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Neuroprotective Effects of Liraglutide for Stroke Model of Rats
The number of diabetes mellitus (DM) patients is increasing, and stroke is deeply associated with DM. Recently, neuroprotective effects of glucagon-like peptide-1 (GLP-1) are reported. In this study, we explored whether liraglutide, a GLP-1 analogue exerts therapeutic effects on a rat stroke model....
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Molecular Diversity Preservation International (MDPI)
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3856019/ https://www.ncbi.nlm.nih.gov/pubmed/24177570 http://dx.doi.org/10.3390/ijms141121513 |
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author | Sato, Kenichiro Kameda, Masahiro Yasuhara, Takao Agari, Takashi Baba, Tanefumi Wang, Feifei Shinko, Aiko Wakamori, Takaaki Toyoshima, Atsuhiko Takeuchi, Hayato Sasaki, Tatsuya Sasada, Susumu Kondo, Akihiko Borlongan, Cesario V. Matsumae, Mitsunori Date, Isao |
author_facet | Sato, Kenichiro Kameda, Masahiro Yasuhara, Takao Agari, Takashi Baba, Tanefumi Wang, Feifei Shinko, Aiko Wakamori, Takaaki Toyoshima, Atsuhiko Takeuchi, Hayato Sasaki, Tatsuya Sasada, Susumu Kondo, Akihiko Borlongan, Cesario V. Matsumae, Mitsunori Date, Isao |
author_sort | Sato, Kenichiro |
collection | PubMed |
description | The number of diabetes mellitus (DM) patients is increasing, and stroke is deeply associated with DM. Recently, neuroprotective effects of glucagon-like peptide-1 (GLP-1) are reported. In this study, we explored whether liraglutide, a GLP-1 analogue exerts therapeutic effects on a rat stroke model. Wistar rats received occlusion of the middle cerebral artery for 90 min. At one hour after reperfusion, liraglutide or saline was administered intraperitoneally. Modified Bederson’s test was performed at 1 and 24 h and, subsequently, rats were euthanized for histological investigation. Peripheral blood was obtained for measurement of blood glucose level and evaluation of oxidative stress. Brain tissues were collected to evaluate the level of vascular endothelial growth factor (VEGF). The behavioral scores of liraglutide-treated rats were significantly better than those of control rats. Infarct volumes of liraglutide-treated rats at were reduced, compared with those of control rats. The level of derivatives of reactive oxygen metabolite was lower in liraglutide-treated rats. VEGF level of liraglutide-treated rats in the cortex, but not in the striatum significantly increased, compared to that of control rats. In conclusion, this is the first study to demonstrate neuroprotective effects of liraglutide on cerebral ischemia through anti-oxidative effects and VEGF upregulation. |
format | Online Article Text |
id | pubmed-3856019 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Molecular Diversity Preservation International (MDPI) |
record_format | MEDLINE/PubMed |
spelling | pubmed-38560192013-12-09 Neuroprotective Effects of Liraglutide for Stroke Model of Rats Sato, Kenichiro Kameda, Masahiro Yasuhara, Takao Agari, Takashi Baba, Tanefumi Wang, Feifei Shinko, Aiko Wakamori, Takaaki Toyoshima, Atsuhiko Takeuchi, Hayato Sasaki, Tatsuya Sasada, Susumu Kondo, Akihiko Borlongan, Cesario V. Matsumae, Mitsunori Date, Isao Int J Mol Sci Article The number of diabetes mellitus (DM) patients is increasing, and stroke is deeply associated with DM. Recently, neuroprotective effects of glucagon-like peptide-1 (GLP-1) are reported. In this study, we explored whether liraglutide, a GLP-1 analogue exerts therapeutic effects on a rat stroke model. Wistar rats received occlusion of the middle cerebral artery for 90 min. At one hour after reperfusion, liraglutide or saline was administered intraperitoneally. Modified Bederson’s test was performed at 1 and 24 h and, subsequently, rats were euthanized for histological investigation. Peripheral blood was obtained for measurement of blood glucose level and evaluation of oxidative stress. Brain tissues were collected to evaluate the level of vascular endothelial growth factor (VEGF). The behavioral scores of liraglutide-treated rats were significantly better than those of control rats. Infarct volumes of liraglutide-treated rats at were reduced, compared with those of control rats. The level of derivatives of reactive oxygen metabolite was lower in liraglutide-treated rats. VEGF level of liraglutide-treated rats in the cortex, but not in the striatum significantly increased, compared to that of control rats. In conclusion, this is the first study to demonstrate neuroprotective effects of liraglutide on cerebral ischemia through anti-oxidative effects and VEGF upregulation. Molecular Diversity Preservation International (MDPI) 2013-10-30 /pmc/articles/PMC3856019/ /pubmed/24177570 http://dx.doi.org/10.3390/ijms141121513 Text en © 2013 by the authors; licensee MDPI, Basel, Switzerland http://creativecommons.org/licenses/by/3.0/ This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/). |
spellingShingle | Article Sato, Kenichiro Kameda, Masahiro Yasuhara, Takao Agari, Takashi Baba, Tanefumi Wang, Feifei Shinko, Aiko Wakamori, Takaaki Toyoshima, Atsuhiko Takeuchi, Hayato Sasaki, Tatsuya Sasada, Susumu Kondo, Akihiko Borlongan, Cesario V. Matsumae, Mitsunori Date, Isao Neuroprotective Effects of Liraglutide for Stroke Model of Rats |
title | Neuroprotective Effects of Liraglutide for Stroke Model of Rats |
title_full | Neuroprotective Effects of Liraglutide for Stroke Model of Rats |
title_fullStr | Neuroprotective Effects of Liraglutide for Stroke Model of Rats |
title_full_unstemmed | Neuroprotective Effects of Liraglutide for Stroke Model of Rats |
title_short | Neuroprotective Effects of Liraglutide for Stroke Model of Rats |
title_sort | neuroprotective effects of liraglutide for stroke model of rats |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3856019/ https://www.ncbi.nlm.nih.gov/pubmed/24177570 http://dx.doi.org/10.3390/ijms141121513 |
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