Prostaglandin synthesis in response to spreading depression and focal brain ischemia
Prostaglandin synthesis in response to spreading depression and focal brain ischemia
批准号:
15591559
负责人:
YOKOTA Chiaki
金额:
$2.24万
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
项目状态:
已结题
起止时间:
2003 至 2005
中文摘要
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英文摘要
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.
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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:
European Journal of Nuclear Medicine and Molecular Imaging 31
影响因子:
--
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:
--
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:
--
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:
Journal of the Neurological Sciences 217
影响因子:
--
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:
Neurosci Lett. 341(1)
影响因子:
--
作者:
[Yokota C 他]
通讯作者:
Yokota C 他
共 19 条
Clinical implication of biomarker for patients with acute stroke
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批准号:23592110
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项目类别:Grant-in-Aid for Scientific Research (C)
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资助金额:$3.24万
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财政年份:2011
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负责人:YOKOTA Chiaki
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依托单位:
Gene expression and protein synthesis after transient focal ischemia under an enriched environment in rats
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批准号:18591619
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项目类别:Grant-in-Aid for Scientific Research (C)
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资助金额:$2.62万
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财政年份:2006
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负责人:YOKOTA Chiaki
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依托单位:
海外基金