Effects of a selective endothelin A receptor antagonist, ABT-627, in healthy normotensive anaesthetized rats developing acute pulmonary air embolism

被引:5
作者
Ayach, B
Tsang, J
Jeng, AY
Blouin, A
Gosselin, M
Wang, FH
Wu-Wong, JYR
Wessale, J
Opgenorth, TJ
Battistini, B
机构
[1] Univ Laval, Dept Med, Quebec Heart & Lung Inst, Laval Hosp Res Ctr, Ste Foy, PQ G1V 4G5, Canada
[2] Univ British Columbia, Pulm Res Labs, St Pauls Hosp, Dept Med, Vancouver, BC V6Z 1Y6, Canada
[3] Novartis Pharmaceut, Novartis Inst Biomed Res, Metab & Cardiovasc Dis, Summit, NJ 07901 USA
[4] Abbott Labs, Div Pharmaceut Prod, Abbott Pk, IL 60064 USA
关键词
pulmonary; air embolism; hypertension; blood pressure; endothelin; ETA receptor; gene expression;
D O I
10.1042/CS103S371S
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Acute pulmonary air embolism (APAE) injures the vascular endothelium in the lung and results in pulmonary hypertension (PH). Endothelins (ETs), a family of potent vasoactive peptides, are known to be associated with PH of various aetiologies. We evaluated the effects of ABT-627, a selective ETA receptor (ETA-R) antagonist in a rat model of APAE over 3 h. APAE rats developed a higher right ventricular systolic pressure (RVSP), lower mean arterial blood pressure (MABP), and had lower PaO2. At 3 h, arterial plasma levels of ET-1 were increased. ABT-627-treated controls showed no effects. However, ABT-627 significantly lowered RVSP during APAE, abolished the short recovery phase (within 10-25 min) of MABP without affecting the subsequent lowering of MABP, and improved oxygen saturation in APAE rats. These results show that ETA-R subtype is involved in the pathogenesis of APAE since a blockade of this receptor subtype attenuated the cardiopulmonary deterioration and improved blood gas exchanges in rats with this disease.
引用
收藏
页码:371S / 375S
页数:5
相关论文
共 20 条
[11]   The role of endothelin-1 as a mediator of the pressure response after air embolism in blood perfused lungs [J].
Schmeck, J ;
Koch, T ;
Patt, B ;
Heller, A ;
Neuhof, H ;
van Ackern, K .
INTENSIVE CARE MEDICINE, 1998, 24 (06) :605-611
[12]   Pathophysiology and treatment of haemodynamic instability in acute pulmonary embolism: the pivotal role of pulmonary vasoconstriction [J].
Smulders, YM .
CARDIOVASCULAR RESEARCH, 2000, 48 (01) :23-33
[13]   Contribution of pulmonary vasoconstriction to haemodynamic instability after acute pulmonary embolism - Implications for treatment? [J].
Smulders, YM .
NETHERLANDS JOURNAL OF MEDICINE, 2001, 58 (06) :241-247
[14]   Endothelin abnormalities in patients with pulmonary embolism [J].
Sofia, M ;
Faraone, S ;
Alifano, M ;
Micco, A ;
Albisinni, R ;
MAniscalco, M ;
DiMinno, G .
CHEST, 1997, 111 (03) :544-549
[15]   INCREASED LUNG ENDOTHELIN-1 PRODUCTION IN RATS WITH IDIOPATHIC PULMONARY-HYPERTENSION [J].
STELZNER, TJ ;
OBRIEN, RF ;
YANAGISAWA, M ;
SAKURAI, T ;
SATO, K ;
WEBB, S ;
ZAMORA, M ;
MCMURTRY, IF ;
FISHER, JH .
AMERICAN JOURNAL OF PHYSIOLOGY, 1992, 262 (05) :L614-L620
[16]   The hemodynamic effects of endothelin receptor antagonism during a venous air infusion in dogs [J].
Tanus-Santos, JE ;
Gordo, WM ;
Udelsmann, A ;
Moreno, H .
ANESTHESIA AND ANALGESIA, 2000, 90 (01) :102-106
[17]   Nonselective endothelin-receptor antagonism attenuates hemodynamic changes after massive pulmonary air embolism in dogs [J].
Tanus-Santos, JE ;
Gordo, WM ;
Udelsmann, A ;
Cittadino, MH ;
Moreno, H .
CHEST, 2000, 118 (01) :175-179
[18]   Biphasic release of immunoreactive endothelins following acute pulmonary thromboembolism in pigs [J].
Tsang, J ;
Battistini, S ;
Dussault, P ;
Stewart, K ;
Qayumi, KA .
JOURNAL OF CARDIOVASCULAR PHARMACOLOGY, 2000, 36 :S221-S224
[19]   ENDOTHELIN ET(A) AND ET(B) RECEPTORS MEDIATE VASCULAR SMOOTH-MUSCLE CONTRACTION [J].
WHITE, DG ;
CANNON, TR ;
GARRATT, H ;
MUNDIN, JW ;
SUMNER, MJ ;
WATTS, IS .
JOURNAL OF CARDIOVASCULAR PHARMACOLOGY, 1993, 22 :S144-S148
[20]   2,4-diarylpyrrolidine-3-carboxylic acids potent ETA selective endothelin receptor antagonists .1. Discovery of A-127722 [J].
Winn, M ;
vonGeldern, TW ;
Opgenorth, TJ ;
Jae, HS ;
Tasker, AS ;
Boyd, SA ;
Kester, JA ;
Mantei, RA ;
Bal, R ;
Sorensen, BK ;
WuWong, JR ;
Chiou, WJ ;
Dixon, DB ;
Novosad, EI ;
Hernandez, L ;
Marsh, KC .
JOURNAL OF MEDICINAL CHEMISTRY, 1996, 39 (05) :1039-1048