CHRONIC POST ISCHEMIC BRAIN ALKALOSIS
CHRONIC POST ISCHEMIC BRAIN ALKALOSIS
批准号:
2267630
负责人:
MICHAEL CHOPP
金额:
$20.28万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
1991
资助国家:
美国
项目状态:
已结题
起止时间:
1991-05-01 至 1995-04-30
中文摘要
点击翻译按钮获取中文摘要
英文摘要
DESCRIPTION (Adapted from the applicant's abstract): The specific aim of
this study is to clarify the relationship between post ischemic brain
tissue alkalosis and ischemic neuronal damage, and ultimately to
demonstrate that brain alkalosis, as measured by NMR, is a useful marker of
neuronal injury. The following Specific Aims are in accord with this goal:
1) To measure brain pH, using in vivo 31P phosphorous NMR spectroscopy
serially for one week following the induction of ischemia, and to also
measure neuronal damage in the same tissue. These measurements will be
performed as a function of the duration of transient forebrain ischemia, as
well as for a "protective" hypothermic intervention in the rat. The
hypothesis being tested is that the extent of neuronal cell damage is
directly correlated with the magnitude, onset time and duration of
alkalosis detected from the same tissue. The basis for this correlation is
that the temporal profile of alkalosis reflects cellular inflammatory
processes, associated with neuronal damage. 2) To measure, at particular
time points after ischemia, inflammatory cellular response and glial
proliferation, neuronal damage and brain tissue pH, as a function of the
duration of transient forebrain ischemia and for a hypothermic
intervention. The hypothesis being tested is that inflammatory cellular
response and glial proliferation is directly correlated to neuronal damage;
hence brain tissue alkalosis is directly correlated to neuronal damage. 3)
To measure, in conjunction with the above studies, cerebral blood flow and
relative concentrations of brain high energy phosphates and lactates.
These measurements will address the relationship between brain tissue
alkalosis, and CBF and metabolic changes in the tissue.
It is proposed that post ischemic brain pH changes will be closely coupled
to ultimate tissue viability, and that the studies will therefore highlight
the potential diagnostic significance of chronic pH measurements in stroke
patients.
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Post-ischemic brain tissue alkalosis suppressed by U74006F.
U74006F 抑制缺血后脑组织碱中毒。
DOI:
10.1016/0022-510x(93)90045-z
发表时间:
1993
期刊:
Journal of the neurological sciences
影响因子:
4.4
作者:
[VandeLinde,AM, Chopp,M, Lee,SA, Schultz,LR, Welch,KM]
通讯作者:
Welch,KM
Delayed intravenous administration of basic fibroblast growth factor (bFGF) reduces infarct volume in a model of focal cerebral ischemia/reperfusion in the rat.
延迟静脉注射碱性成纤维细胞生长因子(bFGF)可减少大鼠局灶性脑缺血/再灌注模型中的梗塞体积。
DOI:
--
发表时间:
1996
期刊:
Journal of the neurological sciences.
影响因子:
--
作者:
[Jiang,N, Finklestein,SP, Do,T, Caday,CG, Charette,M, Chopp,M]
通讯作者:
Chopp,M
Effects of moderate hyperglycemia on the temporal profile of brain tissue intracellular pH and [Mg2+] after global cerebral ischemia in rats.
中度高血糖对大鼠全脑缺血后脑组织细胞内 pH 和 [Mg2] 时间分布的影响。
DOI:
10.1016/0022-510x(94)00254-l
发表时间:
1995
期刊:
Journal of the neurological sciences
影响因子:
4.4
作者:
[Hurd,K, Chopp,M, VandeLinde,AM, Li,Y, Spencer,T]
通讯作者:
Spencer,T
Transforming growth factor beta-1 (TGF-beta 1) potentiates IL1 alpha-induced IL6 mRNA and cytokine protein production in a human astrocytoma cell line.
