A secretory phospholipase A2-mediated neuroprotection and anti-apoptosis

被引:21
作者
Armugam, Arunmozhiarasi [1 ]
Cher, Charmian D. N. [1 ]
Lim, KaiYing [1 ]
Koh, Dawn C. I. [1 ]
Howells, David W. [2 ]
Jeyaseelan, Kandiah [1 ]
机构
[1] Natl Univ Singapore, Dept Biochem, Yong Loo Lin Sch Med, Singapore 117597, Singapore
[2] Natl Stroke Res Inst, Heidelberg, Vic 3084, Australia
来源
BMC NEUROSCIENCE | 2009年 / 10卷
关键词
FOCAL CEREBRAL-ISCHEMIA; NAJA-SPUTATRIX VENOM; MICROARRAY DATA; PLASMINOGEN-ACTIVATOR; MOLECULAR-MECHANISMS; NEURITE OUTGROWTH; OXIDATIVE STRESS; CELL INJURY; IN-VITRO; A(2);
D O I
10.1186/1471-2202-10-120
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
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.
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页数:13
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