首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >PNAS Plus: Memory retrieval of inhibitory avoidance requires histamine H1 receptor activation in the hippocampus
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PNAS Plus: Memory retrieval of inhibitory avoidance requires histamine H1 receptor activation in the hippocampus

机译:PNAS Plus:抑制性记忆的记忆恢复需要海马中的组胺H1受体激活

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摘要

Retrieval represents a dynamic process that may require neuromodulatory signaling. Here, we report that the integrity of the brain histaminergic system is necessary for retrieval of inhibitory avoidance (IA) memory, because rats depleted of histamine through lateral ventricle injections of α-fluoromethylhistidine (a-FMHis), a suicide inhibitor of histidine decarboxylase, displayed impaired IA memory when tested 2 d after training. a-FMHis was administered 24 h after training, when IA memory trace was already formed. Infusion of histamine in hippocampal CA1 of brain histamine-depleted rats (hence, amnesic) 10 min before the retention test restored IA memory but was ineffective when given in the basolateral amygdala (BLA) or the ventral medial prefrontal cortex (vmPFC). Intra-CA1 injections of selective H1 and H2 receptor agonists showed that histamine exerted its effect by activating the H1 receptor. Noteworthy, the H1 receptor antagonist pyrilamine disrupted IA memory retrieval in rats, thus strongly supporting an active involvement of endogenous histamine; 90 min after the retention test, c-Fos–positive neurons were significantly fewer in the CA1s of a-FMHis–treated rats that displayed amnesia compared with in the control group. We also found reduced levels of phosphorylated cAMP-responsive element binding protein (pCREB) in the CA1s of a-FMHis–treated animals compared with in controls. Increases in pCREB levels are associated with retrieval of associated memories. Targeting the histaminergic system may modify the retrieval of emotional memory; hence, histaminergic ligands might reduce dysfunctional aversive memories and improve the efficacy of exposure psychotherapies.
机译:检索代表可能需要神经调节信号的动态过程。在这里,我们报告说,大脑组胺能系统的完整性对于恢复抑制性逃避(IA)记忆是必要的,因为大鼠通过侧脑室注射组氨酸脱羧酶的自杀抑制剂α-氟甲基组氨酸(a-FMHis)消耗了组胺,训练后2天测试时显示IA记忆受损。训练后24小时给予a-FMHis,此时已形成IA记忆痕迹。保留测试前10分钟,在脑组胺耗尽的大鼠海马CA1中注入组胺(因此,记忆删除)恢复了IA记忆,但在基底外侧杏仁核(BLA)或腹内侧前额叶皮层(vmPFC)中给药无效。选择性H1和H2受体激动剂的CA1内注射显示组胺通过激活H1受体发挥其作用。值得注意的是,H1受体拮抗剂吡拉明破坏了大鼠的IA记忆恢复,因此强烈支持了内源性组胺的积极参与。保留测试后90分钟,与遗忘症组相比,经a-FMHis治疗的表现出健忘症的大鼠CA1中c-Fos阳性神经元明显减少。我们还发现,与对照组相比,经a-FMHis处理的动物的CA1中磷酸化的cAMP反应元件结合蛋白(pCREB)含量降低。 pCREB水平的增加与相关记忆的检索有关。针对组织胺能系统可能会改变情绪记忆的恢复;因此,组胺能配体可能减少功能障碍性厌恶记忆并提高暴露心理治疗的功效。

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