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 3h. APAE rats developed a higher right ventricular systolic pressure (RVSP), lower mean arterial blood pressure (MABP), and had lower PaO2. At 3h, 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 10–25min) 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.
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September 2002
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Conference Article|
September 01 2002
Effects of a selective endothelin A receptor antagonist, ABT-627, in healthy normotensive anaesthetized rats developing acute pulmonary air embolism
Bilal AYACH;
Bilal AYACH
*Laval Hospital Research Center, Quebec Heart & Lung Institute, Department of Medicine, Laval University, 2725 Chemin Ste-Foy, Ste-Foy, QC G1V 4G5, Canada
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John TSANG;
John TSANG
†Department of Medicine, University of British Columbia, Pulmonary Research Laboratories, St Paul's Hospital, 1081 Burrard Street, Vancouver, BC V6Z 1Y6, Canada
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Arco Y. JENG;
Arco Y. JENG
‡Metabolic and Cardiovascular Diseases, Novartis Institute for Biomedical Research, Novartis Pharmaceuticals, 556 Morris Avenue, Summit, NJ 07901-1398, U.S.A.
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André BLOUIN;
André BLOUIN
*Laval Hospital Research Center, Quebec Heart & Lung Institute, Department of Medicine, Laval University, 2725 Chemin Ste-Foy, Ste-Foy, QC G1V 4G5, Canada
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Mélanie GOSSELIN;
Mélanie GOSSELIN
*Laval Hospital Research Center, Quebec Heart & Lung Institute, Department of Medicine, Laval University, 2725 Chemin Ste-Foy, Ste-Foy, QC G1V 4G5, Canada
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Fu-Hou WANG;
Fu-Hou WANG
‡Metabolic and Cardiovascular Diseases, Novartis Institute for Biomedical Research, Novartis Pharmaceuticals, 556 Morris Avenue, Summit, NJ 07901-1398, U.S.A.
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Jinshyun R. WU-WONG;
Jinshyun R. WU-WONG
§Abbott Laboratories Inc., Pharmaceutical Products Division, 100 Abbott Park Rd, Chicago, IL 60064-3500, U.S.A.
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Jerry WESSALE;
Jerry WESSALE
§Abbott Laboratories Inc., Pharmaceutical Products Division, 100 Abbott Park Rd, Chicago, IL 60064-3500, U.S.A.
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Terry J. OPGENORTH;
Terry J. OPGENORTH
§Abbott Laboratories Inc., Pharmaceutical Products Division, 100 Abbott Park Rd, Chicago, IL 60064-3500, U.S.A.
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Bruno BATTISTINI
*Laval Hospital Research Center, Quebec Heart & Lung Institute, Department of Medicine, Laval University, 2725 Chemin Ste-Foy, Ste-Foy, QC G1V 4G5, Canada
Dr B. Battistini (e-mail [email protected]).
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Publisher: Portland Press Ltd
Online ISSN: 1470-8736
Print ISSN: 0143-5221
© 2002 The Biochemical Society and the Medical Research Society
2002
Clin Sci (Lond) (2002) 103 (s2002): 371S–375S.
Citation
Bilal AYACH, John TSANG, Arco Y. JENG, André BLOUIN, Mélanie GOSSELIN, Fu-Hou WANG, Jinshyun R. WU-WONG, Jerry WESSALE, Terry J. OPGENORTH, Bruno BATTISTINI; Effects of a selective endothelin A receptor antagonist, ABT-627, in healthy normotensive anaesthetized rats developing acute pulmonary air embolism. Clin Sci (Lond) 1 September 2002; 103 (s2002): 371S–375S. doi: https://doi.org/10.1042/CS103S371S
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