Protective role of protein C inhibitor in monocrotaline‐induced pulmonary hypertension
Background: Protein C inhibitor (PCI) plays a role in multiple biological processes including fertilization, coagulation, fibrinolysis and kinin systems. Objectives: We hypothesized that PCI participates in the pathogenesis of pulmonary hypertension. To demonstrate this, we compared the development...
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Published in | Journal of thrombosis and haemostasis Vol. 4; no. 11; pp. 2331 - 2339 |
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Main Authors | , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Oxford, UK
Blackwell Publishing Ltd
01.11.2006
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Abstract | Background: Protein C inhibitor (PCI) plays a role in multiple biological processes including fertilization, coagulation, fibrinolysis and kinin systems. Objectives: We hypothesized that PCI participates in the pathogenesis of pulmonary hypertension. To demonstrate this, we compared the development of pulmonary hypertension in mice overexpressing PCI in the lung with wild‐type (WT) mice. Pulmonary hypertension was induced by s.c. injection of 600 mg kg−1 of monocrotaline weekly for 8 weeks. Results: Right ventricular arterial pressure was significantly increased in monocrotaline‐treated WT mice compared with that in monocrotaline‐treated transgenic mice. Bronchoalveolar lavage fluid (BALF) levels of thrombin–antithrombin complex, monocyte chemoattractant protein‐1 and platelet‐derived growth factor, and the plasma level of tumor necrosis factor‐α were significantly increased in monocrotaline‐treated WT mice as compared with monocrotaline‐treated PCI transgenic mice. Increased level of PCI‐thrombin complex was detected in BALF from monocrotaline‐treated PCI transgenic mice as compared with saline‐treated PCI transgenic mice. Conclusions: This study showed that increased expression of PCI in the lung is protective against monocrotaline‐induced pulmonary hypertension, suggesting a potential beneficial effect of PCI for the therapy of this disease. |
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AbstractList | Protein C inhibitor (PCI) plays a role in multiple biological processes including fertilization, coagulation, fibrinolysis and kinin systems.
We hypothesized that PCI participates in the pathogenesis of pulmonary hypertension. To demonstrate this, we compared the development of pulmonary hypertension in mice overexpressing PCI in the lung with wild-type (WT) mice. Pulmonary hypertension was induced by s.c. injection of 600 mg kg-1 of monocrotaline weekly for 8 weeks.
Right ventricular arterial pressure was significantly increased in monocrotaline-treated WT mice compared with that in monocrotaline-treated transgenic mice. Bronchoalveolar lavage fluid (BALF) levels of thrombin-antithrombin complex, monocyte chemoattractant protein-1 and platelet-derived growth factor, and the plasma level of tumor necrosis factor-alpha were significantly increased in monocrotaline-treated WT mice as compared with monocrotaline-treated PCI transgenic mice. Increased level of PCI-thrombin complex was detected in BALF from monocrotaline-treated PCI transgenic mice as compared with saline-treated PCI transgenic mice.
This study showed that increased expression of PCI in the lung is protective against monocrotaline-induced pulmonary hypertension, suggesting a potential beneficial effect of PCI for the therapy of this disease. Background: Protein C inhibitor (PCI) plays a role in multiple biological processes including fertilization, coagulation, fibrinolysis and kinin systems. Objectives: We hypothesized that PCI participates in the pathogenesis of pulmonary hypertension. To demonstrate this, we compared the development of pulmonary hypertension in mice overexpressing PCI in the lung with wild‐type (WT) mice. Pulmonary hypertension was induced by s.c. injection of 600 mg kg−1 of monocrotaline weekly for 8 weeks. Results: Right ventricular arterial pressure was significantly increased in monocrotaline‐treated WT mice compared with that in monocrotaline‐treated transgenic mice. Bronchoalveolar lavage fluid (BALF) levels of thrombin–antithrombin complex, monocyte chemoattractant protein‐1 and platelet‐derived growth factor, and the plasma level of tumor necrosis factor‐α were significantly increased in monocrotaline‐treated WT mice as compared with monocrotaline‐treated PCI transgenic mice. Increased level of PCI‐thrombin complex was detected in BALF from monocrotaline‐treated PCI transgenic mice as compared with saline‐treated PCI transgenic mice. Conclusions: This study showed that increased expression of PCI in the lung is protective against monocrotaline‐induced pulmonary hypertension, suggesting a potential beneficial effect of PCI for the therapy of this disease. |
Author | MARUYAMA, K. MARUYAMA, J. GABAZZA, E.C. BRUNO, N. NISHII, Y. FUJIMOTO, H. SUZUKI, K. HAYASHI, T. D'ALESSANDRO‐GABAZZA, C. N. TAKAGI, T. ADACHI, Y. TAGUCHI, O. NAKAHARA, H. |
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Snippet | Background: Protein C inhibitor (PCI) plays a role in multiple biological processes including fertilization, coagulation, fibrinolysis and kinin systems.... Protein C inhibitor (PCI) plays a role in multiple biological processes including fertilization, coagulation, fibrinolysis and kinin systems. We hypothesized... |
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SubjectTerms | Animals Bronchoalveolar Lavage Fluid coagulation fibrinolysis Humans Hypertension, Pulmonary - chemically induced Hypertension, Pulmonary - drug therapy Hypertension, Pulmonary - genetics Hypertension, Pulmonary - metabolism Hypertension, Pulmonary - pathology Hypertension, Pulmonary - prevention & control Intercellular Signaling Peptides and Proteins - metabolism Lung - metabolism Lung - pathology Mice Mice, Transgenic Monocrotaline - pharmacology Monocrotaline - toxicity Protein C Inhibitor - genetics Protein C Inhibitor - metabolism Protein C Inhibitor - therapeutic use protein C pathway pulmonary hypertension Thrombin - metabolism |
Title | Protective role of protein C inhibitor in monocrotaline‐induced pulmonary hypertension |
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