A Mouse Model of Neurodegeneration Induced by Blade Penetrating Stab Wound to the Hippocampus.
Bao-Dong HeChang-Mei LiuZhao-Qian TengPublished in: Biology (2022)
Traumatic brain injury (TBI) is closely associated with the later development of neurodegenerative and psychiatric diseases which are still incurable. Although various animal TBI models have been generated, they usually have weaknesses in standardization, survivability and/or reproducibility. In the present study, we investigated whether applying a blade penetrating stab wound to the hippocampus would create an animal model of cognitive deficits. Open-field, Morris water maze and Barnes maze tests were used to evaluate the animal behaviors. The immunofluorescence staining of NeuN, GFAP, IBA1, and TUNEL was conducted to analyze the changes in neurons, astrocytes, and microglia, as well as cell death. Mice with a hippocampal blade stab injury (HBSI) displayed the activation of microglia and astrocytes, inflammation, neuronal apoptosis, and deficits in spatial learning and memory. These findings suggest that HBSI is an easy approach to generate a reliable in vivo model of TBI to capture hemorrhage, neuroinflammation, reactive gliosis, and neural death, as well as cognitive deficits observed in human patients.
Keyphrases
- traumatic brain injury
- cell death
- cerebral ischemia
- end stage renal disease
- mouse model
- oxidative stress
- severe traumatic brain injury
- inflammatory response
- chronic kidney disease
- ejection fraction
- cell cycle arrest
- endothelial cells
- peritoneal dialysis
- neuropathic pain
- prognostic factors
- cognitive impairment
- minimally invasive
- type diabetes
- endoplasmic reticulum stress
- subarachnoid hemorrhage
- brain injury
- blood brain barrier
- prefrontal cortex
- surgical site infection
- insulin resistance
- patient reported
- metabolic syndrome
- cell proliferation
- single molecule