Abstract | AIMS: METHODS: Fear memory extinction was examined in PTSD mice model. Thirty-six mice were randomly divided into three groups: a shock + propofol group (sh + Pro), shock + normal saline group (sh + NS), and sham group. The mice were treated with propofol (150 mg/kg) or normal saline (of the same volume) intraperitoneally 30 min after the conditioning. These mice's behavior was analysed with contextual test, sucrose preference test (SPT) and Morris water maze (MWM). Additionally, the synaptic plasticity of the hippocampus was examined by long-term potentiation (LTP) and long-term depression (LTD). KEY FINDINGS: Compared with the sham group, the sh + NS group showed increased freezing time and depressive behavior, meanwhile the sh + Pro group showed minor behavioral changes. What's more, we found that propofol rescued the impaired long-term potentiation (LTP) and long-term depression (LTD) in hippocampus of PTSD mice. All these suggest that propofol can accelerate fear memory extinction and change synaptic plasticity of PTSD mice. SIGNIFICANCE: The study proved that propofol can protect the mice from PTSD by reserving synaptic plasticity and brought a new insight into PTSD treatment indicating that propofol maybe a potential cure for PTSD.
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Authors | Wanqiu Niu, Yanhong Duan, Yu Kang, Xiaohua Cao, Qingsheng Xue |
Journal | Life sciences
(Life Sci)
Vol. 293
Pg. 120349
(Mar 15 2022)
ISSN: 1879-0631 [Electronic] Netherlands |
PMID | 35065162
(Publication Type: Journal Article)
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Copyright | Copyright © 2022 The Authors. Published by Elsevier Inc. All rights reserved. |
Chemical References |
- Hypnotics and Sedatives
- Propofol
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Topics |
- Animals
- Hippocampus
(drug effects, physiology)
- Hypnotics and Sedatives
(pharmacology, therapeutic use)
- Long-Term Potentiation
(drug effects, physiology)
- Male
- Maze Learning
(drug effects, physiology)
- Memory
(drug effects, physiology)
- Mice
- Mice, Inbred C57BL
- Neuronal Plasticity
(drug effects, physiology)
- Propofol
(pharmacology, therapeutic use)
- Stress Disorders, Post-Traumatic
(drug therapy, physiopathology, psychology)
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