The Physiology of Extra Synaptic NMDA Receptors
The Physiology of Extra Synaptic NMDA Receptors
批准号:
7047251
负责人:
DIANA Leslie PETTIT
金额:
$18.67万
依托单位国家:
美国
项目类别:
财政年份:
2006
资助国家:
美国
项目状态:
已结题
起止时间:
2006-06-07 至 2008-05-31
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): N-methyl-D-aspartate receptor (NMDAR) activation can result in both long and short-term plasticity, promote cell survival, initiate cell death, and is also critical for normal synaptogenesis during development. A number of studies suggest that the consequences of NMDAR activation can vary widely depending on receptor localization, temporal characteristics, and size of the signal (Bito et al., 1996; Fields et al., 1997; Hardingham et al., 1999; Chawla and Bading, 2001; Hardingham et al., 2001a, b). The focus of this study is the physiological role of extrasynaptic vs. synaptic NMDARs. Cultured neuron studies have suggested that NMDARs can exist as synaptic NR1/NR2A heteromers and extrasynaptic NR1/NR2B heteromers. These two receptor types may be coupled to very different cellular processes, with calcium entry through extrasynaptic NMDARs activating cell death mechanisms and LTD rather than LTP (Lu et al., 2001; Hardingham et al., 2002). Although these experiments have provided valuable clues about possible spatial and functional segregation of extrasynaptic NMDARs in neurons, the existence and physiological relevance of these receptors in intact tissue remains unclear. Our preliminary results, which are significantly different from culture measurements, suggest that approximately 40% of the NMDAR population is extrasynaptic in acute hippocampal slice dendrites. This indicates that there is a large pool of extrasynaptic receptors available for activation during periods of high presynaptic activity. Our underlying hypothesis is that extrasynaptic NMDARs participate in neuronal interactions under pathological and physiologically relevant conditions. This hypothesis will be tested by determining the size of the extrasynaptic NMDAR pool, subunit composition, and developmental expression in acute hippocampal brain slices. We will determine the conditions under which extrasynaptic receptors can participate in transmission and their role in the expression of long-term potentiation or depression.
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会议论文
Inhibitory Microcircuits in the Piriform Cortex
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批准号:8112514
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项目类别:
-
资助金额:$24.1万
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财政年份:2010
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负责人:DIANA Leslie PETTIT
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依托单位:
Inhibitory Microcircuits in the Piriform Cortex
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批准号:7991093
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项目类别:
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资助金额:$20.75万
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财政年份:2010
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负责人:DIANA Leslie PETTIT
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依托单位:
The Physiology of Extra Synaptic NMDA Receptors
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批准号:7244067
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项目类别:
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资助金额:$21.76万
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财政年份:2006
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负责人:DIANA Leslie PETTIT
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依托单位:
Kainate Receptors in Synaptic Transmission
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批准号:6925015
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项目类别:
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资助金额:$33.69万
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财政年份:2005
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负责人:DIANA Leslie PETTIT
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依托单位:
Kainate Receptors in Synaptic Transmission
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批准号:7406671
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项目类别:
-
资助金额:$32.76万
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财政年份:2005
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负责人:DIANA Leslie PETTIT
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依托单位:
Kainate Receptors in Synaptic Transmission
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批准号:7017687
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项目类别:
-
资助金额:$33.69万
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财政年份:2005
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负责人:DIANA Leslie PETTIT
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依托单位:
Kainate Receptors in Synaptic Transmission
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批准号:7217913
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项目类别:
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资助金额:$32.76万
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财政年份:2005
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负责人:DIANA Leslie PETTIT
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依托单位:
MICROMAPPING OF LEAD INDUCED CHANGES TO NMDA RECEPTORS
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批准号:6658035
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项目类别:
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资助金额:$10.74万
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财政年份:2001
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负责人:DIANA Leslie PETTIT
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依托单位:
MICROMAPPING OF LEAD INDUCED CHANGES TO NMDA RECEPTORS
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批准号:6132592
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项目类别:
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资助金额:$10.18万
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财政年份:2001
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负责人:DIANA Leslie PETTIT
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依托单位:
MICROMAPPING OF LEAD INDUCED CHANGES TO NMDA RECEPTORS
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批准号:6524699
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项目类别:
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资助金额:$10.66万
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财政年份:2001
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负责人:DIANA Leslie PETTIT
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依托单位:
MODIFICATION OF SELECTED SYNAPTIC TARGETS IN LTP
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批准号:2241316
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项目类别:
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资助金额:$1.18万
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财政年份:1993
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负责人:DIANA Leslie PETTIT
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依托单位:
MODIFICATION OF SELECTED SYNAPTIC TARGETS IN LTP
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批准号:2241317
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项目类别:
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资助金额:$1.0万
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财政年份:1993
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负责人:DIANA Leslie PETTIT
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依托单位:
海外基金