Association and histological characteristics of endplate injury and intervertebral disc degeneration in a rat model

医学 椎间盘 解剖 病理 椎体 H&E染色 免疫组织化学
作者
Qihang Su,Yongchao Li,Xiaofei Feng,Jun Tan,Heng’an Ge,Biao Cheng,Yan Zhang
出处
期刊:Injury-international Journal of The Care of The Injured [Elsevier BV]
卷期号:52 (8): 2084-2094 被引量:15
标识
DOI:10.1016/j.injury.2021.05.034
摘要

Introduction The purpose of this study was to construct a rat caudal vertebral body fracture model and to analyze the association and histological characteristics of vertebral body fracture with endplate injury and adjacent intervertebral disc degeneration. Materials and methods This study included 144 clean-grade male Sprague-Dawley rats, which were randomly divided into a control, middle vertebral body injury (MI), and endplate injury (EI) groups. A vertebral body fracture with or without endplate injury was developed by either drilling a hole in the middle of a rat caudal vertebral body to create a fracture with an intact endplate or drilling a hole in the vertebral body near the intervertebral disc to create a vertebral body fracture with endplate injury. The histological differences in the adjacent intervertebral discs of vertebral body fractures with or without endplate injury were detected using imaging, non-specific histological staining, immunohistochemistry and TUNEL assay. Results Imaging results revealed that the EI group showed a significant decrease in intervertebral space height and intervertebral disc T2 signal over time. Non-specific histological staining revealed that in the EI group, the intervertebral disc was degenerative. Immunohistochemistry indicated that Aggrecan and Collagen-II were decreased and inflammatory factors were increased in the EI group. The TUNEL detection found that apoptosis was significantly increased in the EI group as compared with the MI and control groups. Conclusion In rat caudal vertebral body fractures, a fracture with endplate injury is more likely to induce or accelerate degeneration of adjacent intervertebral discs.
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
充电宝应助voifhpg采纳,获得10
刚刚
原子发布了新的文献求助10
刚刚
sdl发布了新的文献求助10
1秒前
Uuchandesu应助背后的小白菜采纳,获得10
6秒前
原子完成签到,获得积分10
6秒前
7秒前
月光入梦完成签到 ,获得积分10
7秒前
suiyi完成签到,获得积分10
7秒前
hkh发布了新的文献求助10
7秒前
sunflowers发布了新的文献求助20
8秒前
jianjiao完成签到,获得积分10
8秒前
茶多酚完成签到,获得积分10
9秒前
lu完成签到,获得积分10
9秒前
古琴残梦发布了新的文献求助10
10秒前
lxy发布了新的文献求助10
11秒前
Shawn完成签到,获得积分10
14秒前
17秒前
17秒前
vivianzhang完成签到,获得积分10
18秒前
xiaoz完成签到,获得积分10
24秒前
银杏发布了新的文献求助20
25秒前
26秒前
活力寄凡完成签到,获得积分10
30秒前
曾经饼干发布了新的文献求助10
30秒前
31秒前
丘比特应助Echo采纳,获得10
31秒前
32秒前
kingripple发布了新的文献求助10
33秒前
小小狗完成签到,获得积分10
33秒前
35秒前
Rita应助Tzzl0226采纳,获得10
36秒前
一一完成签到 ,获得积分10
37秒前
研友_LpvQlZ完成签到,获得积分10
38秒前
陈莹发布了新的文献求助10
38秒前
38秒前
41秒前
毓香谷的春天完成签到 ,获得积分0
41秒前
mss12138完成签到,获得积分10
41秒前
42秒前
voifhpg发布了新的文献求助10
42秒前
高分求助中
【此为提示信息,请勿应助】请按要求发布求助,避免被关 20000
ISCN 2024 – An International System for Human Cytogenomic Nomenclature (2024) 3000
Continuum Thermodynamics and Material Modelling 2000
Encyclopedia of Geology (2nd Edition) 2000
105th Edition CRC Handbook of Chemistry and Physics 1600
Izeltabart tapatansine - AdisInsight 800
Maneuvering of a Damaged Navy Combatant 650
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 有机化学 物理 生物化学 纳米技术 计算机科学 化学工程 内科学 复合材料 物理化学 电极 遗传学 量子力学 基因 冶金 催化作用
热门帖子
关注 科研通微信公众号,转发送积分 3774441
求助须知:如何正确求助?哪些是违规求助? 3320155
关于积分的说明 10198712
捐赠科研通 3034786
什么是DOI,文献DOI怎么找? 1665211
邀请新用户注册赠送积分活动 796703
科研通“疑难数据库(出版商)”最低求助积分说明 757552