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抗组胺药损害恐惧记忆的巩固和表达。

Impairment of fear memory consolidation and expression by antihistamines.

机构信息

Laboratory of Chemical Pharmacology, Graduate School of Pharmaceutical Sciences, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-0033, Japan.

出版信息

Brain Res. 2013 Feb 1;1493:19-26. doi: 10.1016/j.brainres.2012.11.030. Epub 2012 Nov 23.

Abstract

Antihistamines are widely used to treat allergy symptoms. First-generation antihistamines have adverse effects on the central nervous system (CNS), such as hypnotic and amnesic effects, whereas second-generation antihistamines have poor brain penetration, and therefore, have fewer CNS-related adverse effects. Memory consists of several phases, including acquisition, consolidation, expression, and extinction. It remains unclear whether these phases are affected by antihistamines. We investigated the effects of diphenhydramine, a first-generation antihistamine, and levocetirizine and olopatadine, second-generation antihistamines, on memory phases. Mice were subjected to fear conditioning on day 1 and tested on day 2. Antihistamines were administered before conditioning, immediately after conditioning, or before the test session. Diphenhydramine (30mg/kg) decreased freezing time when administered immediately after conditioning or before the test session. These effects were not attributable to a change in locomotor activity. Levocetirizine (0.1, 1, 10mg/kg) and olopatadine (1, 10, 20mg/kg) had no effects on conditioned fear. We also examined the effect of diphenhydramine and levocetirizine on the expression of an activity-dependent gene associated with the test session. Diphenhydramine, but not levocetirizine, increased Arc transcription in the central nucleus of the amygdala. These data indicate that diphenhydramine, but not levocetirizine or olopatadine, impairs the consolidation and expression of conditioned fear.

摘要

抗组胺药被广泛用于治疗过敏症状。第一代抗组胺药对中枢神经系统(CNS)有不良影响,如催眠和健忘作用,而第二代抗组胺药脑穿透性差,因此 CNS 相关不良反应较少。记忆包括几个阶段,包括获取、巩固、表达和遗忘。目前尚不清楚这些阶段是否受到抗组胺药的影响。我们研究了第一代抗组胺药苯海拉明和第二代抗组胺药左西替利嗪和奥洛他定对记忆阶段的影响。小鼠在第 1 天进行恐惧条件反射,在第 2 天进行测试。抗组胺药在条件反射前、条件反射后立即或测试前给药。苯海拉明(30mg/kg)在条件反射后立即或测试前给药时,可减少冻结时间。这些影响与运动活性的变化无关。左西替利嗪(0.1、1、10mg/kg)和奥洛他定(1、10、20mg/kg)对条件性恐惧无影响。我们还研究了苯海拉明和左西替利嗪对与测试阶段相关的活性依赖性基因表达的影响。苯海拉明而非左西替利嗪增加了杏仁中央核中 Arc 转录。这些数据表明,苯海拉明而非左西替利嗪或奥洛他定损害了条件性恐惧的巩固和表达。

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