Background:Traumatic brain injury,one of the leading causes of death in adults under 40 years of age in the world,is frequently caused by mechanical shock,resulting in diffuse neuronal damage and long-term cognitive d...Background:Traumatic brain injury,one of the leading causes of death in adults under 40 years of age in the world,is frequently caused by mechanical shock,resulting in diffuse neuronal damage and long-term cognitive dysfunction.Many existing TBI animal models revival with expensive equipment or special room are needed or the processes of operations are complex and not easy to be widely used.Therefore,a simpler TBI model needs to be designed.Methods:Our TBI model is an innovation of the modeling method through air guns shutting rubber bullets.A core facet is the application of our designed rubber bullet impact device.It could focus the hitting power to the fixed site of the brain,thus triggering a mild closed head injury.Moreover,the degree of damage can be adjusted by the times of shots.Results:Our model induced blood-brain barrier leakage and diffused neuronal damage.Besides,it led to an increased level of Tau phosphorylation and resulted in cognitive dysfunction within several weeks post-injury.Conclusion:Our TBI model is not only simple and time-saving but also can simulate mild brain injuries in clinical.It is suitable for exploring pathobiological mechanisms as well as a screening of potential therapies for TBI.展开更多
Previous studies of integrin αvβ3 have focused on ischemic brain damage, although the role of integrin αvβ3 in ischemic preconditioning （IP） has rarely been reported. The present study analyzed the effects of IP...Previous studies of integrin αvβ3 have focused on ischemic brain damage, although the role of integrin αvβ3 in ischemic preconditioning （IP） has rarely been reported. The present study analyzed the effects of IP on integrin αvβ3 mRNA expression following cerebral ischemia through the use of hematoxylin-eosin staining and real-time quantitative polymerase chain reaction techniques. Integrin avid3 mRNA expression in the ischemia group peaked at 24 hours after ischemia-reperfusion. In the IP ＋ ischemia group, integrin αvβ3 mRNA expression increased after 24 hours, but remained significantly less than the ischemia group, and expression continued to increase until 7 days after ischemiaJreperfusion. These results demonstrate that IP effectively attenuated upregulation of integrin αvβ3 mRNA expression at 24 hours after ischemia.展开更多
基金This work was supported by the National Natural Science Foundation of China(grant number 81671264)Guangzhou Scientific Foundation Committee(grant numbers 201704020222 and 201807010094)
文摘Background:Traumatic brain injury,one of the leading causes of death in adults under 40 years of age in the world,is frequently caused by mechanical shock,resulting in diffuse neuronal damage and long-term cognitive dysfunction.Many existing TBI animal models revival with expensive equipment or special room are needed or the processes of operations are complex and not easy to be widely used.Therefore,a simpler TBI model needs to be designed.Methods:Our TBI model is an innovation of the modeling method through air guns shutting rubber bullets.A core facet is the application of our designed rubber bullet impact device.It could focus the hitting power to the fixed site of the brain,thus triggering a mild closed head injury.Moreover,the degree of damage can be adjusted by the times of shots.Results:Our model induced blood-brain barrier leakage and diffused neuronal damage.Besides,it led to an increased level of Tau phosphorylation and resulted in cognitive dysfunction within several weeks post-injury.Conclusion:Our TBI model is not only simple and time-saving but also can simulate mild brain injuries in clinical.It is suitable for exploring pathobiological mechanisms as well as a screening of potential therapies for TBI.
基金the National Natural Science Foundation of China,No. 30870849,81071068the Science and Technology Planning Project of Guangdong Province,No. 2009B030801101
文摘Previous studies of integrin αvβ3 have focused on ischemic brain damage, although the role of integrin αvβ3 in ischemic preconditioning （IP） has rarely been reported. The present study analyzed the effects of IP on integrin αvβ3 mRNA expression following cerebral ischemia through the use of hematoxylin-eosin staining and real-time quantitative polymerase chain reaction techniques. Integrin avid3 mRNA expression in the ischemia group peaked at 24 hours after ischemia-reperfusion. In the IP ＋ ischemia group, integrin αvβ3 mRNA expression increased after 24 hours, but remained significantly less than the ischemia group, and expression continued to increase until 7 days after ischemiaJreperfusion. These results demonstrate that IP effectively attenuated upregulation of integrin αvβ3 mRNA expression at 24 hours after ischemia.
