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Background::Posttraumatic stress disorder (PTSD) and depression are highly comorbid. Psilocybin exerts substantial therapeutic effects on depression by promoting neuroplasticity. Fear extinction is a key process in the mechanism of first-line exposure-based therapies for PTSD. We hypothesized that psilocybin would facilitate fear extinction by promoting hippocampal neuroplasticity.Methods::First, we assessed the effects of psilocybin on percentage of freezing time in an auditory cued fear conditioning (FC) and fear extinction paradigm in mice. Psilocybin was administered 30 min before extinction training. Fear extinction testing was performed on the first day; fear extinction retrieval and fear renewal were tested on the sixth and seventh days, respectively. Furthermore, we verified the effect of psilocybin on hippocampal neuroplasticity using Golgi staining for the dendritic complexity and spine density, Western blotting for the protein levels of brain derived neurotrophic factor (BDNF) and mechanistic targe

作者:Du Yingjie;Li Yunfeng;Zhao Xiangting;Yao Yishan;Wang Bin;Zhang Liming;Wang Guyan

来源:中华医学杂志英文版 2023 年 136卷 24期

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作者:
Du Yingjie;Li Yunfeng;Zhao Xiangting;Yao Yishan;Wang Bin;Zhang Liming;Wang Guyan
来源:
中华医学杂志英文版 2023 年 136卷 24期
标签:
Brain-derived neurotrophic factor Bromodeoxyuridine Depression Doublecortin domain proteins Extinction, psychological Freezing Hippocampus Neuronal plasticity Psilocybin Stress disorders, post-traumatic Brain-derived neurotrophic factor Bromodeoxyuridine Depression Doublecortin domain proteins Extinction, psychological Freezing Hippocampus Neuronal pl
Background::Posttraumatic stress disorder (PTSD) and depression are highly comorbid. Psilocybin exerts substantial therapeutic effects on depression by promoting neuroplasticity. Fear extinction is a key process in the mechanism of first-line exposure-based therapies for PTSD. We hypothesized that psilocybin would facilitate fear extinction by promoting hippocampal neuroplasticity.Methods::First, we assessed the effects of psilocybin on percentage of freezing time in an auditory cued fear conditioning (FC) and fear extinction paradigm in mice. Psilocybin was administered 30 min before extinction training. Fear extinction testing was performed on the first day; fear extinction retrieval and fear renewal were tested on the sixth and seventh days, respectively. Furthermore, we verified the effect of psilocybin on hippocampal neuroplasticity using Golgi staining for the dendritic complexity and spine density, Western blotting for the protein levels of brain derived neurotrophic factor (BDNF) and mechanistic targe

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