author_facet Zhang, X.
Dostal, D. E.
Reiss, K.
Cheng, W.
Kajstura, J.
Li, P.
Huang, H.
Sonnenblick, E. H.
Meggs, L. G.
Baker, K. M.
et, al.
Zhang, X.
Dostal, D. E.
Reiss, K.
Cheng, W.
Kajstura, J.
Li, P.
Huang, H.
Sonnenblick, E. H.
Meggs, L. G.
Baker, K. M.
et, al.
author Zhang, X.
Dostal, D. E.
Reiss, K.
Cheng, W.
Kajstura, J.
Li, P.
Huang, H.
Sonnenblick, E. H.
Meggs, L. G.
Baker, K. M.
et, al.
spellingShingle Zhang, X.
Dostal, D. E.
Reiss, K.
Cheng, W.
Kajstura, J.
Li, P.
Huang, H.
Sonnenblick, E. H.
Meggs, L. G.
Baker, K. M.
et, al.
American Journal of Physiology-Heart and Circulatory Physiology
Identification and activation of autocrine renin-angiotensin system in adult ventricular myocytes
Physiology (medical)
Cardiology and Cardiovascular Medicine
Physiology
author_sort zhang, x.
spelling Zhang, X. Dostal, D. E. Reiss, K. Cheng, W. Kajstura, J. Li, P. Huang, H. Sonnenblick, E. H. Meggs, L. G. Baker, K. M. et, al. 0363-6135 1522-1539 American Physiological Society Physiology (medical) Cardiology and Cardiovascular Medicine Physiology http://dx.doi.org/10.1152/ajpheart.1995.269.5.h1791 <jats:p> To date, the demonstration that the molecular components of the renin-angiotensin system (RAS) are present in adult ventricular myocytes is lacking. In addition, whether the RAS is upregulated under conditions of overload and myocyte hypertrophy in vivo remains to be determined. By employing an in vivo model of ischemic cardiomyopathy in rats, we document that adult myocytes express genes for renin, angiotensinogen, angiotensin-converting enzyme (ACE), and angiotensin II (ANG II) receptors. Moreover, renin, ACE, and ANG II receptor mRNAs increased in stressed myocytes undergoing cellular hypertrophy. At the protein level, the percentage of myocytes containing renin, ANG I, and ANG II was significantly increased in the overloaded heart. The number of binding sites for ANG II per myocyte also markedly increased under this setting. These results provide direct evidence of the existence of a myocyte RAS, which may be activated in pathological states of the heart to support myocyte growth and contractile function. </jats:p> Identification and activation of autocrine renin-angiotensin system in adult ventricular myocytes American Journal of Physiology-Heart and Circulatory Physiology
doi_str_mv 10.1152/ajpheart.1995.269.5.h1791
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series American Journal of Physiology-Heart and Circulatory Physiology
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title Identification and activation of autocrine renin-angiotensin system in adult ventricular myocytes
title_unstemmed Identification and activation of autocrine renin-angiotensin system in adult ventricular myocytes
title_full Identification and activation of autocrine renin-angiotensin system in adult ventricular myocytes
title_fullStr Identification and activation of autocrine renin-angiotensin system in adult ventricular myocytes
title_full_unstemmed Identification and activation of autocrine renin-angiotensin system in adult ventricular myocytes
title_short Identification and activation of autocrine renin-angiotensin system in adult ventricular myocytes
title_sort identification and activation of autocrine renin-angiotensin system in adult ventricular myocytes
topic Physiology (medical)
Cardiology and Cardiovascular Medicine
Physiology
url http://dx.doi.org/10.1152/ajpheart.1995.269.5.h1791
publishDate 1995
physical H1791-H1802
description <jats:p> To date, the demonstration that the molecular components of the renin-angiotensin system (RAS) are present in adult ventricular myocytes is lacking. In addition, whether the RAS is upregulated under conditions of overload and myocyte hypertrophy in vivo remains to be determined. By employing an in vivo model of ischemic cardiomyopathy in rats, we document that adult myocytes express genes for renin, angiotensinogen, angiotensin-converting enzyme (ACE), and angiotensin II (ANG II) receptors. Moreover, renin, ACE, and ANG II receptor mRNAs increased in stressed myocytes undergoing cellular hypertrophy. At the protein level, the percentage of myocytes containing renin, ANG I, and ANG II was significantly increased in the overloaded heart. The number of binding sites for ANG II per myocyte also markedly increased under this setting. These results provide direct evidence of the existence of a myocyte RAS, which may be activated in pathological states of the heart to support myocyte growth and contractile function. </jats:p>
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author Zhang, X., Dostal, D. E., Reiss, K., Cheng, W., Kajstura, J., Li, P., Huang, H., Sonnenblick, E. H., Meggs, L. G., Baker, K. M., et, al.
