Investigation on vasopeptidase inhibition and its application to pulmonary hypertension
Project/Area Number |
23590123
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Research Category |
Grant-in-Aid for Scientific Research (C)
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Allocation Type | Multi-year Fund |
Section | 一般 |
Research Field |
Biological pharmacy
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Research Institution | Kobe Pharmaceutical University |
Principal Investigator |
EMOTO Noriaki 神戸薬科大学, 薬学部, 教授 (30294218)
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Project Period (FY) |
2011 – 2013
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Project Status |
Completed (Fiscal Year 2013)
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Budget Amount *help |
¥5,330,000 (Direct Cost: ¥4,100,000、Indirect Cost: ¥1,230,000)
Fiscal Year 2013: ¥910,000 (Direct Cost: ¥700,000、Indirect Cost: ¥210,000)
Fiscal Year 2012: ¥1,820,000 (Direct Cost: ¥1,400,000、Indirect Cost: ¥420,000)
Fiscal Year 2011: ¥2,600,000 (Direct Cost: ¥2,000,000、Indirect Cost: ¥600,000)
|
Keywords | エンドセリン / エンドセリン変換酵素 / ブラジキニン / 肺高血圧症 / 肺線維症 / 遺伝子欠損マウス / ブラジキニンニン / ナトリウム利尿ペプチド |
Research Abstract |
We have investigated the possibilities that endothelin-converting enzyme (ECE) is involved in the pathogenesis of pulmonary hypertension and pulmonary fibrosis through other vasoactive peptides in addition to endothelin by using genetically modified mice. We have demonstrated that ECE heterozygous mice were resistant to develop hypoxia-induce pulmonary hypertension by upregulating bradykinin system. We also showed that ECE heterozygous mice were resistant to induce bleomycin-induced pulmonary fibrosis by potentiating CGRP pathway. These results suggest that ECE plays an important role to the pathogenesis of pulmonary hypertension and pulmonary fibrosis, and that ECE may be a plausible target for the therapeutic intervention to these disorders.
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Report
(4 results)
Research Products
(50 results)
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[Journal Article] Michael addition-aromatization reaction of dienylimines bearing a leaving group and its application to the preparation of thiol-selective labeling reagents capable of forming strong carbon-sulfur bonds.2013
Author(s)
Miyoshi M, Aoki Y, Uno Y, Araki M, Kamatani T, Fujii D, Fujita Y, Takeda N, Ueda M, Kitagawa H, Emoto N, Mukai T, Tanaka M, Miyata O.
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Journal Title
J Org Chem.
Volume: 78
Issue: 22
Pages: 11433-11443
DOI
Related Report
Peer Reviewed
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[Journal Article] Activation of Wnt5a-Ror2 signaling associated with epithelial-to-mesenchymal transition (EMT) of tubular epithelial cells during renal fibrosis.2013
Author(s)
Li, X., Yamagata, K., Nishita, M., Endo, M., Arfian, N., Rikitake, Y., Emoto, N., Hirata, K., Tanaka, Y., Minami, Y.
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Journal Title
Genes Cells
Volume: 18
Issue: 7
Pages: 608-619
DOI
Related Report
Peer Reviewed
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[Journal Article] Subsequent Shunt Closure after Targeted Medical Therapy can be an Effective Strategy for Secundum Atrial Septal Defect with Severe Pulmonary Arterial Hypertension.2013
Author(s)
Taniguchi Y, Emoto N, Miyagawa K, Nakayama K, Kinutani H, Tanaka H, Shinke T, Okada K, Okita Y, Hirata, K.
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Journal Title
Heart Vessels.
Volume: 29
Issue: 2
Pages: 282-285
DOI
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Peer Reviewed
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[Journal Article] Differences in hemodynamic parameters and exercise capacity between patients with pulmonary arterial hypertension and chronic heart failure.2012
Author(s)
Nishio R, Tanaka H, Tsuboi Y, Kinutani H, Taniguchi Y, Shigeru M, Toh R, Miura Y, Sakai Y, Emoto N, Kawai H, Hirata K.
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Journal Title
J Cardiopulm Rehabil Prev.
Volume: 32
Issue: 6
Pages: 379-385
DOI
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Peer Reviewed
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[Journal Article] Utility of right ventricular free wall speckle-tracking strain for evaluation of right ventricular performance in patients with pulmonary hypertension.2011
Author(s)
Fukuda Y, Tanaka H, Sugiyama D, Ryo K, Onishi T, Fukuya H, Nogami M, Ohno Y, Emoto N, Kawai H, Hirata K.
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Journal Title
J Am Soc Echocardiogr.
Volume: 24
Pages: 1101-1108
Related Report
Peer Reviewed
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[Presentation] Role of endothelin-converting enzyme-1 inhibition in pulmonary vein remodeling during development of secondary pulmonary hypertension2011
Author(s)
Hartopo AB, Emoto N, Yagi K, Nakayama K, Anggraeni VY, Ali H, Arfian N, Mayasari DS, Nugrahaningsih DAA, Purnomo E, Hirata KI
Organizer
18th Congress of Asia Pacific Society of Cardiology
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