• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

βAPP 免疫组织化学法检测道路交通事故致颅脑损伤的快速死亡中的轴索损伤。

Axonal injury is detected by βAPP immunohistochemistry in rapid death from head injury following road traffic collision.

机构信息

Department of Clinical Neuropathology, King's College Hospital NHS Foundation Trust, London, UK.

London Neurodegenerative Diseases Brain Bank, Basic and Clinical Neuroscience Department, Institute of Psychiatry, Psychology and Neuroscience, King's College London, London, UK.

出版信息

Int J Legal Med. 2022 Sep;136(5):1321-1339. doi: 10.1007/s00414-022-02807-z. Epub 2022 Apr 30.

DOI:10.1007/s00414-022-02807-z
PMID:35488928
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9375765/
Abstract

The accumulation of βAPP caused by axonal injury is an active energy-dependent process thought to require blood circulation; therefore, it is closely related to the post-injury survival time. Currently, the earliest reported time at which axonal injury can be detected in post-mortem traumatic brain injury (TBI) tissue by βAPP (Beta Amyloid Precursor Protein) immunohistochemistry is 35 min. The aim of this study is to investigate whether βAPP staining for axonal injury can be detected in patients who died rapidly after TBI in road traffic collision (RTC), in a period of less than 30 min.We retrospectively studied thirty-seven patients (group 1) died very rapidly at the scene; evidenced by forensic assessment of injuries short survival, four patients died after a survival period of between 31 min and 12 h (group 2) and eight patients between 2 and 31 days (group 3). The brains were comprehensively examined and sampled at the time of the autopsy, and βAPP immunohistochemistry carried out on sections from a number of brain areas.βAPP immunoreactivity was demonstrated in 35/37 brains in group 1, albeit with a low frequency and in a variable pattern, and with more intensity and frequency in all brains of group 2 and 7/8 brains from group 3, compared with no similar βAPP immunoreactivity in the control group. The results suggest axonal injury can be detected in those who died rapidly after RTC in a period of less than 30 min, which can help in the diagnosis of severe TBI with short survival time.

摘要

βAPP 的积累是由轴索损伤引起的,这是一个主动的能量依赖过程,被认为需要血液循环;因此,它与损伤后的存活时间密切相关。目前,通过βAPP(β淀粉样前体蛋白)免疫组化在死后创伤性脑损伤(TBI)组织中检测到轴索损伤的最早报道时间为 35 分钟。本研究旨在探讨βAPP 染色是否可以检测到在道路交通碰撞(RTC)中迅速死亡的 TBI 患者的轴索损伤,时间少于 30 分钟。我们回顾性研究了 37 例(组 1)非常迅速地在现场死亡的患者;根据损伤的法医学评估,存活时间短,4 例患者在 31 分钟至 12 小时之间(组 2)和 8 例患者在 2 至 31 天之间(组 3)死亡。在尸检时对大脑进行了全面检查和取样,并对来自多个脑区的切片进行了βAPP 免疫组织化学染色。在组 1 的 37 例脑中有 35 例显示βAPP 免疫反应性,尽管频率较低,模式不同,但组 2 和组 3 的所有脑中有更多的强度和频率,对照组没有类似的βAPP 免疫反应性。结果表明,在 RTC 后迅速死亡的患者中,在 30 分钟内可以检测到轴索损伤,这有助于诊断存活时间短的严重 TBI。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/55b4/9375765/81f203e3e97d/414_2022_2807_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/55b4/9375765/edab103711da/414_2022_2807_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/55b4/9375765/4e0f6da28612/414_2022_2807_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/55b4/9375765/cfc154ba90be/414_2022_2807_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/55b4/9375765/8d7304323b31/414_2022_2807_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/55b4/9375765/81f203e3e97d/414_2022_2807_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/55b4/9375765/edab103711da/414_2022_2807_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/55b4/9375765/4e0f6da28612/414_2022_2807_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/55b4/9375765/cfc154ba90be/414_2022_2807_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/55b4/9375765/8d7304323b31/414_2022_2807_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/55b4/9375765/81f203e3e97d/414_2022_2807_Fig5_HTML.jpg

