Stab-Wound Mouse Model for Studying Hemorrhage and Inflammation in Traumatic Brain Injury

创伤性脑损伤 医学 刺伤 炎症 爆炸伤 薄壁组织 病变 毒物控制 病理 外科 免疫学 医疗急救 精神科
作者
Kei Hashimoto,Mari Nakashima,Yasunori Miyamoto,Hiroko Ikeshima‐Kataoka
出处
期刊:Journal of Visualized Experiments [MyJoVE Corporation]
卷期号: (216) 被引量:1
标识
DOI:10.3791/67797
摘要

Traumatic brain injury (TBI) results from physical damage, often caused by accidents or sports-related incidents. The causes of TBI are diverse, including concussions, brain contusions, hematomas, and skull fractures. To replicate these different causes, various TBI mouse models have been developed using distinct protocols. Physical brain injury leads to both primary and secondary brain injuries, which exacerbate neuronal loss. Primary injury occurs immediately after the damage, often due to hemorrhage, and subsequently triggers secondary injuries, including inflammation around the lesion. Developing a TBI model suitable for assessing hemorrhage extension and inflammatory severity is therefore crucial. This protocol introduces a method for mimicking penetrating brain injury, referred to as the stab-wound TBI mouse model, to study mechanisms of hemorrhage, inflammation, and neuronal loss associated with TBI pathology. This model is created by puncturing the skull and brain with needles and is simple to execute without the need for specialized experimental equipment. Additionally, the minor injury inflicted on the mouse cerebral cortex using a needle does not affect the animal's behavior post-surgery. This feature allows researchers to study the localized effects of brain injury without concerns about broader behavioral consequences. Sample data from stab-wounded mouse cerebral cortices demonstrate the model's effectiveness in assessing blood leakage into the parenchyma, glial activation, and inflammatory cytokine production. Furthermore, this protocol facilitates the evaluation of blood coagulants and anti-inflammatory compounds, aiding in the development of therapeutic agents for TBI.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
刚刚
善良的樱完成签到 ,获得积分10
刚刚
哈哈哈哈发布了新的文献求助30
1秒前
2秒前
2秒前
梨涡MAMA发布了新的文献求助30
3秒前
图灵桑发布了新的文献求助10
3秒前
激情的又菡完成签到 ,获得积分10
4秒前
lancer发布了新的文献求助50
4秒前
长镜头完成签到 ,获得积分10
5秒前
岁月静好完成签到,获得积分10
5秒前
6秒前
6秒前
近代发布了新的文献求助10
7秒前
1111发布了新的文献求助10
7秒前
yu发布了新的文献求助10
8秒前
仁爱的伯云完成签到,获得积分0
9秒前
顾矜应助撒西不理采纳,获得10
10秒前
11秒前
白雅方完成签到,获得积分10
11秒前
昔我往矣发布了新的文献求助10
12秒前
12秒前
12秒前
研友_VZG7GZ应助阔达宛凝采纳,获得10
12秒前
今后应助yu采纳,获得10
13秒前
科研通AI6.1应助HY采纳,获得10
13秒前
14秒前
赘婿应助要减肥的胖子采纳,获得10
15秒前
笑点低忆之完成签到 ,获得积分10
15秒前
17秒前
agrlook发布了新的文献求助10
17秒前
田园发布了新的文献求助10
17秒前
20秒前
21秒前
21秒前
22秒前
bk发布了新的文献求助10
23秒前
25秒前
wjwww发布了新的文献求助10
25秒前
小二郎应助善良安荷采纳,获得10
25秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Modern Epidemiology, Fourth Edition 5000
Digital Twins of Advanced Materials Processing 2000
Weaponeering, Fourth Edition – Two Volume SET 2000
Polymorphism and polytypism in crystals 1000
Social Cognition: Understanding People and Events 800
Signals, Systems, and Signal Processing 610
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 纳米技术 有机化学 物理 生物化学 化学工程 计算机科学 复合材料 内科学 催化作用 光电子学 物理化学 电极 冶金 遗传学 细胞生物学
热门帖子
关注 科研通微信公众号,转发送积分 6025410
求助须知:如何正确求助?哪些是违规求助? 7662675
关于积分的说明 16179208
捐赠科研通 5173549
什么是DOI,文献DOI怎么找? 2768262
邀请新用户注册赠送积分活动 1751639
关于科研通互助平台的介绍 1637724