4.3 Article

Two waves of proteasome-dependent protein degradation in the hippocampus are required for recognition memory consolidation

Journal

NEUROBIOLOGY OF LEARNING AND MEMORY
Volume 120, Issue -, Pages 1-6

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.nlm.2015.02.005

Keywords

Proteasome; Lactacystin; Protein degradation; Hippocampus; Object recognition; Recognition memory

Funding

  1. National Council for Scientific and Technological Development (CNPq) [308144/2012-0, 484185/2012-8, 303276/2013-4]
  2. PNPD CAPES/HCPA [0130110]
  3. National Institute for Translational Medicine (INCT-TM)
  4. HCPA institutional research fund (FIPE/HCPA)
  5. PROBIC/FAPERGS fellowship
  6. PIBIC/CNPq fellowship

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Healthy neuronal function and synaptic modification require a concert of synthesis and degradation of proteins. Increasing evidence indicates that protein turnover mediated by proteasome activity is involved in long-term synaptic plasticity and memory. However, its role in different phases of memory remains debated, and previous studies have not examined the possible requirement of protein degradation in recognition memory. Here, we show that the proteasome inhibitor, lactacystin (LAC), infused into the CA1 area of the hippocampus at two specific time points during consolidation, impairs 24-retention of memory for object recognition in rats. Administration of LAC after retrieval did not affect retention. These findings provide the first evidence for a requirement of proteasome activity in recognition memory, indicate that protein degradation in the hippocampus is necessary during selective time windows of memory consolidation, and further our understanding of the role of protein turnover in memory formation. (C) 2015 Elsevier Inc. All rights reserved.

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