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作 者:佟雷[1] 季丽莉[1] 彭军波[1] 富长海[1] 王振宇[1]
机构地区:[1]中国医科大学基础医学院解剖学教研室,辽宁沈阳110122
出 处:《解剖科学进展》2017年第2期140-143,共4页Progress of Anatomical Sciences
基 金:辽宁省自然科学基金(2015020459;201602825)
摘 要:目的探讨腹腔注射Sigma-1受体激动剂PRE-084对创伤后应激障碍(PTSD)大鼠额叶神经元损伤的影响。方法利用单程长时应激(SPS)制备PTSD大鼠模型,将PTSD大鼠分为4组:vehicle、PRE-084、SPS+vehicle和SPS+PRE-084组;连续注射PRE-084 7d后,取材各组大鼠额叶,利用免疫荧光染色检测各组大鼠额叶Neu N表达情况,免疫荧光染色、Western blot检测p-ERK蛋白表达情况。结果免疫荧光染色结果显示,PTSD大鼠额叶神经元数量降低,腹腔注射PRE-084可以显著改善PTSD引起的神经元损伤;Western blot结果显示,PTSD大鼠额叶p-ERK表达水平降低,PRE-084可以显著升高p-ERK蛋白水平。结论腹腔注射Sigma-1受体激动剂PRE-084改善PTSD大鼠额叶神经元损伤可能与上调ERK信号通路相关。Objective To investigate the effect of Sigma-1 receptor agonist(PRE-084)on damaged neurons in prefrontal cortex of post-traumatic stress disorder(PTSD) rats. Methods The PTSD model was established by single prolonged stress paradigm(SPS). The animals were divided into 4 groups: vehicle, PRE-084, SPS+ vehicle and SPS+ PRE-084 group. The expression of Neu N in prefrontal cortex of rats was detected by immunofluorescence staining. The expression of p-ERK protein was detected by immunofluorescence staining and Western blot respectively. Results The percentage of Neu N positive cells in prefrontal cortex of SPS rats was decreased, and PRE-084 upregulated the number of Neu N positive cells. The expression level of p-ERK in prefrontal cortex was decreased in SPS rats than in normal rats, but increased in PRE-084 injection group than in SPS rats. Conclusion The improvement of the activity of neurons in prefrontal cortex of SPS rats by Sigma-1 receptor agonist(PRE-084) might be related to the upregulation of ERK pathway.
关 键 词:创伤后应激障碍 单程长时应激 Sigma-1受体 神经细胞
分 类 号:R749.5[医药卫生—神经病学与精神病学]
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