转化生长因子 beta-1 (TGF-beta 1) 可增强人星形细胞瘤细胞系中 IL1 α 诱导的 IL6 mRNA 和细胞因子蛋白的产生。
DOI:
--
发表时间:
1993
期刊:
Oncology research
影响因子:
3.1
作者:
[Gautam,SC, Noth,CJ, Niewenhuis,LM, Janakiraman,N, Kim,JS, Chopp,M]
通讯作者:
Chopp,M
Vasculotide promotes cognitive improvement in rats with vascular dementia
-
批准号:10605198
-
项目类别:
-
资助金额:$37.63万
-
财政年份:2019
-
负责人:MICHAEL CHOPP
-
依托单位:
Diabetic stroke cardiac dysfunction; treatment with CD133+Exosomes
-
批准号:10242634
-
项目类别:
-
资助金额:$46.16万
-
财政年份:2018
-
负责人:MICHAEL CHOPP
-
依托单位:
miR-17-92 exosome treatment of stroke
-
批准号:8996733
-
项目类别:
-
资助金额:$32.48万
-
财政年份:2015
-
负责人:MICHAEL CHOPP
-
依托单位:
miR-17-92 exosome treatment of stroke
-
批准号:8886032
-
项目类别:
-
资助金额:$32.48万
-
财政年份:2015
-
负责人:MICHAEL CHOPP
-
依托单位:
MSCs Induce Brain Plasticity via tPA
-
批准号:8104726
-
项目类别:
-
资助金额:$30.03万
-
财政年份:2011
-
负责人:MICHAEL CHOPP
-
依托单位:
MSCs Induce Brain Plasticity via tPA
-
批准号:8450131
-
项目类别:
-
资助金额:$28.38万
-
财政年份:2011
-
负责人:MICHAEL CHOPP
-
依托单位:
MSCs Induce Brain Plasticity via tPA
-
批准号:8248705
-
项目类别:
-
资助金额:$30.03万
-
财政年份:2011
-
负责人:MICHAEL CHOPP
-
依托单位:
MSCs Induce Brain Plasticity via tPA
-
批准号:8657975
-
项目类别:
-
资助金额:$30.03万
-
财政年份:2011
-
负责人:MICHAEL CHOPP
-
依托单位:
Administration
-
批准号:7252236
-
项目类别:
-
资助金额:$5.88万
-
财政年份:2007
-
负责人:MICHAEL CHOPP
-
依托单位:
Treatment of Neural Injury with MSCs
-
批准号:7073312
-
项目类别:
-
资助金额:$121.62万
-
财政年份:2003
-
负责人:MICHAEL CHOPP
-
依托单位:
Core--Biostatistical
-
批准号:6785784
-
项目类别:
-
资助金额:$23.9万
-
财政年份:2003
-
负责人:MICHAEL CHOPP
-
依托单位:
Treatment of Neural Injury with MSCs
-
批准号:6899835
-
项目类别:
-
资助金额:$120.16万
-
财政年份:2003
-
负责人:MICHAEL CHOPP
-
依托单位:
Treatment of Neural Injury with MSCs
-
批准号:7263882
-
项目类别:
-
资助金额:$120.88万
-
财政年份:2003
-
负责人:MICHAEL CHOPP
-
依托单位:
Treatment of Neural Injury with MSCs
-
批准号:6616466
-
项目类别:
-
资助金额:$119.48万
-
财政年份:2003
-
负责人:MICHAEL CHOPP
-
依托单位:
Treatment of Neural Injury with MSCs
-
批准号:6771121
-
项目类别:
-
资助金额:$118.46万
-
财政年份:2003
-
负责人:MICHAEL CHOPP
-
依托单位:
Treatment of Neural Injury with MSCs
-
批准号:7167544
-
项目类别:
-
资助金额:$7.25万
-
财政年份:2003
-
负责人:MICHAEL CHOPP
-
依托单位:
LIPOSOME AND BSO ENHANCEMENT OF PHOTODYNAMIC THERAPY
-
批准号:6563817
-
项目类别:
-
资助金额:$22.84万
-
财政年份:2002
-
负责人:MICHAEL CHOPP
-
依托单位:
ANTIPLATELET AGGREGATION THERAPY FOR EMBOLIC STROKE
-
批准号:6660978
-
项目类别:
-
资助金额:$17.32万
-
财政年份:2002
-
负责人:MICHAEL CHOPP
-
依托单位:
CORE--BIOSTATISTICS
-
批准号:6660979
-
项目类别:
-
资助金额:$17.32万
-
财政年份:2002
-
负责人:MICHAEL CHOPP
-
依托单位:
CORE--BIOSTATISTICS
-
批准号:6573862
-
项目类别:
-
资助金额:$17.32万
-
财政年份:2001
-
负责人:MICHAEL CHOPP
-
依托单位:
海外基金