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RAS modulation prevents progressive cognitive impairment after experimental stroke: a randomized, blinded preclinical trial
BACKGROUND: With the aging population, the prevalence and incidence of cerebrovascular disease will continue to rise, as well as the number of individuals with vascular cognitive impairment/dementia (VCID). No specific FDA-approved treatments for VCID exist. Although clinical evidence supports that...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6090822/ https://www.ncbi.nlm.nih.gov/pubmed/30103772 http://dx.doi.org/10.1186/s12974-018-1262-x |
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author | Ahmed, Heba A. Ishrat, Tauheed Pillai, Bindu Fouda, Abdelrahman Y. Sayed, Mohammed A. Eldahshan, Wael Waller, Jennifer L. Ergul, Adviye Fagan, Susan C. |
author_facet | Ahmed, Heba A. Ishrat, Tauheed Pillai, Bindu Fouda, Abdelrahman Y. Sayed, Mohammed A. Eldahshan, Wael Waller, Jennifer L. Ergul, Adviye Fagan, Susan C. |
author_sort | Ahmed, Heba A. |
collection | PubMed |
description | BACKGROUND: With the aging population, the prevalence and incidence of cerebrovascular disease will continue to rise, as well as the number of individuals with vascular cognitive impairment/dementia (VCID). No specific FDA-approved treatments for VCID exist. Although clinical evidence supports that angiotensin receptor blockers (ARBs) prevent cognitive decline in older adults, whether ARBs have a similar effect on VCID after stroke is unknown. Moreover, these agents reduce BP, which is undesirable in the acute stroke period, so we believe that giving C21 in this acute phase or delaying ARB administration would enable us to achieve the neurovascular benefits without the risk of unintended and potentially dangerous, acute BP lowering. METHODS: The aim of our study was to determine the impact of candesartan (ARB) or compound-21 (an angiotensin type 2 receptor––AT2R––agonist) on long-term cognitive function post-stroke, in spontaneously hypertensive rats (SHRs). We hypothesized that AT2R stimulation, either directly with C21, or indirectly by blocking the angiotensin type 1 receptor (AT1R) with candesartan, initiated after stroke, would reduce cognitive impairment. Animals were subjected to a 60-min transient middle cerebral artery occlusion and randomly assigned to either saline/C21 monotherapy, for the full study duration (30 days), or given sequential therapy starting with saline/C21 (7 days) followed by candesartan for the remainder of the study (21 days). Outcome measures included sensorimotor/cognitive-function, amyloid-β determination, and histopathologic analyses. RESULTS: Treatment with RAS modulators effectively preserved cognitive function, reduced cytotoxicity, and prevented chronic-reactive microgliosis in SHRs, post-stroke. These protective effects were apparent even when treatment was delayed up to 7 days post-stroke and were independent of blood pressure and β-amyloid accumulation. CONCLUSION: Collectively, our findings demonstrate that RAS modulators effectively prevent cognitive impairment after stroke, even when treatment is delayed. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12974-018-1262-x) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6090822 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-60908222018-08-17 RAS modulation prevents progressive cognitive impairment after experimental stroke: a randomized, blinded preclinical trial Ahmed, Heba A. Ishrat, Tauheed Pillai, Bindu Fouda, Abdelrahman Y. Sayed, Mohammed A. Eldahshan, Wael Waller, Jennifer L. Ergul, Adviye Fagan, Susan C. J Neuroinflammation Research BACKGROUND: With the aging population, the prevalence and incidence of cerebrovascular disease will continue to rise, as well as the number of individuals with vascular cognitive impairment/dementia (VCID). No specific FDA-approved treatments for VCID exist. Although clinical evidence supports that angiotensin receptor blockers (ARBs) prevent cognitive decline in older adults, whether ARBs have a similar effect on VCID after stroke is unknown. Moreover, these agents reduce BP, which is undesirable in the acute stroke period, so we believe that giving C21 in this acute phase or delaying ARB administration would enable us to achieve the neurovascular benefits without the risk of unintended and potentially dangerous, acute BP lowering. METHODS: The aim of our study was to determine the impact of candesartan (ARB) or compound-21 (an angiotensin type 2 receptor––AT2R––agonist) on long-term cognitive function post-stroke, in spontaneously hypertensive rats (SHRs). We hypothesized that AT2R stimulation, either directly with C21, or indirectly by blocking the angiotensin type 1 receptor (AT1R) with candesartan, initiated after stroke, would reduce cognitive impairment. Animals were subjected to a 60-min transient middle cerebral artery occlusion and randomly assigned to either saline/C21 monotherapy, for the full study duration (30 days), or given sequential therapy starting with saline/C21 (7 days) followed by candesartan for the remainder of the study (21 days). Outcome measures included sensorimotor/cognitive-function, amyloid-β determination, and histopathologic analyses. RESULTS: Treatment with RAS modulators effectively preserved cognitive function, reduced cytotoxicity, and prevented chronic-reactive microgliosis in SHRs, post-stroke. These protective effects were apparent even when treatment was delayed up to 7 days post-stroke and were independent of blood pressure and β-amyloid accumulation. CONCLUSION: Collectively, our findings demonstrate that RAS modulators effectively prevent cognitive impairment after stroke, even when treatment is delayed. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12974-018-1262-x) contains supplementary material, which is available to authorized users. BioMed Central 2018-08-13 /pmc/articles/PMC6090822/ /pubmed/30103772 http://dx.doi.org/10.1186/s12974-018-1262-x Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Ahmed, Heba A. Ishrat, Tauheed Pillai, Bindu Fouda, Abdelrahman Y. Sayed, Mohammed A. Eldahshan, Wael Waller, Jennifer L. Ergul, Adviye Fagan, Susan C. RAS modulation prevents progressive cognitive impairment after experimental stroke: a randomized, blinded preclinical trial |
title | RAS modulation prevents progressive cognitive impairment after experimental stroke: a randomized, blinded preclinical trial |
title_full | RAS modulation prevents progressive cognitive impairment after experimental stroke: a randomized, blinded preclinical trial |
title_fullStr | RAS modulation prevents progressive cognitive impairment after experimental stroke: a randomized, blinded preclinical trial |
title_full_unstemmed | RAS modulation prevents progressive cognitive impairment after experimental stroke: a randomized, blinded preclinical trial |
title_short | RAS modulation prevents progressive cognitive impairment after experimental stroke: a randomized, blinded preclinical trial |
title_sort | ras modulation prevents progressive cognitive impairment after experimental stroke: a randomized, blinded preclinical trial |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6090822/ https://www.ncbi.nlm.nih.gov/pubmed/30103772 http://dx.doi.org/10.1186/s12974-018-1262-x |
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