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罗氏菌素、脑源性神经营养因子与抑制性回避记忆损伤。

Rottlerin, BDNF, and the impairment of inhibitory avoidance memory.

机构信息

Cannabinoid Signaling Laboratory, Department of Psychology, National Cheng Kung University, 1 University Rd, Tainan, 70101, Taiwan.

出版信息

Psychopharmacology (Berl). 2021 Feb;238(2):421-439. doi: 10.1007/s00213-020-05690-x. Epub 2020 Nov 4.

Abstract

RATIONALE AND OBJECTIVE

As a eukaryotic elongation factor 2 kinase (eEF2K) inhibitor and a mitochondrial uncoupler, oncologists have extensively studied rottlerin. Neuroscientists, however, have accumulated scarce data on the role of rottlerin in affective and cognitive functions. Only two prior studies have, respectively, documented its antidepressant-like effect and how it impairs psychostimulant-supported memory. Whether or not rottlerin would affect aversive memory remains unknown. Hence, we sought to investigate the effects of rottlerin on aversive memory in the inhibitory avoidance (IA) task in mice.

MATERIALS AND METHODS

Male C57BL/6J mice were trained to acquire the IA task. Rottlerin (5 mg/kg, i.p. or 3 μg bilaterally in the hippocampus) or the vehicle was administered before footshock training (acquisition), after footshock training (consolidation), after the memory reactivation (reconsolidation), and before the test (retrieval) in the IA task.

RESULTS

Systemic and intrahippocampal rottlerin impaired the acquisition, consolidation, and retrieval of IA memory, without affecting the reconsolidation process. Rottlerin (5 mg/kg, i.p.) induced a fast-onset and long-lasting increase in the brain-derived neurotrophic factor (BDNF) protein levels in the mouse hippocampus. Systemic injection of 7,8-dihydroxyflavone (7,8-DHF, 30 mg/kg), a BDNF tropomyosin receptor kinase B (TrkB) agonist impaired IA memory consolidation, and treatment with K252a (5 μg/kg), a Trk receptor antagonist, reversed the suppressing effect of rottlerin on IA memory consolidation.

CONCLUSION

Rottlerin impairs IA memory consolidation through the enhancement of BDNF signaling in the mouse hippocampus. Excessive brain BDNF levels can be detrimental to cognitive function. Rottlerin is likely to affect the original memory-associated neuroplasticity. Thus, it can be combined with exposure therapy to facilitate the forgetting of maladaptive aversive memory, such as post-traumatic stress disorder (PTSD).

摘要

背景与目的

作为一种真核延伸因子 2 激酶(eEF2K)抑制剂和线粒体解偶联剂,肿瘤学家已经广泛研究了罗特林。然而,神经科学家对罗特林在情感和认知功能中的作用积累的资料甚少。仅有两项先前的研究分别记录了其抗抑郁样作用以及它如何损害精神兴奋剂支持的记忆。罗特林是否会影响厌恶记忆仍不清楚。因此,我们试图研究罗特林对小鼠抑制性回避(IA)任务中厌恶记忆的影响。

材料与方法

雄性 C57BL/6J 小鼠接受训练以获得 IA 任务。罗特林(5mg/kg,腹腔内注射或双侧海马内 3μg)或载体在足部电击训练前(获得)、足部电击训练后(巩固)、记忆再激活后(再巩固)和 IA 任务测试前(检索)给予。

结果

系统和海马内罗特林损害了 IA 记忆的获得、巩固和检索,而不影响再巩固过程。罗特林(5mg/kg,腹腔内注射)诱导了快速起始和长期持续增加小鼠海马脑源性神经营养因子(BDNF)蛋白水平。系统注射 7,8-二羟基黄酮(7,8-DHF,30mg/kg),一种 BDNF 原肌球蛋白受体激酶 B(TrkB)激动剂,损害了 IA 记忆的巩固,而用 Trk 受体拮抗剂 K252a(5μg/kg)处理可逆转罗特林对 IA 记忆巩固的抑制作用。

结论

罗特林通过增强小鼠海马内的 BDNF 信号来损害 IA 记忆的巩固。大脑中过多的 BDNF 水平可能对认知功能有害。罗特林可能会影响原始记忆相关的神经可塑性。因此,它可以与暴露疗法结合使用,以促进对适应不良的厌恶记忆(如创伤后应激障碍)的遗忘。

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