Serafim K R, Russo P S T, Fernandes C E M, Gianlorenço A C L, Mattioli R
Laboratório de Neurociências, Departamento de Fisioterapia, Centro de Ciências Biológicas e da Sáude, Universidade Federal de São Carlos, Rod. Washington Luis, Km 235, 13565-905 Sao Carlos, Brazil.
Laboratório de Biologia de Sistemas Computacional-Departamento de Análises Clínicas, Departamento de Ciências Farmacêuticas, Universidade de São Paulo, Av. Prof. Lineu Prestes, 580 Butantã, Brazil.
Brain Res Bull. 2016 Jul;125:127-33. doi: 10.1016/j.brainresbull.2016.06.006. Epub 2016 Jun 23.
H1 receptor histaminergic antagonist, chlorpheniramine (CPA) participates in cognitive performance in various animal models. However, little is known regarding the effects of CPA microinjection into the amygdala on emotional behavior. The purpose of this study was to investigate whether CPA microinjection into the amygdala has the same effect on two models, one anxiety- and the other fear-mediated, in various memory stages using the elevated plus maze (EPM) and the inhibitory avoidance task (IAT) tests. Two experiments were performed with seventy-two adult male Swiss mice. Behavioral testing was performed on two consecutive days, and in both experiments, before each trial, the animals received bilateral microinjections of saline (SAL) or CPA (0.16 nmol). The animals were re-exposed to the EPM or IAT 24h after the first trial. Four experimental groups were tested: SAL-SAL, SAL-CPA, CPA-SAL and CPA-CPA. In experiment 1, a decreased open arm exploration (% open arm entries, %OAE and% open arms time, %OAT) for SAL-SAL and SAL-CPA was showed, while these measures did not decrease for the CPA-SAL and CPA-CPA groups in Trial 2. In experiment 2, an increase of retention latency in relation to training 2 for the groups SAL-SAL and CPA-SAL and a significant decrease in latency for the group SAL-CPA was revealed. These results indicate that chlorpheniramine microinjection into the amygdala impairs emotional memory acquisition and/or consolidation in the EPM and retrieval of IAT.
H1 受体组胺能拮抗剂氯苯那敏(CPA)在多种动物模型中参与认知表现。然而,关于向杏仁核微量注射 CPA 对情绪行为的影响却知之甚少。本研究的目的是使用高架十字迷宫(EPM)和抑制性回避任务(IAT)测试,调查向杏仁核微量注射 CPA 在不同记忆阶段对两种模型(一种由焦虑介导,另一种由恐惧介导)是否具有相同的作用。对 72 只成年雄性瑞士小鼠进行了两项实验。连续两天进行行为测试,在两个实验中,每次试验前,动物均接受双侧微量注射生理盐水(SAL)或 CPA(0.16 nmol)。在第一次试验后 24 小时,让动物再次接触 EPM 或 IAT。测试了四个实验组:SAL-SAL、SAL-CPA、CPA-SAL 和 CPA-CPA。在实验 1 中,SAL-SAL 和 SAL-CPA 组的开放臂探索减少(开放臂进入百分比,%OAE 和开放臂时间百分比,%OAT),而在试验 2 中,CPA-SAL 和 CPA-CPA 组的这些指标并未降低。在实验 2 中,SAL-SAL 和 CPA-SAL 组相对于训练 2 的记忆保持潜伏期增加,而 SAL-CPA 组的潜伏期显著缩短。这些结果表明,向杏仁核微量注射氯苯那敏会损害 EPM 中的情绪记忆获取和/或巩固以及 IAT 的记忆提取。