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Remote Ischemic Conditioning and Stroke Recovery
Remote ischemic conditioning (RIC) is a noninvasive procedure whereby several periods of ischemia are induced in a limb. Although there is growing interest in using RIC to improve stroke recovery, preclinical RIC research has focused exclusively on neuroprotection, using male animals and the intralu...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8135236/ https://www.ncbi.nlm.nih.gov/pubmed/33955298 http://dx.doi.org/10.1177/15459683211011224 |
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author | McDonald, Matthew W. Dykes, Angela Jeffers, Matthew S. Carter, Anthony Nevins, Ralph Ripley, Allyson Silasi, Gergely Corbett, Dale |
author_facet | McDonald, Matthew W. Dykes, Angela Jeffers, Matthew S. Carter, Anthony Nevins, Ralph Ripley, Allyson Silasi, Gergely Corbett, Dale |
author_sort | McDonald, Matthew W. |
collection | PubMed |
description | Remote ischemic conditioning (RIC) is a noninvasive procedure whereby several periods of ischemia are induced in a limb. Although there is growing interest in using RIC to improve stroke recovery, preclinical RIC research has focused exclusively on neuroprotection, using male animals and the intraluminal suture stroke model, and delivered RIC at times not relevant to either brain repair or behavioral recovery. In alignment with the Stroke Recovery and Rehabilitation Roundtable, we address these shortcomings. First, a standardized session (5-minute inflation/deflation, 4 repetitions) of RIC was delivered using a cuff on the contralesional hindlimb in both male and female Sprague-Dawley rats. Using the endothelin-1 stroke model, RIC was delivered once either prestroke (18 hours before, pre-RIC) or poststroke (4 hours after, post-RIC), and infarct volume was assessed at 24 hours poststroke using magnetic resonance imaging. RIC was delivered at these times to mimic the day before a surgery where clots are possible or as a treatment similar to tissue plasminogen activator, respectively. Pre-RIC reduced infarct volume by 41% compared with 29% with post-RIC. RIC was neuroprotective in both sexes, but males had a 46% reduction of infarct volume compared with 23% in females. After confirming the acute efficacy of RIC, we applied it chronically for 4 weeks, beginning 5 days poststroke. This delayed RIC failed to enhance poststroke behavioral recovery. Based on these findings, the most promising application of RIC is during the hyperacute and early acute phases of stroke, a time when other interventions such as exercise may be contraindicated. |
format | Online Article Text |
id | pubmed-8135236 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-81352362021-06-07 Remote Ischemic Conditioning and Stroke Recovery McDonald, Matthew W. Dykes, Angela Jeffers, Matthew S. Carter, Anthony Nevins, Ralph Ripley, Allyson Silasi, Gergely Corbett, Dale Neurorehabil Neural Repair Original Research Articles Remote ischemic conditioning (RIC) is a noninvasive procedure whereby several periods of ischemia are induced in a limb. Although there is growing interest in using RIC to improve stroke recovery, preclinical RIC research has focused exclusively on neuroprotection, using male animals and the intraluminal suture stroke model, and delivered RIC at times not relevant to either brain repair or behavioral recovery. In alignment with the Stroke Recovery and Rehabilitation Roundtable, we address these shortcomings. First, a standardized session (5-minute inflation/deflation, 4 repetitions) of RIC was delivered using a cuff on the contralesional hindlimb in both male and female Sprague-Dawley rats. Using the endothelin-1 stroke model, RIC was delivered once either prestroke (18 hours before, pre-RIC) or poststroke (4 hours after, post-RIC), and infarct volume was assessed at 24 hours poststroke using magnetic resonance imaging. RIC was delivered at these times to mimic the day before a surgery where clots are possible or as a treatment similar to tissue plasminogen activator, respectively. Pre-RIC reduced infarct volume by 41% compared with 29% with post-RIC. RIC was neuroprotective in both sexes, but males had a 46% reduction of infarct volume compared with 23% in females. After confirming the acute efficacy of RIC, we applied it chronically for 4 weeks, beginning 5 days poststroke. This delayed RIC failed to enhance poststroke behavioral recovery. Based on these findings, the most promising application of RIC is during the hyperacute and early acute phases of stroke, a time when other interventions such as exercise may be contraindicated. SAGE Publications 2021-05-06 2021-06 /pmc/articles/PMC8135236/ /pubmed/33955298 http://dx.doi.org/10.1177/15459683211011224 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) 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 pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Original Research Articles McDonald, Matthew W. Dykes, Angela Jeffers, Matthew S. Carter, Anthony Nevins, Ralph Ripley, Allyson Silasi, Gergely Corbett, Dale Remote Ischemic Conditioning and Stroke Recovery |
title | Remote Ischemic Conditioning and Stroke Recovery |
title_full | Remote Ischemic Conditioning and Stroke Recovery |
title_fullStr | Remote Ischemic Conditioning and Stroke Recovery |
title_full_unstemmed | Remote Ischemic Conditioning and Stroke Recovery |
title_short | Remote Ischemic Conditioning and Stroke Recovery |
title_sort | remote ischemic conditioning and stroke recovery |
topic | Original Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8135236/ https://www.ncbi.nlm.nih.gov/pubmed/33955298 http://dx.doi.org/10.1177/15459683211011224 |
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