王任烨, 俞雪锋, 谢昫珮, 潘建春. 氟西汀对恐惧记忆形成阶段BDNF、Bcl-2表达的影响J. 药学学报, 2014,49(4): 463-469.
引用本文: 王任烨, 俞雪锋, 谢昫珮, 潘建春. 氟西汀对恐惧记忆形成阶段BDNF、Bcl-2表达的影响J. 药学学报, 2014,49(4): 463-469.
WANG Ren-ye, YU Xue-feng, XIE Xu-pei, PAN Jian-chun. Effect of fluoxetine on the expressions of BDNF and Bcl-2 during fear memory formationJ. Acta Pharmaceutica Sinica, 2014,49(4): 463-469.
Citation: WANG Ren-ye, YU Xue-feng, XIE Xu-pei, PAN Jian-chun. Effect of fluoxetine on the expressions of BDNF and Bcl-2 during fear memory formationJ. Acta Pharmaceutica Sinica, 2014,49(4): 463-469.

氟西汀对恐惧记忆形成阶段BDNF、Bcl-2表达的影响

Effect of fluoxetine on the expressions of BDNF and Bcl-2 during fear memory formation

  • 摘要: 研究氟西汀对小鼠恐惧记忆形成过程中海马、前额叶皮质及杏仁核BDNF和Bcl-2表达的影响。取48只雄性ICR小鼠,随机分为空白对照组、条件性恐惧刺激组(conditioned fear group,CF)和氟西汀+条件性 恐惧刺激组(FLX+CF group)。电击刺激后1 h和24 h分别观察僵立时间;Western blotting检测海马、前额叶皮质及杏仁核BDNF、Bcl-2的表达。结果显示,24 h后,FLX+CF组僵立时间百分比为(19.4 ± 2.2)%,显著低于CF组(29.9 ± 4.2)%;电击刺激1天后,FLX+CF组海马Bcl-2蛋白表达显著增加(P <0.001),BDNF表达无明显差异;7天后,Bcl-2蛋白表达无明显差异,BDNF表达显著增加(P <0.001);额叶及杏仁核BDNF和Bcl-2表达与CF组相比无明显差异。结果表明,氟西汀通过上调海马Bcl-2及BDNF的表达,发挥中枢神经保护作用,从而影响恐惧记忆的形成。

     

    Abstract: The aim of this study is to investigate the effect of fluoxetine (FLX) on the expressions of BDNF and Bcl-2 in the hippocampus, the amygdala and the prefrontal cortex of conditioned fear (CF) model mice. Forty eight mice were randomly divided into three groups, normal control group, CF stress group and FLX-pretreated CF group. The FLX-pretreated CF group was given FLX (10 mg·kg-1·d-1) for 7 days before CF stress. After CF stress model was established, all mice were given behavioral experiments to test whether FLX impaired or improved the auditory and contextual fear conditioning. Then mice were sacrificed. The expressions of BDNF and Bcl-2 were detected by Western blotting. The results showed that the freezing time of FLX-pretreated CF group was significantly lower than that of CF group; FLX pretreatment up-regulated the expression of Bcl-2 in the hippocampus at 1 d after CF stress (P < 0.001), but no significant differences was observed at 7 d; BDNF significantly increased in the hippocampus at 7 d (P < 0.001), but no differences at 1 d; the expressions of BDNF and Bcl-2 in the amygdala and the prefrontal cortex were of no obvious differences between CF group and FLX-pretreated CF group at 1 d or 7 d after CF stress. Parallel to these changes, pretreatment with FLX could affect histopathologic changes induced by CF stress. Furthermore, the results indicated that FLX pretreatment could protect against CF stress-induced neurological damage via the activation of BDNF and Bcl-2 in hippocampus.

     

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