相似文献

1
Axonal injury is detected by βAPP immunohistochemistry in rapid death from head injury following road traffic collision.βAPP 免疫组织化学法检测道路交通事故致颅脑损伤的快速死亡中的轴索损伤。
Int J Legal Med. 2022 Sep;136(5):1321-1339. doi: 10.1007/s00414-022-02807-z. Epub 2022 Apr 30.
2
Beta-amyloid precursor protein staining of nonaccidental central nervous system injury in pediatric autopsies.小儿尸检中非意外性中枢神经系统损伤的β-淀粉样前体蛋白染色
J Neurotrauma. 2003 Apr;20(4):347-55. doi: 10.1089/089771503765172309.
3
Trials and tribulations of using beta-amyloid precursor protein immunohistochemistry to evaluate traumatic brain injury in adults.使用β-淀粉样前体蛋白免疫组织化学评估成人创伤性脑损伤的试验与磨难
Forensic Sci Int. 2004 Dec 16;146(2-3):89-96. doi: 10.1016/S0379-0738(03)00274-3.
4
Beta-amyloid precursor protein immunohistochemistry in the evaluation of pediatric traumatic optic nerve injury.β-淀粉样前体蛋白免疫组化在小儿外伤性视神经损伤评估中的应用
Ophthalmology. 2004 Apr;111(4):822-7. doi: 10.1016/j.ophtha.2003.07.016.
5
Correlation of survival time with size of axonal swellings in diffuse axonal injury.弥漫性轴索损伤中生存时间与轴突肿胀大小的相关性。
Acta Neuropathol. 1999 Aug;98(2):197-202. doi: 10.1007/s004010051069.
6
Traumatic axonal damage in the brain can be detected using beta-APP immunohistochemistry within 35 min after head injury to human adults.对于成年人类,头部受伤后35分钟内,可使用β-淀粉样前体蛋白免疫组织化学法检测脑内的创伤性轴突损伤。
Neuropathol Appl Neurobiol. 2007 Apr;33(2):226-37. doi: 10.1111/j.1365-2990.2006.00794.x.
7
Immunomorphological sequelae of severe brain injury induced by fluid-percussion in juvenile pigs--effects of mild hypothermia.幼猪液压冲击致重度脑损伤的免疫形态学后遗症——轻度低温的影响
Acta Neuropathol. 2001 May;101(5):424-34. doi: 10.1007/s004010000290.
8
Brain damage and axonal injury in a Scottish cohort of neonatal deaths.苏格兰新生儿死亡队列中的脑损伤和轴突损伤
Brain. 2005 May;128(Pt 5):1070-81. doi: 10.1093/brain/awh436. Epub 2005 Feb 10.
9
SNTF immunostaining reveals previously undetected axonal pathology in traumatic brain injury.SNTF免疫染色揭示了创伤性脑损伤中先前未被检测到的轴突病理学特征。
Acta Neuropathol. 2016 Jan;131(1):115-35. doi: 10.1007/s00401-015-1506-0. Epub 2015 Nov 20.
10
Two patterns of beta-amyloid precursor protein (APP) immunoreactivity in cases of blunt head injury.钝器头部损伤病例中β-淀粉样前体蛋白(APP)免疫反应性的两种模式。
Leg Med (Tokyo). 2009 Apr;11 Suppl 1:S171-3. doi: 10.1016/j.legalmed.2009.01.076. Epub 2009 Feb 28.

引用本文的文献

1
Comparison of background characteristics and neuropathology findings between medico-legal autopsy cases with traumatic axonal injury, vascular axonal injury, or absence of axonal injury in β-amyloid precursor protein stain.在β-淀粉样前体蛋白染色中,对有创伤性轴突损伤、血管性轴突损伤或无轴突损伤的法医尸检病例的背景特征和神经病理学发现进行比较。
Int J Legal Med. 2025 May;139(3):1335-1342. doi: 10.1007/s00414-025-03415-3. Epub 2025 Jan 21.
2
Expression of RIPK-1 and S-100B in traumatic brain injury- exploring a forensic cases series.RIPK-1和S-100B在创伤性脑损伤中的表达——对一系列法医案例的研究
Int J Legal Med. 2025 May;139(3):1105-1112. doi: 10.1007/s00414-024-03400-2. Epub 2024 Dec 16.
3

