Please use this identifier to cite or link to this item:
http://hdl.handle.net/11455/38336
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Lin, C.H. | en_US |
dc.contributor.author | 葛其梅 | zh_TW |
dc.contributor.author | Lu, Y.Z. | en_US |
dc.contributor.author | Cheng, F.C. | en_US |
dc.contributor.author | Chu, L.F. | en_US |
dc.contributor.author | Hsueh, C.M. | en_US |
dc.date | 2005 | zh_TW |
dc.date.accessioned | 2014-06-06T08:00:43Z | - |
dc.date.available | 2014-06-06T08:00:43Z | - |
dc.identifier.issn | 0304-3940 | zh_TW |
dc.identifier.uri | http://hdl.handle.net/11455/38336 | - |
dc.description.abstract | An in vitro ischemia model was used to determine the molecular mechanisms responsible for the ischemia-induced neuronal cell death. Additionally, the neuronal protective mechanisms of anti-apoptotic drugs against ischemia were also evaluated. In this study, the primary neuronal cultures were incubated in an anoxic chamber with 95% of N-2 and 5% of CO2 for various times. The death rate, degree of the apoptotic damage, reduction of mitochondrial membrane potential, translocation of Bax, release of cytochrome C and activation of caspase-9 and -3 were determined at each time point. Results showed that a Bax-regulated mitochondria- mediated apoptosis is responsible for the in vitro ischemia-induced neuronal death. Reduction in mitochondrial membrane potential plays no role in triggering this apoptosis. Furthermore, the anti-apoptotic drugs: furosemide (a Bax blocker) and ZVAD-fmk (caspase inhibitor) but not cyclosporine A (a NIPT pore blocker), significantly protected the neurons against ischemia-induced damage. This provides an additional consideration in the future selection of new anti-ischemic drugs. (C) 2005 Elsevier Ireland Ltd. All rights reserved. | en_US |
dc.language.iso | en_US | zh_TW |
dc.relation | Neuroscience Letters | en_US |
dc.relation.ispartofseries | Neuroscience Letters, Volume 387, Issue 1, Page(s) 22-27. | en_US |
dc.relation.uri | http://dx.doi.org/10.1016/j.neulet.2005.06.070 | en_US |
dc.subject | in vitro ischemia | en_US |
dc.subject | neuronal cell death | en_US |
dc.subject | apoptosis | en_US |
dc.subject | mitochondria | en_US |
dc.subject | Bax | en_US |
dc.subject | caspases | en_US |
dc.subject | furosemide | en_US |
dc.subject | ZVAD-fmk | en_US |
dc.subject | permeability transition | en_US |
dc.subject | cytochrome-c | en_US |
dc.subject | membrane | en_US |
dc.subject | damage | en_US |
dc.subject | activation | en_US |
dc.subject | mechanisms | en_US |
dc.subject | necrosis | en_US |
dc.subject | channel | en_US |
dc.title | Bax-regulated mitochondria-mediated apoptosis is responsible for the in vitro ischemia induced neuronal cell death of Sprague Dawley rat | en_US |
dc.type | Journal Article | zh_TW |
dc.identifier.doi | 10.1016/j.neulet.2005.06.070 | zh_TW |
item.grantfulltext | none | - |
item.openairetype | Journal Article | - |
item.languageiso639-1 | en_US | - |
item.fulltext | no fulltext | - |
item.cerifentitytype | Publications | - |
item.openairecristype | http://purl.org/coar/resource_type/c_18cf | - |
Appears in Collections: | 生命科學系所 |
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