Relationship between Expression Changes of CB2R and Wound Age of Brain Contusion in Mice.
10.12116/j.issn.1004-5619.2019.02.002
- Author:
Jing-wei CHEN
1
;
Peng-fei WANG
1
;
Meng-zhou ZHANG
1
;
Zhong-duo ZHANG
1
;
Hao CHENG
1
;
Ying-fu SUN
1
;
Shu-heng WEN
1
;
Xiang-shen GUO
1
;
Rui ZHAO
1
;
Da-wei GUAN
1
Author Information
1. Center of Medico-legal Investigation, School of Forensic Medicine, China Medical University, Shenyang 110122, China.
- Publication Type:Journal Article
- Keywords:
forensic pathology;
brain injuries;
immunohistochemistry staining;
immunofluorescence technique;
blotting, Western;
cannabinoid type 2 receptor;
wound age estimation;
mice
- MeSH:
Animals;
Blotting, Western;
Brain Contusion/metabolism*;
Brain Injuries;
Forensic Pathology;
Mice;
Muscle, Skeletal/pathology*;
Receptor, Cannabinoid, CB2/metabolism*;
Receptors, Cannabinoid;
Time Factors;
Wound Healing/physiology*
- From:
Journal of Forensic Medicine
2019;35(2):136-142
- CountryChina
- Language:English
-
Abstract:
Objective To investigate the expression of cannabinoid type 2 receptor （CB2R） at different time points after brain contusion and its relationship with wound age of mice. Methods A mouse brain contusion model was established with PCI3000 Precision Cortical Impactor. Expression changes of CB2R around the injured area were detected with immunohistochemical staining, immunofluorescent staining and Western blotting at different time points. Results Immunohistochemical staining results showed that only a few cells in the cerebral cortex of the sham operated group had CB2R positive expression. The ratio of CB2R positive cells gradually increased after injury and reached the peak twice at 12 h and 7 d post-injury, followed by a decrease to the normal level 28 d post-injury. The results of Western blotting were consistent with the immunohistochemical staining results. Immunofluorescent staining demonstrated that the changes of the ratio of CB2R positive cells in neurons, CB2R positive cells in monocytes and CB2R positive cells in astrocytes to the total cell number showed a single peak pattern, which peaked at 12 h, 1 d and 7 d post-injury, respectively. Conclusion The expression of CB2R after brain contusion in neurons, monocytes and astrocytes in mice suggests that it is likely to be involved in the regulation of the biological functions of those cells. The changes in CB2R are time-dependent, which suggests its potential applicability as a biological indicator for wound age estimation of brain contusion in forensic practice.
