Instituto de Biología Celular y Neurociencias "Prof. Eduardo de Robertis", Facultad de Medicina, Universidad de Buenos Aires-CONICET, Paraguay 2155, 3rd Floor, C1121ABG, Buenos Aires, Argentina.
Instituto Tecnológico de Buenos Aires, Buenos Aires, Argentina.
Sci Rep. 2023 Aug 19;13(1):13507. doi: 10.1038/s41598-023-40434-9.
The fate of memories depends mainly on two opposing forces: the mechanisms required for the storage and maintenance of memory and the mechanisms underlying forgetting, being the latter much less understood. Here, we show the effect of inhibiting the small Rho GTPase Rac1 on the fate of inhibitory avoidance memory in male rats. The immediate post-training micro-infusion of the specific Rac1 inhibitor NSC23766 (150 ng/0.5 µl/ side) into the ventral tegmental area (VTA) enhanced long-term memory at 1, 7, and 14 days after a single training. Additionally, an opposed effect occurred when the inhibitor was infused at 12 h after training while no effect was observed immediately after testing animals at 1 day. Control experiments ruled out the possibility that post-training memory enhancement was due to facilitation of memory formation since no effect was found when animals were tested at 1 h after acquisition and no memory enhancement was observed after the formation of a weak memory. Immediate post-training micro-infusion of Rac1 inhibitor into the dorsal hippocampus, or the amygdala did not affect memory. Our findings support the idea of a Rac1-dependent time-specific active forgetting mechanism in the VTA controlling the strength of a long-term aversive memory.
存储和维持记忆的机制,以及遗忘的基础机制,后者的理解要少得多。在这里,我们展示了抑制小 Rho GTPase Rac1 对雄性大鼠抑制性回避记忆命运的影响。在单次训练后,立即将特异性 Rac1 抑制剂 NSC23766(150ng/0.5µl/侧)微量注入腹侧被盖区(VTA),可增强 1、7 和 14 天后的长期记忆。此外,当抑制剂在训练后 12 小时注入时,会产生相反的效果,而在 1 天后立即测试动物时则没有效果。对照实验排除了训练后记忆增强是由于记忆形成促进的可能性,因为当动物在获得后 1 小时测试时,没有发现效果,并且在形成弱记忆后,也没有观察到记忆增强。立即在训练后将 Rac1 抑制剂微量注入背侧海马体或杏仁核,不会影响记忆。我们的发现支持了 Rac1 依赖性的、时间特异性的主动遗忘机制在 VTA 中控制长期厌恶记忆强度的观点。