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 inJournal of thrombosis and haemostasis Vol. 4; no. 11; pp. 2331 - 2339
Main Authors NISHII, Y., GABAZZA, E.C., FUJIMOTO, H., NAKAHARA, H., TAKAGI, T., BRUNO, N., D'ALESSANDRO‐GABAZZA, C. N., MARUYAMA, J., MARUYAMA, K., HAYASHI, T., ADACHI, Y., SUZUKI, K., TAGUCHI, O.
Format Journal Article
LanguageEnglish
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.
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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wiley
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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
URI https://onlinelibrary.wiley.com/doi/abs/10.1111%2Fj.1538-7836.2006.02174.x
https://www.ncbi.nlm.nih.gov/pubmed/17059470
Volume 4
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