Systemic corticosterone administration impairs the late fear memory reconsolidation via basolateral amygdala glucocorticoid receptors: Dependence on the time window and memory age

IF 2.2 4区 心理学 Q3 BEHAVIORAL SCIENCES
Maryam Nazari , Ali Rashidy-Pour , Abbas Ali Vafaei , Payman Raise-Abdullahi
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引用次数: 1

Abstract

Glucocorticoid receptors (GRs) of the basolateral amygdala (BLA) play an important role in memory reconsolidation. The present study investigated the role of the BLA GRs in the late reconsolidation of fear memory using an inhibitory avoidance (IA) task in male Wistar rats. Stainless steel cannulae were implanted bilaterally into the BLA of the rats. After 7 days of recovery, the animals were trained in a one-trial IA task (1 mA, 3 s). In Experiment One, 48 h after the training session, the animals received 3 systemic doses of corticosterone (CORT; 1, 3, or 10 mg/kg, i.p.) followed by an intra-BLA microinjection of the vehicle (0.3 µl/side) at different time points (immediately, 12, or 24 h) after memory reactivation. Memory reactivation was performed by returning the animals to the light compartment while the sliding door was open. No shock was delivered during memory reactivation. CORT (10 mg/kg) injection 12 h after memory reactivation most effectively impaired the late memory reconsolidation (LMR). In the second part of Experiment One, immediately, 12, or 24 h after memory reactivation, GR antagonist RU38486 (RU; 1 ng/0.3 µl/side) was injected into BLA following a systemic injection of CORT (10 mg/kg) to examine whether it would block the CORT effect. RU inhibited the impairing effects of CORT on LMR. In Experiment Two, the animals received CORT (10 mg/kg) with time windows immediately, 3, 6, 12, and 24 h after memory reactivation. Again, CORT (10 mg/kg) injection 12 h after memory reactivation impaired LMR. Memory reactivation was performed in the third Experiment, 7, 14, 28, or 56 days after the training session. Injection of CORT (10 mg/kg) 12 h later had no significant effect on the LMR. The impairing effect of CORT was seen only in 2-day-old but not 7, 14, 28, and 56-day-old memories. GRs located in BLA seem to play an important role in the LMR of young memory, as with increasing the age of memories, they become less sensitive to manipulation.

皮质酮对基底外侧杏仁核糖皮质激素受体晚期恐惧记忆再巩固的影响:对时间窗和记忆年龄的依赖
基底外侧杏仁核(BLA)糖皮质激素受体(GRs)在记忆再巩固中起重要作用。本研究在雄性Wistar大鼠的抑制性回避(IA)任务中研究了BLA GRs在恐惧记忆后期再巩固中的作用。双侧在大鼠BLA内植入不锈钢管。恢复7天后,动物接受单次IA任务(1 mA, 3 s)的训练。在实验一中,训练后48 h,动物接受3次全身剂量的皮质酮(CORT;1、3或10 mg/kg, i.p),然后在记忆重新激活后的不同时间点(立即、12或24小时)将载物(0.3 μ l/侧)注射到bla内。在滑动门打开的情况下,通过让动物回到有光的隔间来重新激活记忆。在记忆重新激活过程中没有电击。记忆再激活后12 h注射CORT (10 mg/kg)对后期记忆再巩固(LMR)的损害最为显著。在实验一的第二部分,记忆再激活后立即、12或24小时,GR拮抗剂RU38486 (RU;在全身注射CORT (10 mg/kg)后,在BLA中注射1 ng/0.3µl/侧),观察其是否会阻断CORT的作用。RU抑制CORT对LMR的损害作用。在实验二中,动物在记忆再激活后立即、3、6、12和24 h给予CORT (10 mg/kg)。同样,在记忆再激活后12小时注射CORT (10 mg/kg)会损害LMR。在第三个实验中,分别在训练结束后的第7天、第14天、第28天和第56天进行记忆再激活。12 h后注射CORT (10 mg/kg)对LMR无显著影响。CORT的损害作用仅在第2天记忆中发现,而在第7、14、28和56天记忆中没有发现。位于BLA的GRs似乎在年轻记忆的LMR中起着重要作用,因为随着记忆年龄的增加,它们对操纵变得不那么敏感。
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来源期刊
CiteScore
5.10
自引率
7.40%
发文量
77
审稿时长
12.6 weeks
期刊介绍: Neurobiology of Learning and Memory publishes articles examining the neurobiological mechanisms underlying learning and memory at all levels of analysis ranging from molecular biology to synaptic and neural plasticity and behavior. We are especially interested in manuscripts that examine the neural circuits and molecular mechanisms underlying learning, memory and plasticity in both experimental animals and human subjects.
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