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Remote Ischemic Postconditioning: Harnessing Endogenous Protection in a Murine Model of Vascular Cognitive Impairment

We previously reported that remote limb ischemic conditioning (RLIC; PERconditioning) during acute stroke confers neuroprotection, possibly due to increased cerebral blood flow (CBF). Vascular cognitive impairment (VCI) is a growing threat to public health without any known treatment. The bilateral...

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Autores principales: Khan, Mohammad Badruzzaman, Hoda, Md Nasrul, Vaibhav, Kumar, Giri, Shailendra, Wang, Philip, Waller, Jennifer L., Ergul, Adviye, Dhandapani, Krishnan M., Fagan, Susan C., Hess, David C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4297613/
https://www.ncbi.nlm.nih.gov/pubmed/25351177
http://dx.doi.org/10.1007/s12975-014-0374-6
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author Khan, Mohammad Badruzzaman
Hoda, Md Nasrul
Vaibhav, Kumar
Giri, Shailendra
Wang, Philip
Waller, Jennifer L.
Ergul, Adviye
Dhandapani, Krishnan M.
Fagan, Susan C.
Hess, David C.
author_facet Khan, Mohammad Badruzzaman
Hoda, Md Nasrul
Vaibhav, Kumar
Giri, Shailendra
Wang, Philip
Waller, Jennifer L.
Ergul, Adviye
Dhandapani, Krishnan M.
Fagan, Susan C.
Hess, David C.
author_sort Khan, Mohammad Badruzzaman
collection PubMed
description We previously reported that remote limb ischemic conditioning (RLIC; PERconditioning) during acute stroke confers neuroprotection, possibly due to increased cerebral blood flow (CBF). Vascular cognitive impairment (VCI) is a growing threat to public health without any known treatment. The bilateral common carotid artery stenosis (BCAS) mouse model is regarded as the most valid model for VCI. We hypothesized that RLIC (postconditioning; RIPostC) will augment CBF during chronic cerebral hypoperfusion (CCH) and prevent cognitive impairment in the BCAS model. BCAS using customized microcoil was performed in C57/B6 male mice to establish CCH. A week after the BCAS surgery, mice were treated with RIPostC-therapy once daily for 2 weeks. CBF was measured with laser speckle contrast imager at different time points. Cognitive testing was performed at 4-week post-BCAS, and brain tissue was harvested for biochemistry. BCAS led to chronic hypoperfusion resulting into impaired cognitive function as tested by novel object recognition (NOR). Histological examinations revealed that BCAS triggered inflammatory responses and caused frequent vacuolization and cell death. BCAS also increased the generation and accumulation of amyloid beta protein (Aβ), resulting into the loss of white matter (WM) and myelin basic protein (MBP). RIPostC-therapy showed both acute increase as well as sustained improvement in CBF even after the cessation of therapy for a week. RIPostC improved cognitive function, inhibited inflammatory responses, prevented the cell death, reduced the generation and accumulation of Aβ, and protected WM integrity. RIPostC is effective in the BCAS model and could be an attractive low-cost conventional therapy for aged individuals with VCI. The mechanisms by which RIPostC improves CBF and attenuates tissue damage need to be investigated in the future. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s12975-014-0374-6) contains supplementary material, which is available to authorized users.
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spelling pubmed-42976132015-01-21 Remote Ischemic Postconditioning: Harnessing Endogenous Protection in a Murine Model of Vascular Cognitive Impairment Khan, Mohammad Badruzzaman Hoda, Md Nasrul Vaibhav, Kumar Giri, Shailendra Wang, Philip Waller, Jennifer L. Ergul, Adviye Dhandapani, Krishnan M. Fagan, Susan C. Hess, David C. Transl Stroke Res Original Article We previously reported that remote limb ischemic conditioning (RLIC; PERconditioning) during acute stroke confers neuroprotection, possibly due to increased cerebral blood flow (CBF). Vascular cognitive impairment (VCI) is a growing threat to public health without any known treatment. The bilateral common carotid artery stenosis (BCAS) mouse model is regarded as the most valid model for VCI. We hypothesized that RLIC (postconditioning; RIPostC) will augment CBF during chronic cerebral hypoperfusion (CCH) and prevent cognitive impairment in the BCAS model. BCAS using customized microcoil was performed in C57/B6 male mice to establish CCH. A week after the BCAS surgery, mice were treated with RIPostC-therapy once daily for 2 weeks. CBF was measured with laser speckle contrast imager at different time points. Cognitive testing was performed at 4-week post-BCAS, and brain tissue was harvested for biochemistry. BCAS led to chronic hypoperfusion resulting into impaired cognitive function as tested by novel object recognition (NOR). Histological examinations revealed that BCAS triggered inflammatory responses and caused frequent vacuolization and cell death. BCAS also increased the generation and accumulation of amyloid beta protein (Aβ), resulting into the loss of white matter (WM) and myelin basic protein (MBP). RIPostC-therapy showed both acute increase as well as sustained improvement in CBF even after the cessation of therapy for a week. RIPostC improved cognitive function, inhibited inflammatory responses, prevented the cell death, reduced the generation and accumulation of Aβ, and protected WM integrity. RIPostC is effective in the BCAS model and could be an attractive low-cost conventional therapy for aged individuals with VCI. The mechanisms by which RIPostC improves CBF and attenuates tissue damage need to be investigated in the future. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s12975-014-0374-6) contains supplementary material, which is available to authorized users. Springer US 2014-10-29 2015 /pmc/articles/PMC4297613/ /pubmed/25351177 http://dx.doi.org/10.1007/s12975-014-0374-6 Text en © The Author(s) 2014 https://creativecommons.org/licenses/by/4.0/ Open Access This article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.
spellingShingle Original Article
Khan, Mohammad Badruzzaman
Hoda, Md Nasrul
Vaibhav, Kumar
Giri, Shailendra
Wang, Philip
Waller, Jennifer L.
Ergul, Adviye
Dhandapani, Krishnan M.
Fagan, Susan C.
Hess, David C.
Remote Ischemic Postconditioning: Harnessing Endogenous Protection in a Murine Model of Vascular Cognitive Impairment
title Remote Ischemic Postconditioning: Harnessing Endogenous Protection in a Murine Model of Vascular Cognitive Impairment
title_full Remote Ischemic Postconditioning: Harnessing Endogenous Protection in a Murine Model of Vascular Cognitive Impairment
title_fullStr Remote Ischemic Postconditioning: Harnessing Endogenous Protection in a Murine Model of Vascular Cognitive Impairment
title_full_unstemmed Remote Ischemic Postconditioning: Harnessing Endogenous Protection in a Murine Model of Vascular Cognitive Impairment
title_short Remote Ischemic Postconditioning: Harnessing Endogenous Protection in a Murine Model of Vascular Cognitive Impairment
title_sort remote ischemic postconditioning: harnessing endogenous protection in a murine model of vascular cognitive impairment
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4297613/
https://www.ncbi.nlm.nih.gov/pubmed/25351177
http://dx.doi.org/10.1007/s12975-014-0374-6
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