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Serum activity of angiotensin converting enzyme 2 is decreased in patients with acute ischemic stroke
Levels of angiotensin converting enzyme 2 (ACE2), a cardio and neuro-protective carboxypeptidase, are dynamically altered after stroke in preclinical models. We sought to characterize the previously unexplored changes in serum ACE2 activity of stroke patients and the mechanism of these changes. Seru...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5843889/ https://www.ncbi.nlm.nih.gov/pubmed/27488276 http://dx.doi.org/10.1177/1470320316661060 |
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author | Bennion, Douglas M Rosado, Christian A Haltigan, Emily A Regenhardt, Robert W Sumners, Colin Waters, Michael F |
author_facet | Bennion, Douglas M Rosado, Christian A Haltigan, Emily A Regenhardt, Robert W Sumners, Colin Waters, Michael F |
author_sort | Bennion, Douglas M |
collection | PubMed |
description | Levels of angiotensin converting enzyme 2 (ACE2), a cardio and neuro-protective carboxypeptidase, are dynamically altered after stroke in preclinical models. We sought to characterize the previously unexplored changes in serum ACE2 activity of stroke patients and the mechanism of these changes. Serum samples were obtained from patients during acute ischemic stroke (n=39), conditions mimicking stroke (stroke-alert, n=23), or from control participants (n=20). Enzyme activity levels were analyzed by fluorometric assay and correlated with clinical variables by regression analyses. Serum ACE2 activity was significantly lower in acute ischemic stroke as compared to both control and stroke-alert patients, followed by an increase to control levels at three days. Serum ACE2 activity significantly correlated with the presence of ischemic stroke after controlling for other factors (P=0.01). Additional associations with ACE2 activity included a positive correlation with systolic blood pressure at presentation in stroke-alert (R(2)=0.24, P=0.03), while stroke levels showed no correlation (R(2)=0.01, P=0.50). ACE2 sheddase activity was unchanged between groups. These dynamic changes in serum ACE2 activity in stroke, which concur with preclinical studies, are not likely to be driven primarily by acute changes in blood pressure or sheddase activity. These findings provide new insight for developing therapies targeting this protective system in ischemic stroke. |
format | Online Article Text |
id | pubmed-5843889 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-58438892018-03-20 Serum activity of angiotensin converting enzyme 2 is decreased in patients with acute ischemic stroke Bennion, Douglas M Rosado, Christian A Haltigan, Emily A Regenhardt, Robert W Sumners, Colin Waters, Michael F J Renin Angiotensin Aldosterone Syst Original Article Levels of angiotensin converting enzyme 2 (ACE2), a cardio and neuro-protective carboxypeptidase, are dynamically altered after stroke in preclinical models. We sought to characterize the previously unexplored changes in serum ACE2 activity of stroke patients and the mechanism of these changes. Serum samples were obtained from patients during acute ischemic stroke (n=39), conditions mimicking stroke (stroke-alert, n=23), or from control participants (n=20). Enzyme activity levels were analyzed by fluorometric assay and correlated with clinical variables by regression analyses. Serum ACE2 activity was significantly lower in acute ischemic stroke as compared to both control and stroke-alert patients, followed by an increase to control levels at three days. Serum ACE2 activity significantly correlated with the presence of ischemic stroke after controlling for other factors (P=0.01). Additional associations with ACE2 activity included a positive correlation with systolic blood pressure at presentation in stroke-alert (R(2)=0.24, P=0.03), while stroke levels showed no correlation (R(2)=0.01, P=0.50). ACE2 sheddase activity was unchanged between groups. These dynamic changes in serum ACE2 activity in stroke, which concur with preclinical studies, are not likely to be driven primarily by acute changes in blood pressure or sheddase activity. These findings provide new insight for developing therapies targeting this protective system in ischemic stroke. SAGE Publications 2016-08-03 /pmc/articles/PMC5843889/ /pubmed/27488276 http://dx.doi.org/10.1177/1470320316661060 Text en © The Author(s) 2016 http://creativecommons.org/licenses/by-nc/3.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 3.0 License (http://www.creativecommons.org/licenses/by-nc/3.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access page (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Original Article Bennion, Douglas M Rosado, Christian A Haltigan, Emily A Regenhardt, Robert W Sumners, Colin Waters, Michael F Serum activity of angiotensin converting enzyme 2 is decreased in patients with acute ischemic stroke |
title | Serum activity of angiotensin converting enzyme 2 is decreased in patients with acute ischemic stroke |
title_full | Serum activity of angiotensin converting enzyme 2 is decreased in patients with acute ischemic stroke |
title_fullStr | Serum activity of angiotensin converting enzyme 2 is decreased in patients with acute ischemic stroke |
title_full_unstemmed | Serum activity of angiotensin converting enzyme 2 is decreased in patients with acute ischemic stroke |
title_short | Serum activity of angiotensin converting enzyme 2 is decreased in patients with acute ischemic stroke |
title_sort | serum activity of angiotensin converting enzyme 2 is decreased in patients with acute ischemic stroke |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5843889/ https://www.ncbi.nlm.nih.gov/pubmed/27488276 http://dx.doi.org/10.1177/1470320316661060 |
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