本文引用的文献

1
Clusterin expression is upregulated following acute head injury and localizes to astrocytes in old head injury.簇集素表达在急性头部损伤后上调,并在陈旧性头部损伤中定位于星形胶质细胞。
Neuropathology. 2017 Feb;37(1):12-24. doi: 10.1111/neup.12320. Epub 2016 Jul 1.
2
Traumatic Axonal Injury: Mechanisms and Translational Opportunities.创伤性轴索损伤:机制与转化机遇
Trends Neurosci. 2016 May;39(5):311-324. doi: 10.1016/j.tins.2016.03.002. Epub 2016 Mar 31.
3
The neuroinflammatory response in humans after traumatic brain injury.创伤性脑损伤后人类的神经炎症反应。
A role for immunohistochemical stains in perinatal brain autopsies.
免疫组织化学染色在围产期脑尸检中的作用。
J Neuropathol Exp Neurol. 2024 Apr 19;83(5):345-356. doi: 10.1093/jnen/nlae019.
4
The Labyrinthine Landscape of APP Processing: State of the Art and Possible Novel Soluble APP-Related Molecular Players in Traumatic Brain Injury and Neurodegeneration.淀粉样前体蛋白(APP)加工的错综复杂景观:创伤性脑损伤和神经退行性变中最新的可溶性 APP 相关分子的可能新靶点。
Int J Mol Sci. 2023 Apr 2;24(7):6639. doi: 10.3390/ijms24076639.
5
Role of integrin and its potential as a novel postmortem biomarker in traumatic axonal injury.整合素的作用及其作为创伤性轴索损伤新型死后生物标志物的潜力。
Int J Legal Med. 2023 May;137(3):843-849. doi: 10.1007/s00414-022-02938-3. Epub 2022 Dec 23.
Neuropathol Appl Neurobiol. 2013 Oct;39(6):654-66. doi: 10.1111/nan.12008.
4
Axonal pathology in traumatic brain injury.创伤性脑损伤中的轴突病变。
Exp Neurol. 2013 Aug;246:35-43. doi: 10.1016/j.expneurol.2012.01.013. Epub 2012 Jan 20.
5
Cytokines and innate inflammation in the pathogenesis of human traumatic brain injury.细胞因子与固有炎症在人类创伤性脑损伤发病机制中的作用。
Prog Neurobiol. 2011 Nov;95(3):352-72. doi: 10.1016/j.pneurobio.2011.09.003. Epub 2011 Sep 16.
6
Biomarkers associated with diffuse traumatic axonal injury: exploring pathogenesis, early diagnosis, and prognosis.与弥漫性创伤性轴索损伤相关的生物标志物:探索发病机制、早期诊断及预后
J Trauma. 2010 Dec;69(6):1610-8. doi: 10.1097/TA.0b013e3181f5a9ed.
7
Clinical characteristics and pathophysiological mechanisms of focal and diffuse traumatic brain injury.局灶性和弥漫性创伤性脑损伤的临床特征和病理生理学机制。
J Cell Mol Med. 2010 Oct;14(10):2381-92. doi: 10.1111/j.1582-4934.2010.01164.x.
8
Mechanical breaking of microtubules in axons during dynamic stretch injury underlies delayed elasticity, microtubule disassembly, and axon degeneration.在动态拉伸损伤过程中,轴突中的微管机械断裂是延迟弹性、微管解体和轴突退化的基础。
FASEB J. 2010 May;24(5):1401-10. doi: 10.1096/fj.09-142844. Epub 2009 Dec 17.
9
Clusterin: a forgotten player in Alzheimer's disease.聚集素:阿尔茨海默病中被遗忘的角色。
Brain Res Rev. 2009 Oct;61(2):89-104. doi: 10.1016/j.brainresrev.2009.05.007. Epub 2009 Aug 3.
10
A lack of amyloid beta plaques despite persistent accumulation of amyloid beta in axons of long-term survivors of traumatic brain injury.尽管创伤性脑损伤长期幸存者的轴突中β淀粉样蛋白持续积累,但却缺乏β淀粉样蛋白斑块。
Brain Pathol. 2009 Apr;19(2):214-23. doi: 10.1111/j.1750-3639.2008.00176.x. Epub 2008 May 19.