PRESYNAPTIC MECHANISMS OF SOME NEURONAL PLASTICITIES
一些神经元可塑性的突触前机制
基本信息
- 批准号:2266961
- 负责人:
- 金额:$ 14.36万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:1992
- 资助国家:美国
- 起止时间:1992-12-01 至 1998-11-30
- 项目状态:已结题
- 来源:
- 关键词:action potentials alternatives to animals in research biophysics calcium channel blockers calcium flux crayfish electrical conductance electrophysiology evoked potentials long term potentiation magnetic recording system neural facilitation neural plasticity neuropharmacology neurotransmitter transport phosphorylation potassium potassium channel sodium voltage /patch clamp
项目摘要
Our long-term objective is to define electrophysiological and biophysical
mechanisms which are responsible for the presynaptic plasticities of
facilitation, augmentation, post-tetanic potentiation and long-term
potentiation. All of these homosynaptic plasticides will be examined
using the crayfish opener excitor neuron whose nerve terminals can be
doubly penetrated a fraction of a space constant away from transmitter
release sites whose evoked and spontaneous release can be recorded from
large, identified postsynaptic muscle cells. Using this preparation, we
propose to examine whether increases in calcium currents, decreases in
several potassium conductances, and/or increases in internal calcium or
sodium concentrations contribute to any or all of these homosynaptic
plasticides. Electrophysiological and biophysical paradigms have been
carefully designed to measure each of these ionic properties.
Given the conservative evolution of many other cellular/molecular
mechanisms (including axonal conduction and synaptic transmission),
cellular/molecular mechanisms of these synaptic plasticities found at
crayfish opener excitor synapses will almost certainly be found at
mammalian synapses (including humans). Such knowledge is important
because the synaptic plasticities of facilitation, augmentation, and
post-tetanic potentiation are probably responsible for such behavioral
phenomena as arousal and sensitization, whereas long-term potentiation
may be the neuronal basis for learning and memory.
我们的长期目标是定义电生理和生物物理
项目成果
期刊论文数量(1)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Presynaptic calcium-activated potassium channels and calcium channels at a crayfish neuromuscular junction.
突触前钙激活钾通道和小龙虾神经肌肉接头处的钙通道。
- DOI:10.1152/jn.1995.73.1.178
- 发表时间:1995
- 期刊:
- 影响因子:0
- 作者:Blundon,JA;Wright,SN;Brodwick,MS;Bittner,GD
- 通讯作者:Bittner,GD
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GEORGE Davis BITTNER其他文献
GEORGE Davis BITTNER的其他文献
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{{ truncateString('GEORGE Davis BITTNER', 18)}}的其他基金
Translating Novel Peripheral Nerve Allograft Technologies Toward Clinical Use
将新型周围神经同种异体移植技术转化为临床应用
- 批准号:
10660790 - 财政年份:2023
- 资助金额:
$ 14.36万 - 项目类别:
A novel bioengineered technique to rapidly and permanently repair cut PNS nerves
一种新颖的生物工程技术,可快速永久修复切断的三七总神经系统神经
- 批准号:
9103652 - 财政年份:2015
- 资助金额:
$ 14.36万 - 项目类别:
A novel bioengineered technique to rapidly and permanently repair cut PNS nerves
一种新颖的生物工程技术,可快速永久修复切断的三七总神经系统神经
- 批准号:
8877247 - 财政年份:2012
- 资助金额:
$ 14.36万 - 项目类别:
A novel bioengineered technique to rapidly and permanently repair cut PNS nerves
一种新颖的生物工程技术,可快速永久修复切断的三七总神经系统神经
- 批准号:
8419268 - 财政年份:2012
- 资助金额:
$ 14.36万 - 项目类别:
A novel bioengineered technique to rapidly and permanently repair cut PNS nerves
一种新颖的生物工程技术,可快速永久修复切断的三七总神经系统神经
- 批准号:
8687758 - 财政年份:2012
- 资助金额:
$ 14.36万 - 项目类别:
A novel bioengineered technique to rapidly and permanently repair cut PNS nerves
一种新颖的生物工程技术,可快速永久修复切断的三七总神经系统神经
- 批准号:
8545916 - 财政年份:2012
- 资助金额:
$ 14.36万 - 项目类别:
ENHANCED REGENERATION OF NERVE AXONS BY BIOPOLYMERS
生物聚合物增强神经轴突再生
- 批准号:
2204027 - 财政年份:1994
- 资助金额:
$ 14.36万 - 项目类别:
ENHANCED REGENERATION OF NERVE AXONS BY BIOPOLYMERS
生物聚合物增强神经轴突再生
- 批准号:
2204026 - 财政年份:1994
- 资助金额:
$ 14.36万 - 项目类别:
PRESYNAPTIC MECHANISMS OF SOME NEURONAL PLASTICITIES
一些神经元可塑性的突触前机制
- 批准号:
2266960 - 财政年份:1992
- 资助金额:
$ 14.36万 - 项目类别:
PRESYNAPTIC MECHANISMS OF SOME NEURONAL PLASTICITIES
一些神经元可塑性的突触前机制
- 批准号:
3415014 - 财政年份:1992
- 资助金额:
$ 14.36万 - 项目类别:














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