Angiotensin Blockade Inhibits Osteopontin Expression in Non-infarcted Myocardium After Myocardial Infarction

Osteopontin has been reported to have an important role in cardiac fibrosis. However, little is known about the effects of angiotensin-converting enzyme inhibitor (ACEI) and angiotensin type 1 receptor blockers (ARB) on osteopontin expression in infarcted myocardium. The purpose of this study was to...

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Main Authors: Takanori Kusuyama, Minoru Yoshiyama, Takashi Omura, Daisuke Nishiya, Soichiro Enomoto, Ryo Matsumoto, Yasukatsu Izumi, Kaname Akioka, Kazuhide Takeuchi, Hiroshi Iwao, Junichi Yoshikawa
Format: Article
Language:English
Published: Elsevier 2005-01-01
Series:Journal of Pharmacological Sciences
Online Access:http://www.sciencedirect.com/science/article/pii/S1347861319321814
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spelling doaj-fc7f8e6bd66140ce963fa1154e527c5f2020-11-25T01:10:30ZengElsevierJournal of Pharmacological Sciences1347-86132005-01-01983283289Angiotensin Blockade Inhibits Osteopontin Expression in Non-infarcted Myocardium After Myocardial InfarctionTakanori Kusuyama0Minoru Yoshiyama1Takashi Omura2Daisuke Nishiya3Soichiro Enomoto4Ryo Matsumoto5Yasukatsu Izumi6Kaname Akioka7Kazuhide Takeuchi8Hiroshi Iwao9Junichi Yoshikawa10Department of Internal Medicine and Cardiology, Osaka City University Graduate School of Medicine, 1-4-3 Asahi-machi, Abeno-ku, Osaka 545-8585, JapanDepartment of Internal Medicine and Cardiology, Osaka City University Graduate School of Medicine, 1-4-3 Asahi-machi, Abeno-ku, Osaka 545-8585, Japan; Corresponding author. FAX: +81-6-6646-6808 E-mail: yoshiyama@med.osaka-cu.ac.jpDepartment of Internal Medicine and Cardiology, Osaka City University Graduate School of Medicine, 1-4-3 Asahi-machi, Abeno-ku, Osaka 545-8585, JapanDepartment of Internal Medicine and Cardiology, Osaka City University Graduate School of Medicine, 1-4-3 Asahi-machi, Abeno-ku, Osaka 545-8585, JapanDepartment of Internal Medicine and Cardiology, Osaka City University Graduate School of Medicine, 1-4-3 Asahi-machi, Abeno-ku, Osaka 545-8585, JapanDepartment of Internal Medicine and Cardiology, Osaka City University Graduate School of Medicine, 1-4-3 Asahi-machi, Abeno-ku, Osaka 545-8585, JapanDepartment of Pharmacology, Osaka City University Graduate School of Medicine, 1-4-3 Asahi-machi, Abeno-ku, Osaka 545-8585, JapanDepartment of Internal Medicine and Cardiology, Osaka City University Graduate School of Medicine, 1-4-3 Asahi-machi, Abeno-ku, Osaka 545-8585, JapanDepartment of Internal Medicine and Cardiology, Osaka City University Graduate School of Medicine, 1-4-3 Asahi-machi, Abeno-ku, Osaka 545-8585, JapanDepartment of Pharmacology, Osaka City University Graduate School of Medicine, 1-4-3 Asahi-machi, Abeno-ku, Osaka 545-8585, JapanDepartment of Internal Medicine and Cardiology, Osaka City University Graduate School of Medicine, 1-4-3 Asahi-machi, Abeno-ku, Osaka 545-8585, JapanOsteopontin has been reported to have an important role in cardiac fibrosis. However, little is known about the effects of angiotensin-converting enzyme inhibitor (ACEI) and angiotensin type 1 receptor blockers (ARB) on osteopontin expression in infarcted myocardium. The purpose of this study was to elucidate the effects of an ACEI (perindpril) and an ARB (candesartan cilexitil) on cardiac function as assessed by Doppler echocardiography and cardiac osteopontin expression associated with cardiac remodeling in myocardial infarcted rats. ACEI or ARB was administered after myocardial infarction (MI). At 4 weeks after MI, cardiac function, and mRNAs in non-infarcted myocardium were analyzed. ACEI and ARB equally prevented left ventricular dilatation, reduction of ejection fraction, and the increase in E/A wave velocity ratio and the rate of E wave deceleration by MI. ACEI and ARB significantly suppressed