Immunohistochemical studies on early changes of components of the nervous system after head injury and application to forensic diagnosis
颅脑损伤后神经系统组成早期变化的免疫组织化学研究及其在法医学诊断中的应用
基本信息
- 批准号:10670395
- 负责人:
- 金额:$ 1.66万
- 依托单位:
- 依托单位国家:日本
- 项目类别:Grant-in-Aid for Scientific Research (C)
- 财政年份:1998
- 资助国家:日本
- 起止时间:1998 至 1999
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
1. Immunohistochemical studies on axonal injury after head trauma: Further studies were performed to determine whether immunostaining for neuron-specific enolase (NSE) can detect early post-traumatic axonal changes. NSE as well as amyloid precursor protein (APP) could label so-called axonal bulbs and swollen axons in cases with only 1.5 hours' survival after head trauma, so that NSE should be one of useful markers for detection of early axonal changes.2. Changes of astrocytes after brain injury: Antibodies against glial fibrillary acidic protein (GFAP), S100 protein, vimentin, laminin and glutamine synthetase (GS) were used. Immunostaining for GFAP and S100 labelled both reactive astrocytes in cases of head injury with more than 7 days' survival and swollen astrocytes in cases with 9 hours' to 7 days' survival. Further, in cases with less than 1.5 hours' survival, clasmatodendrosis and pyknosis of the nucleus were detected by GFAP and S100 staining. Immunostaining for vimentin, laminin and GS also labelled these astrocytes, suggesting that immunostaining for astrocytes should be useful for evaluating early brain damage after head injury.3. Changes of oligodendrocytes after brain injury: Immnostaining for CNPase label oligodendrocytes of head trauma, though did not label cells of control brain. Therefore it is suggested that CNPase staining is very useful for detection of early oligodendrocytic changes after head injury.4. Changes of microglia after brain injury: Lectin staining for Ricinus Communis agglutinin-1 (RCA1) labelled so-called foamy cells in cases of head injury with more than 2 weeks' survival and hypertrophic microglia in cases with more than 9 hours' survival, so that lectin staining for RCA1 may be useful for estimating the duration of posttraumatic survival.
1.头部创伤后轴突损伤的免疫组织化学研究:进行进一步研究以确定神经元特异性烯醇化酶(NSE)的免疫染色是否可以检测早期创伤后轴突变化。结论:1. NSE和淀粉样前体蛋白(APP)均可在脑外伤后存活仅1.5小时的病例中标记出所谓的轴突球和肿胀的轴突,因此NSE可作为检测早期轴突改变的有用标志物之一.脑损伤后星形胶质细胞的变化:采用胶质细胞酸性蛋白(GFAP)、S 100蛋白、波形蛋白、层粘连蛋白和谷氨酰胺合成酶(GS)抗体。GFAP和S100的免疫染色既标记了存活超过7天的脑损伤病例中的反应性星形胶质细胞,也标记了存活9小时至7天的病例中的肿胀星形胶质细胞。在存活时间小于1.5小时的病例中,GFAP和S100染色检测到细胞核的分裂和固缩。波形蛋白、层粘连蛋白和GS的免疫染色也标记了这些星形胶质细胞,提示星形胶质细胞的免疫染色对于评估颅脑损伤后的早期脑损伤是有用的.脑损伤后少突胶质细胞的变化:脑损伤组少突胶质细胞经免疫组化染色,未标记对照组。因此,CNB染色对检测颅脑损伤后早期少突胶质细胞的变化非常有用.脑损伤后小胶质细胞的变化:在存活超过2周的脑损伤病例中,凝集素染色显示蓖麻凝集素-1(RCA 1)标记的所谓泡沫细胞,在存活超过9小时的病例中,凝集素染色显示肥大的小胶质细胞,因此RCA 1的凝集素染色可能有助于估计创伤后存活时间。
项目成果
期刊论文数量(4)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
M. Ogata: "Neuron-specific enolase as an effctive immunohistochemical marker for injured axons after fatal brain injury"International Journal of Legal Medicine. 113. 19-25 (1999)
M. Ogata:“神经元特异性烯醇化酶作为致命性脑损伤后受损轴突的有效免疫组织化学标记”《国际法律医学杂志》。
- DOI:
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- 影响因子:0
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M.ogata: "Internationnal journal of legal medicine"Neuron-specific enolase as an effective immunohistochemical makker for injured axons affer fatal brain injury. 19-25 (1999)
M.ogata:《国际法医学杂志》神经元特异性烯醇化酶作为有效的免疫组织化学标记物,可用于致命性脑损伤的受损轴突。
- DOI:
- 发表时间:
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- 影响因子:0
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Mamoru Ogata: "Neuron-specific enolase as an effective immunohistochemical marker for injured axons after fatal brain injury"International Journal of Legal Medicine. 113. 19-25 (1999)
Mamoru Ogata:“神经元特异性烯醇化酶作为致命性脑损伤后受损轴突的有效免疫组织化学标记”《国际法律医学杂志》。
- DOI:
- 发表时间:
- 期刊:
- 影响因子:0
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- 通讯作者:
M.Ogata: "Neuron-specific enolose as an effective immunohistochemical Marker for injured axons after fatal brain injury"Intaernatinal Jourmal of Legal Medicine. 113巻1号. 19-25 (1999)
M.Ogata:“神经元特异性烯醇化物作为致命性脑损伤后受损轴突的有效免疫组织化学标记”,《国际法律医学杂志》,第 113 卷,第 1. 19-25 期(1999 年)。
