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      Remote Ischemic Conditioning and Stroke Recovery

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          Abstract

          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.

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          Most cited references13

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          Agreed definitions and a shared vision for new standards in stroke recovery research: The Stroke Recovery and Rehabilitation Roundtable taskforce

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            Efficacy and safety of very early mobilisation within 24 h of stroke onset (AVERT): a randomised controlled trial.

            Early mobilisation after stroke is thought to contribute to the effects of stroke-unit care; however, the intervention is poorly defined and not underpinned by strong evidence. We aimed to compare the effectiveness of frequent, higher dose, very early mobilisation with usual care after stroke.
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              Rodent models of focal stroke: size, mechanism, and purpose.

              Rodent stroke models provide the experimental backbone for the in vivo determination of the mechanisms of cell death and neural repair, and for the initial testing of neuroprotective compounds. Less than 10 rodent models of focal stroke are routinely used in experimental study. These vary widely in their ability to model the human disease, and in their application to the study of cell death or neural repair. Many rodent focal stroke models produce large infarcts that more closely resemble malignant and fatal human infarction than the average sized human stroke. This review focuses on the mechanisms of ischemic damage in rat and mouse stroke models, the relative size of stroke generated in each model, and the purpose with which focal stroke models are applied to the study of ischemic cell death and to neural repair after stroke.
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                Author and article information

                Journal
                Neurorehabil Neural Repair
                Neurorehabil Neural Repair
                NNR
                spnnr
                Neurorehabilitation and Neural Repair
                SAGE Publications (Sage CA: Los Angeles, CA )
                1545-9683
                1552-6844
                6 May 2021
                June 2021
                : 35
                : 6
                : 545-549
                Affiliations
                [1 ]University of Ottawa, ON, Canada
                [2 ]Canadian Partnership for Stroke Recovery, Ottawa, ON, Canada
                Author notes
                [*]Dale Corbett, PhD, Department of Cellular & Molecular Medicine, University of Ottawa, 451 Smyth Road, Roger Guindon Hall, Ottawa, ON K1H 8M5, Canada. Email: dcorbett@ 123456uottawa.ca
                Author information
                https://orcid.org/0000-0002-0171-6102
                https://orcid.org/0000-0002-4148-2638
                https://orcid.org/0000-0003-0217-4576
                Article
                10.1177_15459683211011224
                10.1177/15459683211011224
                8135236
                33955298
                3e61ece8-3210-48cd-bbba-104745ba054d
                © The Author(s) 2021

                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).

                History
                Funding
                Funded by: Canadian Institutes of Health Research Canadian Consortium on Neurodegeneration and Aging, ;
                Funded by: Heart and Stroke Foundation Canadian Partnership for Stroke Recovery, ;
                Categories
                Original Research Articles
                Custom metadata
                ts1

                cell death,brain repair,neuroprotection
                cell death, brain repair, neuroprotection

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