Specific requirement of NMDA receptors for long-term memory consolidation in Drosophila ellipsoid body

Nat Neurosci. 2007 Dec;10(12):1578-86. doi: 10.1038/nn2005. Epub 2007 Nov 4.

Abstract

In humans and many other animals, memory consolidation occurs through multiple temporal phases and usually involves more than one neuroanatomical brain system. Genetic dissection of Pavlovian olfactory learning in Drosophila melanogaster has revealed multiple memory phases, but the predominant view holds that all memory phases occur in mushroom body neurons. Here, we demonstrate an acute requirement for NMDA receptors (NMDARs) outside of the mushroom body during long-term memory (LTM) consolidation. Targeted dsRNA-mediated silencing of Nmdar1 and Nmdar2 (also known as dNR1 or dNR2, respectively) in cholinergic R4m-subtype large-field neurons of the ellipsoid body specifically disrupted LTM consolidation, but not retrieval. Similar silencing of functional NMDARs in the mushroom body disrupted an earlier memory phase, leaving LTM intact. Our results clearly establish an anatomical site outside of the mushroom body involved with LTM consolidation, thus revealing both a distributed brain system subserving olfactory memory formation and the existence of a system-level memory consolidation in Drosophila.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Analysis of Variance
  • Animals
  • Animals, Genetically Modified
  • Association Learning / drug effects
  • Association Learning / physiology*
  • Behavior, Animal
  • Brain / cytology*
  • Conditioning, Classical
  • Drosophila
  • Drosophila Proteins / genetics
  • Maze Learning
  • Memory / drug effects
  • Memory / physiology*
  • Mushroom Bodies / drug effects
  • Mushroom Bodies / physiology
  • Neurons / physiology*
  • Odorants
  • RNA, Double-Stranded / pharmacology
  • Receptors, N-Methyl-D-Aspartate / genetics
  • Receptors, N-Methyl-D-Aspartate / physiology*
  • Time Factors

Substances

  • Drosophila Proteins
  • NR1 NMDA receptor
  • NR2A NMDA receptor
  • RNA, Double-Stranded
  • Receptors, N-Methyl-D-Aspartate