Antisense hippocampal knockdown of NMDA-NR1 by HVJ-liposome vector induces deficit of prepulse inhibition but not of spatial memory

Neurosci Res. 2003 Apr;45(4):473-81. doi: 10.1016/s0168-0102(03)00012-9.

Abstract

Considerable evidence suggests that an N-methyl-D-aspartate (NMDA) receptor plays a crucial role in memory and cognitive function. To identify the role of this receptor in higher functions of the brain, we delivered antisense oligonucleotides against an NMDA-NR1 subunit (NR1) to the hippocampus in rats using the HVJ-liposome-mediated gene-transfer method. NR1 hippocampal knockdown was performed by the focal injection of the NR1 antisense-HVJ-liposome complex into the bilateral hippocampus. The blocking effect of NR1-antisense on the expression of NR1 was confirmed by Western blot analysis. Spatial memory was tested by a water maze task, and sensorimotor gating was examined by prepulse inhibition (PPI). Western blot analysis demonstrated that the NR1-antisense treatment specifically provided the down-regulation (about 30%) of NR1 protein levels in the hippocampus. The water maze task showed that the antisense treatment did not affect spatial memory, while the PPI test revealed that NR1 hippocampal knockdown caused a deficit in sensorimotor gating. We conclude that mild dysfunction of hippocampal NMDA receptor causes sensorimotor gating deficit and relatively intact in spatial memory.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Animals, Genetically Modified
  • Down-Regulation
  • Gene Transfer Techniques
  • Gene Transfer, Horizontal
  • Genetic Vectors
  • Hippocampus / physiology*
  • Injections, Intraventricular
  • Liposomes
  • Male
  • Maze Learning / physiology*
  • Memory / physiology*
  • Motor Activity / genetics
  • Motor Activity / physiology*
  • Oligonucleotides, Antisense / administration & dosage
  • Rats
  • Rats, Wistar
  • Receptors, N-Methyl-D-Aspartate / genetics*
  • Receptors, N-Methyl-D-Aspartate / metabolism
  • Sendai virus / genetics
  • Thionucleotides / genetics

Substances

  • Liposomes
  • NMDA receptor A1
  • Oligonucleotides, Antisense
  • Receptors, N-Methyl-D-Aspartate
  • Thionucleotides