Prostaglandin synthesis in response to spreading depression and focal brain ischemia
前列腺素合成对扩散性抑郁症和局灶性脑缺血的反应
基本信息
- 批准号:15591559
- 负责人:
- 金额:$ 2.24万
- 依托单位:
- 依托单位国家:日本
- 项目类别:Grant-in-Aid for Scientific Research (C)
- 财政年份:2003
- 资助国家:日本
- 起止时间:2003 至 2005
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
Temporal and topographic profiles of cyclooxygenase-2 (COX-2) expression and prostaglandins as well as [^<123>I]iomazenil distribution during 24 hours of focal brain ischemia in rats were examined. We demonstrated that prostaglandin production as well as COX-2 expression in ischemic tissues depended on the degree and duration of the reduction in cerebral blood flow (Yokota C, et al.,2004). We also confirmed that [^<123>I]iomazenil should be a useful marker of neuronal viability using histopathological findings (Kaji T, et al.2004).COX-2 was reported to be induced in the infarcted human brain. Spreading depression (SD) is thought to play a role in this induction. Thus, we correlated the expression of SD-associat.ed genes with COX-2 production in brains after SD. We showed that the bilateral induction of expression of the S-100A9 gene in response to SD was associated with COX-2 activation (Yokota C. et al.2005).We hypothesized that SD, evoked after ischemic insult, might contribute to the process of reconstitution of neural networks via the activation of SD-associated genes as a result of COX-2 production in the hemisphere contralateral to the ischemia.
检查了大鼠局灶性脑缺血24小时期间环氧合酶-2(考克斯-2)表达和前列腺素以及[^<123>I]碘马唑分布的时间和地形图。我们证明了缺血组织中前列腺素的产生以及考克斯-2的表达取决于脑血流减少的程度和持续时间(Yokota C,et al.,2004年)。我们还<123>使用组织病理学发现证实[13 I]iomazenil应该是神经元活力的有用标志物(Kaji T,et al.2004)。据报道,考克斯-2在梗塞人脑中被诱导。扩散性抑制(SD)被认为在这种诱导中起作用。因此,我们将SD相关艾德基因的表达与SD后脑中考克斯-2的产生相关联。我们发现,响应SD的S-100 A9基因表达的双侧诱导与考克斯-2激活有关(Yokota C.我们假设,在缺血损伤后诱发的SD可能有助于通过SD相关基因的激活而重建神经网络的过程,所述SD相关基因的激活是缺血对侧半球中产生考克斯-2的结果。
项目成果
期刊论文数量(42)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Characterisation of [^<123>I] iomazenil distribution in a rat model ofocal cerebral ischaemia in relation to histopathological findings
大鼠局灶性脑缺血模型中[^ 123 I]碘马西尼分布的表征与组织病理学结果的关系
- DOI:
- 发表时间:2004
- 期刊:
- 影响因子:0
- 作者:Kaji T;Kuge Y;Yokota C;Tagaya M;Inoue H;Shiga T;Minematsu K;Tamaki N
- 通讯作者:Tamaki N
Kaji T., Kuge Y., Yokota C et al.: "Characterisation of [^<123>I] iomazenil distribution in a rat model of focal cerebral ischaemia in relation to histopathological findings."European Journal of Nuclear Medicine and Molecular Imaging. 31. 64-70 (2004)
Kaji T.、Kuge Y.、Yokota C等人:“与组织病理学结果相关的局灶性脑缺血大鼠模型中[^ 123 I] iomazenil分布的特征。”欧洲核医学和分子成像杂志。
- DOI:
- 发表时间:
- 期刊:
- 影响因子:0
- 作者:
- 通讯作者:
PET and Molecular Imaging -State of the art and future perspectives-
PET 和分子成像 - 最先进的技术和未来的前景 -
- DOI:
- 发表时间:2004
- 期刊:
- 影响因子:0
- 作者:藤林 康久;Kuge Y 他
- 通讯作者:Kuge Y 他
Early neurological deterioration represents recurrent attack in acute small non-lacunae storoke
早期神经功能恶化代表急性小非腔隙性脑卒中的反复发作
- DOI:
- 发表时间:2004
- 期刊:
- 影响因子:0
- 作者:Matsumoto N;Kimura K;Yokota C;Yonemura K;Wada K;Uchino M;Minematsu K
- 通讯作者:Minematsu K
Post-ischemic cyclooxygenase-2 expression is regulated by the extent of cerebral blood flow reduction in non-human primates.
非人灵长类动物缺血后 cyclooxygenase-2 的表达受到脑血流量减少程度的调节。
- DOI:
- 发表时间:2003
- 期刊:
- 影响因子:0
- 作者:Yokota C 他
- 通讯作者:Yokota C 他
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YOKOTA Chiaki其他文献
YOKOTA Chiaki的其他文献
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{{ truncateString('YOKOTA Chiaki', 18)}}的其他基金
Clinical implication of biomarker for patients with acute stroke
生物标志物对急性脑卒中患者的临床意义
- 批准号:
23592110 - 财政年份:2011
- 资助金额:
$ 2.24万 - 项目类别:
Grant-in-Aid for Scientific Research (C)
Gene expression and protein synthesis after transient focal ischemia under an enriched environment in rats
富集环境下大鼠短暂局灶性缺血后基因表达和蛋白质合成
- 批准号:
18591619 - 财政年份:2006
- 资助金额:
$ 2.24万 - 项目类别:
Grant-in-Aid for Scientific Research (C)
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