首页> 外文期刊>Behavioural Brain Research: An International Journal >Nicotine enhances trace cued fear conditioning but not delay cued fear conditioning in C57BL/6 mice.
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Nicotine enhances trace cued fear conditioning but not delay cued fear conditioning in C57BL/6 mice.

机译:尼古丁增强了C57BL / 6小鼠的线索暗示恐惧条件,但并未延迟线索暗示恐惧条件。

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摘要

Nicotine facilitates hippocampus-dependent contextual but not hippocampus-independent cued delay fear conditioning. To test if the effects of nicotine are specific to contextual fear conditioning or would extend to another hippocampus-dependent version of fear conditioning, we compared the effects of nicotine on cued delay and cued trace fear conditioning in male and female C57BL/6 mice. Unlike cued delay fear conditioning, cued trace fear conditioning is hippocampus dependent. Thus, if nicotine enhances hippocampus-dependent fear conditioning, nicotine should enhance trace fear conditioning. For both trace and delay conditioning, five 30s, 85dB white noise conditioned stimuli (CS) were paired with five 2s, 0.5mA footshock unconditioned stimuli (US). In the trace paradigm, a 30-s period was inserted between CS offset and US onset. The CS and US co-terminated in the delay paradigm. Testing occurred 24h later. The data indicate that nicotine (given on training and testing day) enhances trace but not delay cued fear conditioning. No sex differences were found. For delay cued fear conditioning a high level of freezing to the CS was found. Thus, a second experiment examined if the lack of enhancement of delay cued fear conditioning by nicotine was due to a ceiling effect. The CS duration was decreased to 15s and only one CS-US pairing was used for delay and trace cued fear conditioning. Although overall levels of freezing to the cue were lower in the second experiment, nicotine still enhanced trace fear conditioning but did not enhance delay fear conditioning. Taken together, the results of the present experiments suggest that nicotine enhances hippocampus-dependent versions of fear conditioning.
机译:尼古丁促进海马依赖性背景,但不促进海马非依赖性提示延迟恐惧条件。为了测试尼古丁的作用是否特定于情境恐惧条件,或是否会扩展到另一种海马依赖型恐惧条件,我们比较了尼古丁对雄性和雌性C57BL / 6小鼠提示延迟和提示痕量恐惧条件的影响。与提示延迟恐惧条件不同,提示微量恐惧条件是海马依赖的。因此,如果尼古丁增强了海马依赖性恐惧条件,则尼古丁应增强痕量恐惧条件。对于跟踪和延迟调理,将五个30s,85dB白噪声条件刺激(CS)与五个2s,0.5mA脚震非条件刺激(US)配对。在跟踪范例中,在CS偏移量和US发作之间插入了30秒的周期。 CS和美国在延迟范式上共同终结。测试在24小时后进行。数据表明(在训练和测试日给予)尼古丁可增强痕量,但不会延迟暗示的恐惧条件。未发现性别差异。出于延迟提示恐惧的条件,发现对CS的冻结程度很高。因此,第二个实验检查了尼古丁缺乏延迟提示恐惧条件的增强是否归因于上限效应。 CS持续时间减少到15s,仅使用一个CS-US配对进行延迟和线索提示的恐惧调节。尽管在第二个实验中冻结到提示的总体水平较低,但尼古丁仍然增强了痕量恐惧条件,但没有增强延迟恐惧条件。两者合计,本实验的结果表明,尼古丁增强了海马依赖型恐惧条件。

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