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Long-lasting neurobehavioral alterations in burn-injured mice resembling post-traumatic stress disorder in humans.
Zhang, Qing-Hong; Hao, Ji-Wei; Li, Guang-Lei; Ji, Xiao-Jing; Zhou, Min; Yao, Yong-Ming.
Affiliation
  • Zhang QH; Trauma Research Center, Fourth Medical Center of Chinese PLA General Hospital, Beijing 100048, PR China. Electronic address: z_qinghong@aliyun.com.
  • Hao JW; Trauma Research Center, Fourth Medical Center of Chinese PLA General Hospital, Beijing 100048, PR China.
  • Li GL; Trauma Research Center, Fourth Medical Center of Chinese PLA General Hospital, Beijing 100048, PR China.
  • Ji XJ; Trauma Research Center, Fourth Medical Center of Chinese PLA General Hospital, Beijing 100048, PR China; Department of Emergency, First Hospital Affiliated to Wenzhou Medical College, Wenzhou, Zhejiang 325000, PR China.
  • Zhou M; Neurocritical Care Unit, The First Affiliated Hospital of USTC, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, Anhui 230001, PR China.
  • Yao YM; Trauma Research Center, Fourth Medical Center of Chinese PLA General Hospital, Beijing 100048, PR China.
Exp Neurol ; 323: 113084, 2020 01.
Article in En | MEDLINE | ID: mdl-31697945
OBJECTIVE: To establish an animal model for posttraumatic stress disorder in burn-injured patients. METHODS: Thermal-injured mice with 15% total body surface area were subjected to a series of neurobehavioral tests at 1 and 3 months postburn. Brains were collected for analysis of key molecules expression, spleens for T cell function analysis, and blood for biochemistry and hormones detection. RESULTS: Comparison with sham mice, burn mice showed extremely high locomotion in homecage, open field, and forced swimming tests, indicating a hyper-arousal state. Burn mice exhibited improved spatial memory in Morris Water Maze test and heightened context fear memory in context fear conditioning, suggesting re-experiencing behavior. Although burn mice showed pronounced passive avoidance in the step-through test, their active avoidance capability in response to the conditional stimulus in the shuttle box test was relatively deteriorated. Likewise, the retention of cue-feared memory was impaired in fear conditioning test. The above negative alterations in mood were recapitulated in open-field test, in which the burn mice displayed an anxiety-like behavior with less time spent in the center. However, no sign of depression was found in the forced swimming and sucrose preference tests. The negative mood of burn mice was reinforced by a deficit in sociality and preference for social novelty in social interaction test. These neurobehavioral alterations were associated with an increased expression of brain-derived neurotrophic factor along with a remarkable microgliosis and a moderate astrocytosis in the brain of burn vs. sham mice. Moreover, a prominent Th2 switch and consequent increased nuclear NF-κB translocation were seen in the splenic T cells from burn relative to sham mice. CONCLUSIONS: We conclude that even mild burn injury could lead to long-lasting cognitive and effective alterations in mice. These findings shed light on the interactions among neuropsychology, neurobiology, and immunology throughout the recovery period of burn injury.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Stress Disorders, Post-Traumatic / Behavior, Animal / Burns / Disease Models, Animal Type of study: Etiology_studies / Prognostic_studies Limits: Animals / Humans / Male Language: En Journal: Exp Neurol Year: 2020 Document type: Article Country of publication: Estados Unidos

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Stress Disorders, Post-Traumatic / Behavior, Animal / Burns / Disease Models, Animal Type of study: Etiology_studies / Prognostic_studies Limits: Animals / Humans / Male Language: En Journal: Exp Neurol Year: 2020 Document type: Article Country of publication: Estados Unidos