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A secretory phospholipase A(2)-mediated neuroprotection and anti-apoptosis
BACKGROUND: Phospholipase A(2 )liberates free fatty acids and lysophospholipids upon hydrolysis of phospholipids and these products are often associated with detrimental effects such as inflammation and cerebral ischemia. The neuroprotective effect of neutral phospholipase from snake venom has been...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2758888/ https://www.ncbi.nlm.nih.gov/pubmed/19775433 http://dx.doi.org/10.1186/1471-2202-10-120 |
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author | Armugam, Arunmozhiarasi Cher, Charmian DN Lim, KaiYing Koh, Dawn CI Howells, David W Jeyaseelan, Kandiah |
author_facet | Armugam, Arunmozhiarasi Cher, Charmian DN Lim, KaiYing Koh, Dawn CI Howells, David W Jeyaseelan, Kandiah |
author_sort | Armugam, Arunmozhiarasi |
collection | PubMed |
description | BACKGROUND: Phospholipase A(2 )liberates free fatty acids and lysophospholipids upon hydrolysis of phospholipids and these products are often associated with detrimental effects such as inflammation and cerebral ischemia. The neuroprotective effect of neutral phospholipase from snake venom has been investigated. RESULTS: A neutral anticoagulant secretory phospholipase A(2 )(nPLA) from the venom of Naja sputatrix (Malayan spitting cobra) has been found to reduce infarct volume in rats subjected to focal transient cerebral ischemia and to alleviate the neuronal damage in organotypic hippocampal slices subjected to oxygen-glucose deprivation (OGD). Real-time PCR based gene expression analysis showed that anti-apoptotic and pro-survival genes have been up-regulated in both in vivo and in vitro models. Staurosporine or OGD mediated apoptotic cell death in astrocytoma cells has also been found to be reduced by nPLA with a corresponding reduction in caspase 3 activity. CONCLUSION: We have found that a secretory phospholipase (nPLA) purified from snake venom could reduce infarct volume in rodent stroke model. nPLA, has also been found to reduce neuronal cell death, apoptosis and promote cell survival in vitro ischemic conditions. In all conditions, the protective effects could be seen at sub-lethal concentrations of the protein. |
format | Text |
id | pubmed-2758888 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-27588882009-10-08 A secretory phospholipase A(2)-mediated neuroprotection and anti-apoptosis Armugam, Arunmozhiarasi Cher, Charmian DN Lim, KaiYing Koh, Dawn CI Howells, David W Jeyaseelan, Kandiah BMC Neurosci Research Article BACKGROUND: Phospholipase A(2 )liberates free fatty acids and lysophospholipids upon hydrolysis of phospholipids and these products are often associated with detrimental effects such as inflammation and cerebral ischemia. The neuroprotective effect of neutral phospholipase from snake venom has been investigated. RESULTS: A neutral anticoagulant secretory phospholipase A(2 )(nPLA) from the venom of Naja sputatrix (Malayan spitting cobra) has been found to reduce infarct volume in rats subjected to focal transient cerebral ischemia and to alleviate the neuronal damage in organotypic hippocampal slices subjected to oxygen-glucose deprivation (OGD). Real-time PCR based gene expression analysis showed that anti-apoptotic and pro-survival genes have been up-regulated in both in vivo and in vitro models. Staurosporine or OGD mediated apoptotic cell death in astrocytoma cells has also been found to be reduced by nPLA with a corresponding reduction in caspase 3 activity. CONCLUSION: We have found that a secretory phospholipase (nPLA) purified from snake venom could reduce infarct volume in rodent stroke model. nPLA, has also been found to reduce neuronal cell death, apoptosis and promote cell survival in vitro ischemic conditions. In all conditions, the protective effects could be seen at sub-lethal concentrations of the protein. BioMed Central 2009-09-23 /pmc/articles/PMC2758888/ /pubmed/19775433 http://dx.doi.org/10.1186/1471-2202-10-120 Text en Copyright © 2009 Armugam et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Armugam, Arunmozhiarasi Cher, Charmian DN Lim, KaiYing Koh, Dawn CI Howells, David W Jeyaseelan, Kandiah A secretory phospholipase A(2)-mediated neuroprotection and anti-apoptosis |
title | A secretory phospholipase A(2)-mediated neuroprotection and anti-apoptosis |
title_full | A secretory phospholipase A(2)-mediated neuroprotection and anti-apoptosis |
title_fullStr | A secretory phospholipase A(2)-mediated neuroprotection and anti-apoptosis |
title_full_unstemmed | A secretory phospholipase A(2)-mediated neuroprotection and anti-apoptosis |
title_short | A secretory phospholipase A(2)-mediated neuroprotection and anti-apoptosis |
title_sort | secretory phospholipase a(2)-mediated neuroprotection and anti-apoptosis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2758888/ https://www.ncbi.nlm.nih.gov/pubmed/19775433 http://dx.doi.org/10.1186/1471-2202-10-120 |
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