ROLE OF ENTOPEDUNCULAR NUCLEUS IN KINDLED SEIZURES
内脚核在点燃癫痫发作中的作用
基本信息
- 批准号:3084051
- 负责人:
- 金额:$ 7.68万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:1987
- 资助国家:美国
- 起止时间:1987-07-01 至 1992-06-30
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
Kindling is an animal model of epilepsy that can provide
information about the neural network and potentially the
molecular basis underlying seizures. Abundant evidence suggests
that the substantia nigra (SN) promotes seizure propagation in
kindling and other models of seizures. Because the SN and the
entopeduncular nucleus (EPN), the rodent equivalent of the
primate internal pallidum, are the two output relay nuclei of the
basal ganglia, the EPN may also play a role in seizure
propagation. Preliminary evidence supports this hypothesis in the
pilocarpine model of seizures.
This project will test the hypothesis that the EPN regulates
seizure propagation, and will compare the postulated role of the
EPN with that of the SN. Several lines of experimental evidence
will be used. Microinjection of a GABA agonist into the EPN will
be used to inhibit its outflow and thereby examine its effect on
electroshock and kindled seizures in rats. Microinjection of an
excitatory amino acid, NMDA, into the EPN will be used to
enhance EPN outflow, and to examine the effect on the threshold
and duration of kindled seizures. Simultaneous extracellular
single-unit recording in the EPN and one of its monosynaptic
targets, the lateral habenular nucleus, will verify that intra-EPN
microinjection of these compounds produces the inhibition and
excitation presumed. The effect of the EPN on the development
of kindling will be tested by lesioning the structure before
kindling is established. Finally, the monosynaptic targets of the
EPN will be selectively lesioned to discover which is (are)
necessary for the role of the EPN in seizure regulation.
Results of these studies will add to the known role of the SN in
seizure regulation. Once the full neural network(s) underlying
seizure expression is (are) known, better pharmacologic or
surgical manipulation of human seizures may be possible.
点燃是一种癫痫动物模型,可以提供
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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DAVID A HOSFORD其他文献
DAVID A HOSFORD的其他文献
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{{ truncateString('DAVID A HOSFORD', 18)}}的其他基金
GABA B MECHANISMS OF ABSENCE SEIZURES IN LETHARGIC MICE
GABA B 昏睡小鼠失神发作的机制
- 批准号:
2379674 - 财政年份:1993
- 资助金额:
$ 7.68万 - 项目类别:
GABA B MECHANISMS OF ABSENCE SEIZURES IN LETHARGIC MICE
GABA B 昏睡小鼠失神发作的机制
- 批准号:
2268943 - 财政年份:1993
- 资助金额:
$ 7.68万 - 项目类别:
GABA B MECHANISMS OF ABSENCE SEIZURES IN LETHARGIC MICE
GABA B 昏睡小鼠失神发作的机制
- 批准号:
2669014 - 财政年份:1993
- 资助金额:
$ 7.68万 - 项目类别:
ROLE OF ENTOPEDUNCULAR NUCLEUS IN KINDLED SEIZURES
内脚核在点燃癫痫发作中的作用
- 批准号:
3084047 - 财政年份:1987
- 资助金额:
$ 7.68万 - 项目类别:
ROLE OF ENTOPEDUNCULAR NUCLEUS IN KINDLED SEIZURES
内脚核在点燃癫痫发作中的作用
- 批准号:
3084048 - 财政年份:1987
- 资助金额:
$ 7.68万 - 项目类别:
ROLE OF ENTOPEDUNCULAR NUCLEUS IN KINDLED SEIZURES
内脚核在点燃癫痫发作中的作用
- 批准号:
3084050 - 财政年份:1987
- 资助金额:
$ 7.68万 - 项目类别:
ROLE OF ENTOPEDUNCULAR NUCLEUS IN KINDLED SEIZURES
内脚核在点燃癫痫发作中的作用
- 批准号:
3084049 - 财政年份:1987
- 资助金额:
$ 7.68万 - 项目类别:
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