| Project/Area Number |
07671044
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| Research Category |
Grant-in-Aid for Scientific Research (C)
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| Allocation Type | Single-year Grants |
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| Section | 一般 |
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| Research Field |
Psychiatric science
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| Research Institution | Tohoku University |
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Principal Investigator |
SATO Mitumoto Tohoku University-School of Medicine-Proffessor, 医学部, 教授 (70033321)
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| Co-Investigator(Kenkyū-buntansha) |
SINDO Katuhiro Tohoku University, School of Medicine, Department of Psychiatry, Medical stuff, 医学部・付属病院, 医員
FUSE Yuji Tohoku University, School of Medicine, Department of Psychiatry, Associate Proff, 医学部・付属病院, 助教授 (90125683)
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| Project Period (FY) |
1995 – 1996
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| Project Status |
Completed (Fiscal Year 1996)
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| Budget Amount *help |
¥2,300,000 (Direct Cost: ¥2,300,000)
Fiscal Year 1996: ¥1,200,000 (Direct Cost: ¥1,200,000)
Fiscal Year 1995: ¥1,100,000 (Direct Cost: ¥1,100,000)
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| Keywords | Kindling / Mesial Temporal sclerosis / Hippocampal EEG suppression / Sprouting / cell loss / Apoptosis / てんかん動物モデル / 海馬硬化 / TUNEL法 |
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| Research Abstract |
Mesial temporal sclerosis (MTS) refers to cell loss, gliosis involving hippocampus and often, other mesial temporal structures, and recent research demonstrated synaptic reorganization (sprouting) in the hippocampus. MTS is the most common legion in temporal lobes resected for intractable seizures. There had been considerable debate over whether MTS is cause or effect of epilepsy, but it is still unclear.
Purpose of this study is to evaluate using kinding model 1. the relation between post ictal EEG suppression that may be caused by local ischemic change, and sprouting or cell loss in the hilus of hippocampus and next 2. to investigated the degenerating process of the hippocampal pyramidal neurons whether cell loss is necrosis or apoptosis by using in situ nick-end labeling of biotinylated dUTP mediated by terminal deoxytransferase (TUNEL) methods.
The results were 1. there were strong correlation between EEG suppression and cell loss, but also cell loss correlate with number of seizures and afterdischarge duration. So that we could not determine especial factor relate with cell loss, sprouting did not correlate with EEG suppression, 2. there were no TUNEL positive neuron in kindling or over-kindling hippocampus.
This result 2. may indicate the cell loss is not apoptosis and also is not necrosis. Because TUNEL method detect DNA fragments. This means there is no neuronal death in kindling brain which neglect previous data. The reason why this discrepancy occur is unknown. To solve this problem we must demonstrate clearly that necrotic cell or degenerative cell do not exist in kindling hippocampus.
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