Forensic Neuropathological Studies on Presenile and Senile Dementias
| Project/Area Number |
01570334
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| Research Category |
Grant-in-Aid for General Scientific Research (C)
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| Allocation Type | Single-year Grants |
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| Research Field |
Legal medicine
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| Research Institution | Shiga University of Medical Science |
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Principal Investigator |
TATSUNO Yoshitsugu Shiga University of Medical Science, Department of Legal Medicine Professor, 医学部, 教授 (80030831)
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| Co-Investigator(Kenkyū-buntansha) |
YAMADA Mitsuko Shiga University of Medical Science, Department of Legal Medicine, Assistant, 医学部, 助手 (80145911)
YAMAMOTO Yoshio Shiga University of medical Science, Department of Legal Medicine, Assistant, 医学部, 助手 (60111902)
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| Project Period (FY) |
1989 – 1990
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| Project Status |
Completed (Fiscal Year 1990)
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| Budget Amount *help |
¥1,400,000 (Direct Cost: ¥1,400,000)
Fiscal Year 1990: ¥600,000 (Direct Cost: ¥600,000)
Fiscal Year 1989: ¥800,000 (Direct Cost: ¥800,000)
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| Keywords | Neuropatholgy / Alzheimer's disease / Glial fibrillary acidic protein (GFAP) / Senile plaque / Amyloid / Aluminium / Neurofibrillary change / 海馬 / アルツハイマ-原線維変化 / 家兎 / 剖検診断基準 |
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| Research Abstract |
Alzheimer-type dementia (ATD) was discussed not only from the aspects of forensic neuropathology by using various techniques for general stains and silver-impregnation, but also immunohistochemically by using antiserum against glial fibrillary acidic protein which is a specific marker for astrocytes.
There were marked differences in microscopic findings between the ATD group and control groups of elderly subjects whose intellectures have been maintained. The main histlogical features of ATD were presence of numerous senile plaques and neurofibrillary changes, both of which were thought to be helpful diagnosis markers.
Double stains by glial fibrillary acidic protein (GFAP) stain using avidin-biotin peroxidase complex (ABC) method and Congo red stain were performed. By the former stain, typical senile plaques, encircled by reactive astrocytes and penetrated interiorly by their processes, were demonstrated. By the latter stain, amyloid core was well detected. Another method which is partic
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ularly sensitive to amyloid, such as amyloid core or amyloid angiopathy, thioflavin S stain. Immunohistochemical stains for glial fibrillary acidic protein demonstrated an intense participation within the plaques by processes of reactive astrocytes.
Using the autopsy criteria for the diagnosis of Alzheimer's disease reported by Khachturian, senile plaques were counted on microscopic magnification x200 field. Numerous plaques satisfying thoroughly the criteria were detected. The report by Blessed et al. that there is a highly significant correlation between mean plaque counts in sections of cerebral cortex of elderly subjects and degrees of dementia is very helpful for forensic pathologists and is highly evaluated.
There has been a report on the increase of aluminium in Ammon's horns in brains of Alzheimer's disease (Crapper et al, 1973).
In the present study, aluminum phosphate was injected in the cerebellomedullar cistern, subdural space and brain substance of 17 rabbits. In 16 out of total rabbits, except one that died one-half day after injection, findings very similar to Alzheimer neurofibrillary changes were recognized, especially in hippocampus. Less
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Report
(3 results)
Research Products
(13 results)
