Neuroprotective role of OGR1 in brain ischemia
Neuroprotective role of OGR1 in brain ischemia
批准号:
10505248
负责人:
Xiangming Zha
金额:
$39.51万
依托单位国家:
美国
项目类别:
财政年份:
2021
资助国家:
美国
项目状态:
已结题
起止时间:
2021-10-07 至 2024-06-30
关键词:
ASIC channelAcidosisAcidsAlteplaseAttenuatedBrainBrain InjuriesBrain IschemiaBrain regionCalciumCationsCell Culture TechniquesCellsComplexCorpus striatum structureCoupledCyclic AMPCytoplasmic GranulesDataDiglyceridesDiseaseEquilibriumFDA approvedFamilyG-Protein-Coupled ReceptorsGPR4 geneGPR68 geneHippocampus (Brain)ImageIn VitroInfarctionInjuryIon ChannelIschemiaKnowledgeLeadMediatingMediator of activation proteinMetabolismMethodsMiddle Cerebral Artery OcclusionMitochondriaModelingMolecularMolecular TargetMultiple SclerosisMusN-Methyl-D-Aspartate ReceptorsNeuronal InjuryNeuronsPathway interactionsPatientsPharmaceutical PreparationsPharmacologyPrevalenceProcessPropertyProtein Kinase CProtonsReagentRegulationRodent ModelRoleSeriesSignal TransductionSliceSpinal GangliaStrokeStudy modelsSystemTestingTherapeutic InterventionTraumatic Brain Injurybasedesigndisabilityexcitotoxicityexperimental studyextracellularhippocampal pyramidal neuronmitochondrial permeability transition poremortalityneuroprotectionnew therapeutic targetnovelnovel therapeutic interventionoverexpressionpostsynapticprotective effectreceptorrelating to nervous systemsensorstroke outcomestroke therapy
中文摘要
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英文摘要
PROJECT ABSTRACT
Brain acidification occurs in excitotoxicity, following disrupted metabolism, and in multiple diseases including
ischemia, multiple sclerosis, and traumatic brain injury. Given the prevalence of acidosis in disease,
determining molecular mechanisms underlying acid signaling will have broad translational value. It has been
known for decades that acidosis is one key contributing factor to neuronal injury. Paradoxically, a relatively
mild acidosis can be protective. In recent years, a lot of progress has been made on understanding how
acidosis leads to neuronal injury. This is largely due to the discovery of acid-sensing ion channels (ASICs),
which are a family of proton gated cation channels. A series of data, including ours, show that ASICs are the
major postsynaptic proton receptor in brain neurons, and one key mediator of acidosis-induced neuronal injury.
These data on ASICs have greatly advanced our knowledge of acid signaling. However, ASICs do not appear
to explain the protective effect of acidosis. In our preliminary studies, we found that ovarian cancer G protein
coupled receptor 1 (OGR1), a proton-sensitive G protein coupled receptor (GPCR), is widely expressed in the
brain. In addition, OGR1 mediates acid-induced signaling in hippocampal slices. Our data further suggest that
OGR1 mediates a protective pathway in acidotic and ischemic conditions. Here, we will use middle cerebral
artery occlusion, a widely used rodent model for studying ischemia-induced brain injury, and determine
whether OGR1 activation leads to neuroprotection following ischemia. To better understand the mechanism,
we will use in vitro cell culture and slice models to determine downstream signaling that mediates the effect of
OGR1. Results obtained from the proposed study will uncover novel protective mechanisms mediating
extracellular acid signaling, and provide potential molecular targets for the design of novel therapeutic
approaches to alleviate ischemia-induced brain injury.
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DOI:
10.1096/fj.202002511r
发表时间:
2021-04
期刊:
FASEB journal : official publication of the Federation of American Societies for Experimental Biology
影响因子:
--
作者:
[Zhou G, Wang T, Zha XM]
通讯作者:
Zha XM
DOI:
--
发表时间:
2017-11
期刊:
International journal of physiology, pathophysiology and pharmacology
影响因子:
--
作者:
[Yu-Qing Jiang;Xiang-ming Zha]
通讯作者:
Yu-Qing Jiang;Xiang-ming Zha
DOI:
10.1177/0271678x221089074
发表时间:
2022-08
期刊:
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM
影响因子:
6.3
作者:
[Zha, Xiang-ming, Xiong, Zhi-Gang, Simon, Roger P.]
通讯作者:
Simon, Roger P.
DOI:
10.3389/fnins.2021.692217
发表时间:
2021
期刊:
Frontiers in neuroscience
影响因子:
4.3
作者:
[Zhou G, Zha XM]
通讯作者:
Zha XM
DOI:
10.3390/biom10091264
发表时间:
2020-09-02
期刊:
Biomolecules
影响因子:
5.5
作者:
[Jiang Q, Peterson AM, Chu Y, Yao X, Zha XM, Chu XP]
通讯作者:
Chu XP
共 6 条
Mechanistic inquiry of GPR68-mediated neuroprotection against post-stroke deficits and VCID
-
批准号:10807584
-
项目类别:
-
资助金额:$62.71万
-
财政年份:2023
-
负责人:Xiangming Zha
-
依托单位:
GPR4 in blood brain barrier dysfunction in brain ischemia
-
批准号:10711110
-
项目类别:
-
资助金额:$39.13万
-
财政年份:2022
-
负责人:Xiangming Zha
-
依托单位:
GPR4 in blood brain barrier dysfunction in brain ischemia
-
批准号:10522141
-
项目类别:
-
资助金额:$38.73万
-
财政年份:2022
-
负责人:Xiangming Zha
-
依托单位:
GPR4 in blood brain barrier dysfunction in brain ischemia
-
批准号:10652655
-
项目类别:
-
资助金额:$38.72万
-
财政年份:2022
-
负责人:Xiangming Zha
-
依托单位:
Neuroprotective role of OGR1 in brain ischemia
-
批准号:9470605
-
项目类别:
-
资助金额:$37.46万
-
财政年份:2017
-
负责人:Xiangming Zha
-
依托单位:
国内基金
海外基金
肿瘤微环境因子Lactic acidosis在肿瘤细胞耐受葡萄糖剥夺中的作用机制研究
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批准号:81301707
-
项目类别:青年科学基金项目
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资助金额:23.0万元
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批准年份:2013
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负责人:吴昊
-
依托单位: