The Role of Prelimbic and Anterior Cingulate Cortices in Fear Memory Reconsolidation and Persistence Depends on the Memory Age

• Published in: Learning & memory (Cold Spring Harbor, N.Y.) Vol. 27; no. 8; pp. 292 - 300
• Main Authors: da Silva, Thiago Rodrigues, Sohn, Jeferson Machado Batista, Andreatini, Roberto, Stern, Cristina Aparecida
• Format: Journal Article
• Language: English
• Published: United States Cold Spring Harbor Laboratory Press 01-08-2020
• Subjects: Age; Animals; Behavior, Animal - drug effects; Behavior, Animal - physiology; Brain; Brain Hemisphere Functions; Conditioning; Fear; Fear - physiology; Fear conditioning; Gyrus Cinguli - drug effects; Gyrus Cinguli - physiology; Kinases; Male; Memory; Memory Consolidation - drug effects; Memory Consolidation - physiology; Memory, Long-Term - drug effects; Memory, Long-Term - physiology; Memory, Short-Term - drug effects; Memory, Short-Term - physiology; Mental Recall - drug effects; Mental Recall - physiology; Persistence; Protein kinase C; Rats; Rats, Wistar; Recall (Psychology); Rodents; Selective Estrogen Receptor Modulators - pharmacology; Tamoxifen; Tamoxifen - pharmacology; Time Factors
• ISSN: 1072-0502; 1549-5485; 1549-5485
• DOI: 10.1101/lm.051615.120

Reconsolidation is a time-limited process under which reactivated memory content can be modified. Works focused on studying reconsolidation mainly restrict intervention to the moments immediately after reactivation and to recently acquired memories. However, the brain areas activated during memory retrieval depend on when it was acquired, and it is relatively unknown how different brain sites contribute to reconsolidation and persistence of reactivated recent and remote fear memories. Here, we sought to investigate the participation of prelimbic (PL) and anterior cingulate cortices (ACC) in recent (1 d old) and remote (21 d old) fear memory reconsolidation and persistence. Male Wistar rats were submitted to the contextual fear conditioning protocol. Tamoxifen (TMX), an estrogen receptor modulator known to inhibit protein kinase C activity was used to interfere with these processes. When infused into the PL cortex, but not into the ACC, TMX administration immediately or 6 h after recent fear memory reactivation impaired memory reconsolidation and persistence, respectively. TMX administered immediately after remote memory reactivation impaired memory reconsolidation when infused into the PL cortex and ACC. However, remote memory persistence was only affected when TMX was infused 6 h after memory reactivation into the ACC and no effect was observed when TMX was infused 6 h after memory reactivation into PL cortex. Together, the findings provide further evidence on the participation of PL cortex and ACC in reconsolidation of recent and remote fear memories and suggest that the persistence of a reactivated fear memory becomes independent on the PL cortex with memory age and dependent on the ACC.