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pubmed-article:19387543pubmed:dateCreated2009-5-18lld:pubmed
pubmed-article:19387543pubmed:abstractTextCaspase-12 has been localized to endoplasmic reticulum (ER) and showed to involve ER stress-induced apoptosis. In the present work we investigated the temporospatial alterations of caspase-12 immunoreactivity in the penumbra following cerebral ischemia/reperfusion in rabbit. Transient cerebral ischemia was produced by intraluminal occlusion of the middle cerebral artery for 2 h followed by 1 h, 6 h, 1 day, 3 days, 7 days and 14 days of reperfusion. Caspase-12 immunohistochemistry was first increased in the penumbra 1 h after reperfusion, with a peak at day 1 to day 3, and then gradually decreased to basal level at day 14. The number of TUNEL-positive cells and ultrastructural observation of brain sections in the penumbra showed a similar change at the same time points. ER mediated by caspase-12 participated in apoptosis induced by cerebral ischemia/reperfusion injury, which may provide a new area for therapeutic intervention to ameliorate outcomes following cerebral ischemia.lld:pubmed
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pubmed-article:19387543pubmed:authorpubmed-author:YingLiLlld:pubmed
pubmed-article:19387543pubmed:authorpubmed-author:LiChun-YanCYlld:pubmed
pubmed-article:19387543pubmed:authorpubmed-author:YangJi-PingJPlld:pubmed
pubmed-article:19387543pubmed:authorpubmed-author:LiuHuai-JunHJlld:pubmed
pubmed-article:19387543pubmed:authorpubmed-author:LiuRui-ChunRClld:pubmed
pubmed-article:19387543pubmed:authorpubmed-author:WangCang-HaiC...lld:pubmed
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pubmed-article:19387543pubmed:volume30lld:pubmed
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pubmed-article:19387543pubmed:pagination227-32lld:pubmed
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pubmed-article:19387543pubmed:year2009lld:pubmed
pubmed-article:19387543pubmed:articleTitleEndoplasmic reticulum in the penumbra following middle cerebral artery occlusion in the rabbit.lld:pubmed
pubmed-article:19387543pubmed:affiliationDepartment of Medical Imaging, The Second Hospital of Hebei Medical University, 215 West Heping Road, Shijiazhuang, 050000, Hebei Province, China. huaijun_hb@yahoo.com.cnlld:pubmed
pubmed-article:19387543pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:19387543pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
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