Rothwell Cailin M, Lukowiak Ken D
Hotchkiss Brain Institute, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada.
Commun Integr Biol. 2017 Apr 3;10(3):e1306616. doi: 10.1080/19420889.2017.1306616. eCollection 2017.
Stressor-induced memory enhancement has previously been shown to involve DNA methylation in the mollusc . Specifically, injection of the DNA methylation inhibitor 5-AZA one hour before exposure to a memory-enhancing stressor obstructs memory augmentation. However, the duration of the influence of 5-AZA on this memory enhancement has not yet been examined. In this study, 2 memory-enhancing stressors (a thermal stress and exposure to the scent of a predator) were used to examine whether injection of the DNA methylation inhibitor 5-AZA 24 hours before stress exposure would still impair memory enhancement. Indeed, it was observed that memory is still obstructed when 5-AZA is injected 24 hours before exposure to either of these stressors in . Understanding that 5-AZA still effectively impairs memory enhancement after a period of 24 hours is valuable because it indicates that experimental manipulations do not need to be made within one hour after the injection of this DNA methylation inhibitor and can instead be made within one day (i.e. 24 hours). These results will allow for a future examination of the possible involvement of DNA methylation in memory enhancement related to longer-term stressors or environmental changes. This study further elucidates the involvement of epigenetic changes in memory enhancement in , providing insight into the process of memory formation in this mollusc.
应激源诱导的记忆增强先前已被证明涉及软体动物的DNA甲基化。具体而言,在暴露于增强记忆的应激源前一小时注射DNA甲基化抑制剂5-氮杂胞苷会阻碍记忆增强。然而,5-氮杂胞苷对这种记忆增强的影响持续时间尚未得到研究。在本研究中,使用了两种增强记忆的应激源(热应激和暴露于捕食者的气味)来检验在应激暴露前24小时注射DNA甲基化抑制剂5-氮杂胞苷是否仍会损害记忆增强。事实上,观察到在暴露于这些应激源中的任何一种之前24小时注射5-氮杂胞苷时,记忆仍然受到阻碍。了解到5-氮杂胞苷在24小时后仍能有效损害记忆增强是有价值的,因为这表明实验操作不需要在注射这种DNA甲基化抑制剂后一小时内进行,而是可以在一天内(即24小时)进行。这些结果将有助于未来研究DNA甲基化在与长期应激源或环境变化相关的记忆增强中可能的作用。本研究进一步阐明了表观遗传变化在该软体动物记忆增强中的作用,为该软体动物的记忆形成过程提供了见解。