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首页> 外文期刊>Behavioural Brain Research: An International Journal >Histamine H3 antagonist thioperamide dose-dependently enhances memory consolidation and reverses amnesia induced by dizocilpine or scopolamine in a one-trial inhibitory avoidance task in mice.
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Histamine H3 antagonist thioperamide dose-dependently enhances memory consolidation and reverses amnesia induced by dizocilpine or scopolamine in a one-trial inhibitory avoidance task in mice.

机译:组胺H3拮抗剂硫代过酰胺剂量依赖性地增强记忆巩固并逆转由地佐西平或东pol碱引起的健忘症,这在小鼠的一次试验性抑制回避任务中。

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摘要

In the literature, there is some evidence indicating that H3 histamine receptor antagonists, in particular thioperamide, can facilitate learning and memory retrieval in laboratory rodents. The present study aimed at verifying whether this also holds for memory consolidation, a phase of memory for which there is scarcity of convincing data on the effects of H3 receptor antagonists given systemically. To that end, memory consolidation was assessed in C57BL/6J mice using the one-trial step-through inhibitory avoidance task, the compounds being injected immediately after training (foot-shock) and performance measured 24h later. More specifically, the following effects of thioperamide (1.25-20mg/kg) were dose-dependently analysed: (1) its potential direct effects on memory consolidation; (2) its potential reversing effects on retrograde amnesia induced by the NMDA antagonist dizocilpine (MK-801, 0.5mg/kg) and (3) its potential reversing effects on the well-known amnesia induced by the muscarinic antagonist scopolamine (0.25mg/kg). We found that thioperamide exerted a dose-dependent facilitative effect on memory consolidation. Furthermore, the H3 receptor antagonist reversed scopolamine- and especially dizocilpine-induced amnesia. The results strongly support the view that the brain mechanisms of memory consolidation involve a functional interaction between the NMDA and the H3 sites.
机译:在文献中,有一些证据表明,H3组胺受体拮抗剂,特别是硫代过酰胺,可以促进实验室啮齿动物的学习和记忆恢复。本研究旨在验证这是否也适用于记忆巩固,这是记忆的一个阶段,缺乏关于全身给予的H3受体拮抗剂作用的令人信服的数据。为此,在C57BL / 6J小鼠中使用一次尝试性逐步抑制性避免任务评估了记忆巩固,在训练后立即注射化合物(足部电击),并在24小时后测量性能。更具体地说,对硫代过酰胺(1.25-20mg / kg)的以下作用进行了剂量依赖性分析:(1)其对记忆巩固的潜在直接作用; (2)NMDA拮抗剂地佐西平(MK-801,0.5mg / kg)对逆行性健忘的潜在逆转作用;(3)毒蕈碱拮抗剂东pol碱(0.25mg / kg)对众所周知的健忘的逆转作用公斤)。我们发现硫代过酰胺对记忆巩固发挥剂量依赖性的促进作用。此外,H3受体拮抗剂逆转了东pol碱,特别是地佐西平诱导的健忘症。结果强烈支持以下观点,即记忆巩固的大脑机制涉及NMDA和H3位点之间的功能相互作用。

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