Autophagy Enhances Memory Erasure through Synaptic Destabilization

作者：Shehata Mohammad^*; Abdou Kareem; Choko Kiriko; Matsuo Mina; Nishizono Hirofumi; Inokuchi Kaoru^*

来源：Journal of Neuroscience, 2018, 38(15): 3809-3822.

DOI：10.1523/JNEUROSCI.3505-17.2018

• AMPA receptors
• long-term potentiation
• NMDA receptors
• post-traumatic stress disorder
• protein degradation
• reconsolidation

There is substantial interest in memory reconsolidation as a target for the treatment of anxiety disorders, such as post-traumatic stress disorder. However, its applicability is restricted by reconsolidation-resistant boundary conditions that constrain the initial memory destabilization. In this study, we investigated whether the induction of synaptic protein degradation through autophagy modulation, a major protein degradation pathway, can enhance memory destabilization upon retrieval and whether it can be used to overcome these conditions. Here, using male mice in an auditory fear reconsolidation model, we showed that autophagy contributes to memory destabilization and its induction can be used to enhance erasure of a reconsolidation-resistant auditory fear memory that depended on AMPAR endocytosis. Using male mice in a contextual fear reconsolidation model, autophagy induction in the amygdala or in the hippocampus enhanced fear or contextual memory destabilization, respectively. The latter correlated with AMPAR degradation in the spines of the contextual memory-ensemble cells. Using male rats in an in vivo LTP reconsolidation model, autophagy induction enhanced synaptic destabilization in an NMDAR-dependent manner. These data indicate that induction of synaptic protein degradation can enhance both synaptic and memory destabilization upon reactivation and that autophagy inducers have the potential to be used as a therapeutic tool in the treatment of anxiety disorders.

• 出版日期2018-4-11