increased mRNA expression of atrial natriuretic peptide, brain natriuretic peptide, osteopontin, and collagen I and III in the non-infarcted ventricle at 4 weeks. Immunohistochemically stained osteopontin was increased in interstitial fibrosis of non-infarcted myocardium. Both ACEI and ARB significantly prevented cardiac fibrosis and osteopontin expression. In conclusion, angiotensin blockade inhibits osteopontin expression in non-infarcted myocardium and prevents cardiac remodeling after MI. Keywords:: osteopontin, renin-angiotensin system, cardiac remodeling, myocardial infarctionhttp://www.sciencedirect.com/science/article/pii/S1347861319321814
collection DOAJ
language English
format Article
sources DOAJ
author Takanori Kusuyama
Minoru Yoshiyama
Takashi Omura
Daisuke Nishiya
Soichiro Enomoto
Ryo Matsumoto
Yasukatsu Izumi
Kaname Akioka
Kazuhide Takeuchi
Hiroshi Iwao
Junichi Yoshikawa
spellingShingle Takanori Kusuyama
Minoru Yoshiyama
Takashi Omura
Daisuke Nishiya
Soichiro Enomoto
Ryo Matsumoto
Yasukatsu Izumi
Kaname Akioka
Kazuhide Takeuchi
Hiroshi Iwao
Junichi Yoshikawa
Angiotensin Blockade Inhibits Osteopontin Expression in Non-infarcted Myocardium After Myocardial Infarction
Journal of Pharmacological Sciences
author_facet Takanori Kusuyama
Minoru Yoshiyama
Takashi Omura
Daisuke Nishiya
Soichiro Enomoto
Ryo Matsumoto
Yasukatsu Izumi
Kaname Akioka
Kazuhide Takeuchi
Hiroshi Iwao
Junichi Yoshikawa
author_sort Takanori Kusuyama
title Angiotensin Blockade Inhibits Osteopontin Expression in Non-infarcted Myocardium After Myocardial Infarction
title_short Angiotensin Blockade Inhibits Osteopontin Expression in Non-infarcted Myocardium After Myocardial Infarction
title_full Angiotensin Blockade Inhibits Osteopontin Expression in Non-infarcted Myocardium After Myocardial Infarction
title_fullStr Angiotensin Blockade Inhibits Osteopontin Expression in Non-infarcted Myocardium After Myocardial Infarction
title_full_unstemmed Angiotensin Blockade Inhibits Osteopontin Expression in Non-infarcted Myocardium After Myocardial Infarction
title_sort angiotensin blockade inhibits osteopontin expression in non-infarcted myocardium after myocardial infarction
publisher Elsevier
series Journal of Pharmacological Sciences
issn 1347-8613
publishDate 2005-01-01
description Osteopontin has been reported to have an important role in cardiac fibrosis. However, little is known about the effects of angiotensin-converting enzyme inhibitor (ACEI) and angiotensin type 1 receptor blockers (ARB) on osteopontin expression in infarcted myocardium. The purpose of this study was to elucidate the effects of an ACEI (perindpril) and an ARB (candesartan cilexitil) on cardiac function as assessed by Doppler echocardiography and cardiac osteopontin expression associated with cardiac remodeling in myocardial infarcted rats. ACEI or ARB was administered after myocardial infarction (MI). At 4 weeks after MI, cardiac function, and mRNAs in non-infarcted myocardium were analyzed. ACEI and ARB equally prevented left ventricular dilatation, reduction of ejection fraction, and the increase in E/A wave velocity ratio and the rate of E wave deceleration by MI. ACEI and ARB significantly suppressed increased mRNA expression of atrial natriuretic peptide, brain natriuretic peptide, osteopontin, and collagen I and III in the non-infarcted ventricle at 4 weeks. Immunohistochemically stained osteopontin was increased in interstitial fibrosis of non-infarcted myocardium. Both ACEI and ARB significantly prevented cardiac fibrosis and osteopontin expression. In conclusion, angiotensin blockade inhibits osteopontin expression in non-infarcted myocardium and prevents cardiac remodeling after MI. Keywords:: osteopontin, renin-angiotensin system, cardiac remodeling, myocardial infarction
url http://www.sciencedirect.com/science/article/pii/S1347861319321814
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