author_facet Zhang, X., Dostal, D. E., Reiss, K., Cheng, W., Kajstura, J., Li, P., Huang, H., Sonnenblick, E. H., Meggs, L. G., Baker, K. M., et, al., Zhang, X., Dostal, D. E., Reiss, K., Cheng, W., Kajstura, J., Li, P., Huang, H., Sonnenblick, E. H., Meggs, L. G., Baker, K. M., et, al.
author_sort zhang, x.
container_issue 5
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container_title American Journal of Physiology-Heart and Circulatory Physiology
container_volume 269
description <jats:p> To date, the demonstration that the molecular components of the renin-angiotensin system (RAS) are present in adult ventricular myocytes is lacking. In addition, whether the RAS is upregulated under conditions of overload and myocyte hypertrophy in vivo remains to be determined. By employing an in vivo model of ischemic cardiomyopathy in rats, we document that adult myocytes express genes for renin, angiotensinogen, angiotensin-converting enzyme (ACE), and angiotensin II (ANG II) receptors. Moreover, renin, ACE, and ANG II receptor mRNAs increased in stressed myocytes undergoing cellular hypertrophy. At the protein level, the percentage of myocytes containing renin, ANG I, and ANG II was significantly increased in the overloaded heart. The number of binding sites for ANG II per myocyte also markedly increased under this setting. These results provide direct evidence of the existence of a myocyte RAS, which may be activated in pathological states of the heart to support myocyte growth and contractile function. </jats:p>
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spelling Zhang, X. Dostal, D. E. Reiss, K. Cheng, W. Kajstura, J. Li, P. Huang, H. Sonnenblick, E. H. Meggs, L. G. Baker, K. M. et, al. 0363-6135 1522-1539 American Physiological Society Physiology (medical) Cardiology and Cardiovascular Medicine Physiology http://dx.doi.org/10.1152/ajpheart.1995.269.5.h1791 <jats:p> To date, the demonstration that the molecular components of the renin-angiotensin system (RAS) are present in adult ventricular myocytes is lacking. In addition, whether the RAS is upregulated under conditions of overload and myocyte hypertrophy in vivo remains to be determined. By employing an in vivo model of ischemic cardiomyopathy in rats, we document that adult myocytes express genes for renin, angiotensinogen, angiotensin-converting enzyme (ACE), and angiotensin II (ANG II) receptors. Moreover, renin, ACE, and ANG II receptor mRNAs increased in stressed myocytes undergoing cellular hypertrophy. At the protein level, the percentage of myocytes containing renin, ANG I, and ANG II was significantly increased in the overloaded heart. The number of binding sites for ANG II per myocyte also markedly increased under this setting. These results provide direct evidence of the existence of a myocyte RAS, which may be activated in pathological states of the heart to support myocyte growth and contractile function. </jats:p> Identification and activation of autocrine renin-angiotensin system in adult ventricular myocytes American Journal of Physiology-Heart and Circulatory Physiology
spellingShingle Zhang, X., Dostal, D. E., Reiss, K., Cheng, W., Kajstura, J., Li, P., Huang, H., Sonnenblick, E. H., Meggs, L. G., Baker, K. M., et, al., American Journal of Physiology-Heart and Circulatory Physiology, Identification and activation of autocrine renin-angiotensin system in adult ventricular myocytes, Physiology (medical), Cardiology and Cardiovascular Medicine, Physiology
title Identification and activation of autocrine renin-angiotensin system in adult ventricular myocytes
title_full Identification and activation of autocrine renin-angiotensin system in adult ventricular myocytes
title_fullStr Identification and activation of autocrine renin-angiotensin system in adult ventricular myocytes
title_full_unstemmed Identification and activation of autocrine renin-angiotensin system in adult ventricular myocytes
title_short Identification and activation of autocrine renin-angiotensin system in adult ventricular myocytes
title_sort identification and activation of autocrine renin-angiotensin system in adult ventricular myocytes
title_unstemmed Identification and activation of autocrine renin-angiotensin system in adult ventricular myocytes
topic Physiology (medical), Cardiology and Cardiovascular Medicine, Physiology
url http://dx.doi.org/10.1152/ajpheart.1995.269.5.h1791