonary hypertension, are increased after cardiopulmonary bypass. Objectives: In a lamb model of increased pulmonary blood flow after in utero placement of an aortopulmonary shunt, we characterized the changes in pulmonary vascular resistance induced by hypothermic cardiopulmonary bypass and investigated the role of endothelin-l and endothelin-a receptor activation in postbypass pulmonary hypertension. Methods: Tn eleven 1-month-old lambs, the shunt was closed, and vascular pressures and blood flows were monitored. An infusion of a selective endothelin-A receptor blocker (PD 156707; 1.0 mg/kg/h) or drug vehicle (saline solution) was then begun 30 minutes before cardiopulmonary bypass and continued for 4 hours after bypass. The hemodynamic variables were monitored, and plasma endothelin-1 concentrations were determined before, during, and for 6 hours after cardiopulmonary bypass. Results: After 90 minutes of hypothermic cardiopulmonary bypass, both pulmonary arterial pressure and pulmonary vascular resistance increased significantly in saline-treated lambs during the 6-hour study period (P <.05), In lambs pretreated with PD 156707, pulmonary arterial pressure and pulmonary vascular resistance decreased (P <.05) After bypass, plasma endothelin-1 concentrations increased in all lambs: there was a positive correlation between postbypass pulmonary vascular resistance and plasma endothelin-1 concentrations (P <.05), Conclusions: This study suggests that endothelin-A receptor-induced pulmonary vasoconstriction mediates, in part, the rise in pulmonary vascular resistance after cardiopulmonary bypass. Endothelin-A receptor antagonists may decrease morbidity in children at risk for postbypass pulmonary hypertension. This potential therapy warrants further investigation.
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收藏
页码:314 / 322
页数:9
相关论文
共 30 条
[1]   ULTRASTRUCTURAL-CHANGES IN THE HUMAN-LUNG FOLLOWING CARDIOPULMONARY BYPASS [J].
ANYANWU, E ;
DITTRICH, H ;
GIESEKING, R ;
ENDERS, HJ .
BASIC RESEARCH IN CARDIOLOGY, 1982, 77 (03) :309-322
[2]  
Black Stephen M., 1996, Pediatric Research, V39, p23A
[3]   PULMONARY-HYPERTENSION IN CHILDREN - PERIOPERATIVE MANAGEMENT [J].
BURROWS, FA ;
KLINCK, JR ;
RABINOVITCH, M ;
BOHN, DJ .
CANADIAN ANAESTHETISTS SOCIETY JOURNAL, 1986, 33 (05) :606-628
[4]  
Castaneda AR, 1994, CARDIAC SURG NEONATE, P23
[5]   EFFECT OF AN ENDOTHELIN-RECEPTOR ANTAGONIST ON ISCHEMIC ACUTE-RENAL-FAILURE [J].
CHAN, L ;
CHITTINANDANA, A ;
SHAPIRO, JI ;
SHANLEY, PF ;
SCHRIER, RW .
AMERICAN JOURNAL OF PHYSIOLOGY, 1994, 266 (01) :F135-F138
[6]  
Chenoweth DE, 1981, NEW ENGL J MED, V304, P487
[7]  
FINEMAN JR, 1995, ANNU REV PHYSIOL, V57, P115
[8]   WHY ARE CIRCULATING CONCENTRATIONS OF ENDOTHELIN-1 SO LOW [J].
FRELIN, C ;
GUEDIN, D .
CARDIOVASCULAR RESEARCH, 1994, 28 (11) :1613-1622
[9]   RAISED PLASMA ENDOTHELIN-I CONCENTRATION FOLLOWING COLD PRESSOR TEST [J].
FYHRQUIST, F ;
SAIJONMAA, O ;
METSARINNE, K ;
TIKKANEN, I ;
ROSENLOF, K ;
TIKKANEN, T .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1990, 169 (01) :217-221
[10]   EXPRESSION OF ENDOTHELIN-1 IN THE LUNGS OF PATIENTS WITH PULMONARY-HYPERTENSION [J].
GIAID, A ;
YANAGISAWA, M ;
LANGLEBEN, D ;
MICHEL, RP ;
LEVY, R ;
SHENNIB, H ;
KIMURA, S ;
MASAKI, T ;
DUGUID, WP ;
STEWART, DJ .
NEW ENGLAND JOURNAL OF MEDICINE, 1993, 328 (24) :1732-1739