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Lipid Emulsion Improves Functional Recovery in an Animal Model of Stroke

Stroke is a life-threatening condition that leads to the death of many people around the world. Reperfusion injury after ischemic stroke is a recurrent problem associated with various surgical procedures that involve the removal of blockages in the brain arteries. Lipid emulsion was recently shown t...

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Autores principales: Tanioka, Motomasa, Park, Wyun Kon, Park, Joohyun, Lee, Jong Eun, Lee, Bae Hwan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7582956/
https://www.ncbi.nlm.nih.gov/pubmed/33036206
http://dx.doi.org/10.3390/ijms21197373
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author Tanioka, Motomasa
Park, Wyun Kon
Park, Joohyun
Lee, Jong Eun
Lee, Bae Hwan
author_facet Tanioka, Motomasa
Park, Wyun Kon
Park, Joohyun
Lee, Jong Eun
Lee, Bae Hwan
author_sort Tanioka, Motomasa
collection PubMed
description Stroke is a life-threatening condition that leads to the death of many people around the world. Reperfusion injury after ischemic stroke is a recurrent problem associated with various surgical procedures that involve the removal of blockages in the brain arteries. Lipid emulsion was recently shown to attenuate ischemic reperfusion injury in the heart and to protect the brain from excitotoxicity. However, investigations on the protective mechanisms of lipid emulsion against ischemia in the brain are still lacking. This study aimed to determine the neuroprotective effects of lipid emulsion in an in vivo rat model of ischemic reperfusion injury through middle cerebral artery occlusion (MCAO). Under sodium pentobarbital anesthesia, rats were subjected to MCAO surgery and were administered with lipid emulsion through intra-arterial injection during reperfusion. The experimental animals were assessed for neurological deficit wherein the brains were extracted at 24 h after reperfusion for triphenyltetrazolium chloride staining, immunoblotting and qPCR. Neuroprotection was found to be dosage-dependent and the rats treated with 20% lipid emulsion had significantly decreased infarction volumes and lower Bederson scores. Phosphorylation of Akt and glycogen synthase kinase 3-β (GSK3-β) were increased in the 20% lipid-emulsion treated group. The Wnt-associated signals showed a marked increase with a concomitant decrease in signals of inflammatory markers in the group treated with 20% lipid emulsion. The protective effects of lipid emulsion and survival-related expression of genes such as Akt, GSK-3β, Wnt1 and β-catenin were reversed by the intra-peritoneal administration of XAV939 through the inhibition of the Wnt/β-catenin signaling pathway. These results suggest that lipid emulsion has neuroprotective effects against ischemic reperfusion injury in the brain through the modulation of the Wnt signaling pathway and may provide potential insights for the development of therapeutic targets.
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spelling pubmed-75829562020-10-28 Lipid Emulsion Improves Functional Recovery in an Animal Model of Stroke Tanioka, Motomasa Park, Wyun Kon Park, Joohyun Lee, Jong Eun Lee, Bae Hwan Int J Mol Sci Article Stroke is a life-threatening condition that leads to the death of many people around the world. Reperfusion injury after ischemic stroke is a recurrent problem associated with various surgical procedures that involve the removal of blockages in the brain arteries. Lipid emulsion was recently shown to attenuate ischemic reperfusion injury in the heart and to protect the brain from excitotoxicity. However, investigations on the protective mechanisms of lipid emulsion against ischemia in the brain are still lacking. This study aimed to determine the neuroprotective effects of lipid emulsion in an in vivo rat model of ischemic reperfusion injury through middle cerebral artery occlusion (MCAO). Under sodium pentobarbital anesthesia, rats were subjected to MCAO surgery and were administered with lipid emulsion through intra-arterial injection during reperfusion. The experimental animals were assessed for neurological deficit wherein the brains were extracted at 24 h after reperfusion for triphenyltetrazolium chloride staining, immunoblotting and qPCR. Neuroprotection was found to be dosage-dependent and the rats treated with 20% lipid emulsion had significantly decreased infarction volumes and lower Bederson scores. Phosphorylation of Akt and glycogen synthase kinase 3-β (GSK3-β) were increased in the 20% lipid-emulsion treated group. The Wnt-associated signals showed a marked increase with a concomitant decrease in signals of inflammatory markers in the group treated with 20% lipid emulsion. The protective effects of lipid emulsion and survival-related expression of genes such as Akt, GSK-3β, Wnt1 and β-catenin were reversed by the intra-peritoneal administration of XAV939 through the inhibition of the Wnt/β-catenin signaling pathway. These results suggest that lipid emulsion has neuroprotective effects against ischemic reperfusion injury in the brain through the modulation of the Wnt signaling pathway and may provide potential insights for the development of therapeutic targets. MDPI 2020-10-06 /pmc/articles/PMC7582956/ /pubmed/33036206 http://dx.doi.org/10.3390/ijms21197373 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Tanioka, Motomasa
Park, Wyun Kon
Park, Joohyun
Lee, Jong Eun
Lee, Bae Hwan
Lipid Emulsion Improves Functional Recovery in an Animal Model of Stroke
title Lipid Emulsion Improves Functional Recovery in an Animal Model of Stroke
title_full Lipid Emulsion Improves Functional Recovery in an Animal Model of Stroke
title_fullStr Lipid Emulsion Improves Functional Recovery in an Animal Model of Stroke
title_full_unstemmed Lipid Emulsion Improves Functional Recovery in an Animal Model of Stroke
title_short Lipid Emulsion Improves Functional Recovery in an Animal Model of Stroke
title_sort lipid emulsion improves functional recovery in an animal model of stroke
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7582956/
https://www.ncbi.nlm.nih.gov/pubmed/33036206
http://dx.doi.org/10.3390/ijms21197373
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