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{{ truncateString('OGATA Mamoru', 18)}}的其他基金
Investigation of postmortem differential diagnosis between traumatic and non-traumatic axonal injury
创伤性和非创伤性轴索损伤的死后鉴别诊断研究
- 批准号:
16K09212 - 财政年份:2016
- 资助金额:
$ 1.66万 - 项目类别:
Grant-in-Aid for Scientific Research (C)
Determination of the infiltration of neutrophils into organs resulting from repetitive injuries, and development of diagnostic methodsfor the physical abuse
确定因重复性损伤而导致的中性粒细胞浸润器官,并开发身体虐待的诊断方法
- 批准号:
22590638 - 财政年份:2010
- 资助金额:
$ 1.66万 - 项目类别:
Grant-in-Aid for Scientific Research (C)
Study on Forensic Pathological Demonstration of Child, Partner and Elder Abuse
虐待儿童、伴侣和老人的法医病理学论证研究
- 批准号:
19590677 - 财政年份:2007
- 资助金额:
$ 1.66万 - 项目类别:
Grant-in-Aid for Scientific Research (C)
Study on differential diagnosis of traumatic or intrinsic cerebral hematoma of the basal nucleus by use of immunohistochemical markers of blood vessels
血管免疫组化标记物鉴别诊断外伤性或内源性基底核血肿的研究
- 批准号:
17590581 - 财政年份:2005
- 资助金额:
$ 1.66万 - 项目类别:
Grant-in-Aid for Scientific Research (C)
Immunohistochemical syudy on differential diagnosis of traumatic or intrinsic cerebral hematoma
外伤性或内源性脑血肿鉴别诊断的免疫组化研究
- 批准号:
14570390 - 财政年份:2002
- 资助金额:
$ 1.66万 - 项目类别:
Grant-in-Aid for Scientific Research (C)
Determination of cause of death and estimation of survival period by the use of immunohistochemical markers of glial cells
利用神经胶质细胞的免疫组织化学标记物确定死亡原因并估计生存期
- 批准号:
12670398 - 财政年份:2000
- 资助金额:
$ 1.66万 - 项目类别:
Grant-in-Aid for Scientific Research (C)
Immunohistochemical studies on changes of the components of the nervous system after head injury and their application to estimating the duration of posttraumatic survival.
头部损伤后神经系统组成变化的免疫组织化学研究及其在估计创伤后生存持续时间中的应用。
- 批准号:
08670494 - 财政年份:1996
- 资助金额:
$ 1.66万 - 项目类别:
Grant-in-Aid for Scientific Research (C)
Studies on morphological changes of the nerve fibers (axon and myelin) after head injury.
头部损伤后神经纤维(轴突和髓磷脂)形态变化的研究。
- 批准号:
06670463 - 财政年份:1994
- 资助金额:
$ 1.66万 - 项目类别:
Grant-in-Aid for General Scientific Research (C)
Studies on DNA extracted from postmortem tissues
从死后组织中提取DNA的研究
- 批准号:
04670359 - 财政年份:1992
- 资助金额:
$ 1.66万 - 项目类别:
Grant-in-Aid for General Scientific Research (C)
相似海外基金
Molecular Mechanisms and Treatment of Diffuse Axonal Injury
弥漫性轴突损伤的分子机制和治疗
- 批准号:
10727616 - 财政年份:2022
- 资助金额:
$ 1.66万 - 项目类别:
Molecular Mechanisms and Treatment of Diffuse Axonal Injury
弥漫性轴突损伤的分子机制和治疗
- 批准号:
9892622 - 财政年份:2019
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$ 1.66万 - 项目类别:
Molecular Mechanisms and Treatment of Diffuse Axonal Injury
弥漫性轴突损伤的分子机制和治疗
- 批准号:
10248498 - 财政年份:2019
- 资助金额:
$ 1.66万 - 项目类别:
Molecular Mechanisms and Treatment of Diffuse Axonal Injury
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- 批准号:
10023949 - 财政年份:2019
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$ 1.66万 - 项目类别:
Tau protein as a diagnostic biomarker for diffuse axonal injury
Tau 蛋白作为弥漫性轴突损伤的诊断生物标志物
- 批准号:
15K20334 - 财政年份:2015
- 资助金额:
$ 1.66万 - 项目类别:
Grant-in-Aid for Young Scientists (B)
Evaluation of functional disorder of nerve cells with direction controlled axons for the prediction of Diffuse Axonal Injury (DAI)
评估具有方向控制轴突的神经细胞功能障碍以预测弥漫性轴突损伤 (DAI)
- 批准号:
25289064 - 财政年份:2013
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$ 1.66万 - 项目类别:
Grant-in-Aid for Scientific Research (B)
Successive changes of invisible brain injury, cognitive disorders, and activities of daily living in patients with diffuse axonal injury
弥漫性轴突损伤患者隐性脑损伤、认知障碍及日常生活活动的连续变化
- 批准号:
24700518 - 财政年份:2012
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$ 1.66万 - 项目类别:
Grant-in-Aid for Young Scientists (B)
Symptomatology of focal brain injury and diffuse axonal injury, by applying diffuse tensor imaging
应用弥散张量成像研究局灶性脑损伤和弥漫性轴突损伤的症状
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23791328 - 财政年份:2011
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$ 1.66万 - 项目类别:
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$ 1.66万 - 项目类别:
NHMRC Project Grants
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21700520 - 财政年份:2009
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