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Hyperglycemia aggravates decreases of PEA-15 and its two phosphorylated forms in cerebral ischemia
Diabetes is a metabolic health disorder and an important risk factor for stroke. Phosphoprotein enriched in astrocytes 15 (PEA-15) is a multifunctional protein modulating cell proliferation, survival, apoptosis and glucose metabolism. This study investigated whether diabetes modulates the expression...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Japanese Society of Veterinary Science
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5383193/ https://www.ncbi.nlm.nih.gov/pubmed/28216548 http://dx.doi.org/10.1292/jvms.16-0437 |
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author | SUNG, Jin-Hee KOH, Phil-Ok |
author_facet | SUNG, Jin-Hee KOH, Phil-Ok |
author_sort | SUNG, Jin-Hee |
collection | PubMed |
description | Diabetes is a metabolic health disorder and an important risk factor for stroke. Phosphoprotein enriched in astrocytes 15 (PEA-15) is a multifunctional protein modulating cell proliferation, survival, apoptosis and glucose metabolism. This study investigated whether diabetes modulates the expression of PEA-15 and two phosphorylated forms (Ser 104 and Ser 116) in middle cerebral artery occlusion (MCAO)-induced brain injury. Male Sprague-Dawley rats were administrated with streptozotocin (40 mg/kg) and were underwent right middle cerebral artery occlusion (MCAO) 4 weeks after streptozotocin injection. Brain tissues were collected 24 hr after MCAO and stained using triphenyltetrazolium chloride. Western blot analysis was performed to elucidate the expression of PEA-15 and two phosphorylated forms (Ser 104 and Ser 116) in right cerebral cortex. Infarct volume during MCAO injury was severely increased in diabetic animals compared to non-diabetic animals. We identified the decrease in PEA-15 in animals that underwent MCAO using proteomic approach. PEA-15 expression during MCAO was strongly decreased in diabetic animals compared to non-diabetic animals. Western blots analysis confirmed that diabetes exacerbated the decrease in PEA-15 expression after MCAO. Moreover, decrease in expression of phospho-PEA-15 (Ser 104 and Ser 116) was greater in diabetic than in non-diabetic animals. These results suggested that a diabetic condition may aggravate brain damage through decreasing expression of PEA-15 and phospho-PEA-15 (Ser 104 and Ser 116) in ischemic brain injury. |
format | Online Article Text |
id | pubmed-5383193 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | The Japanese Society of Veterinary Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-53831932017-04-11 Hyperglycemia aggravates decreases of PEA-15 and its two phosphorylated forms in cerebral ischemia SUNG, Jin-Hee KOH, Phil-Ok J Vet Med Sci Laboratory Animal Science Diabetes is a metabolic health disorder and an important risk factor for stroke. Phosphoprotein enriched in astrocytes 15 (PEA-15) is a multifunctional protein modulating cell proliferation, survival, apoptosis and glucose metabolism. This study investigated whether diabetes modulates the expression of PEA-15 and two phosphorylated forms (Ser 104 and Ser 116) in middle cerebral artery occlusion (MCAO)-induced brain injury. Male Sprague-Dawley rats were administrated with streptozotocin (40 mg/kg) and were underwent right middle cerebral artery occlusion (MCAO) 4 weeks after streptozotocin injection. Brain tissues were collected 24 hr after MCAO and stained using triphenyltetrazolium chloride. Western blot analysis was performed to elucidate the expression of PEA-15 and two phosphorylated forms (Ser 104 and Ser 116) in right cerebral cortex. Infarct volume during MCAO injury was severely increased in diabetic animals compared to non-diabetic animals. We identified the decrease in PEA-15 in animals that underwent MCAO using proteomic approach. PEA-15 expression during MCAO was strongly decreased in diabetic animals compared to non-diabetic animals. Western blots analysis confirmed that diabetes exacerbated the decrease in PEA-15 expression after MCAO. Moreover, decrease in expression of phospho-PEA-15 (Ser 104 and Ser 116) was greater in diabetic than in non-diabetic animals. These results suggested that a diabetic condition may aggravate brain damage through decreasing expression of PEA-15 and phospho-PEA-15 (Ser 104 and Ser 116) in ischemic brain injury. The Japanese Society of Veterinary Science 2017-02-17 2017-03 /pmc/articles/PMC5383193/ /pubmed/28216548 http://dx.doi.org/10.1292/jvms.16-0437 Text en ©2017 The Japanese Society of Veterinary Science This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives (by-nc-nd) License. (CC-BY-NC-ND 4.0: https://creativecommons.org/licenses/by-nc-nd/4.0/) |
spellingShingle | Laboratory Animal Science SUNG, Jin-Hee KOH, Phil-Ok Hyperglycemia aggravates decreases of PEA-15 and its two phosphorylated forms in cerebral ischemia |
title | Hyperglycemia aggravates decreases of PEA-15 and its two phosphorylated forms in cerebral ischemia |
title_full | Hyperglycemia aggravates decreases of PEA-15 and its two phosphorylated forms in cerebral ischemia |
title_fullStr | Hyperglycemia aggravates decreases of PEA-15 and its two phosphorylated forms in cerebral ischemia |
title_full_unstemmed | Hyperglycemia aggravates decreases of PEA-15 and its two phosphorylated forms in cerebral ischemia |
title_short | Hyperglycemia aggravates decreases of PEA-15 and its two phosphorylated forms in cerebral ischemia |
title_sort | hyperglycemia aggravates decreases of pea-15 and its two phosphorylated forms in cerebral ischemia |
topic | Laboratory Animal Science |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5383193/ https://www.ncbi.nlm.nih.gov/pubmed/28216548 http://dx.doi.org/10.1292/jvms.16-0437 |
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