LTP in the mouse nucleus accumbens is developmentally regulated

Synapse. 2002 Sep 15;45(4):213-9. doi: 10.1002/syn.10104.

Abstract

Glutamatergic transmission in the nucleus accumbens (NAc) has been shown to be important for behavioral adaptations in response to drugs of abuse. NMDA-receptor dependent long-term potentiation (LTP) of glutamatergic synaptic transmission has been hypothesized to underlie many lasting alterations in behavior. Thus, we examined LTP in NAc core and find that it is developmentally regulated. Specifically, tetanus-evoked, NMDA receptor-dependent LTP is observed in the NAc of "adolescent" (3-week-old) mice more frequently than in adult (6-20-week-old) mice. In contrast, cAMP-dependent enhancement of transmission is not developmentally regulated. Removal of extracellular Mg(2+) restores LTP in adult NAc core, suggesting developmental regulation of induction processes rather than maintenance mechanisms. These findings are discussed in the context of behavioral changes elicited in response to drugs of abuse, which differ in adolescent vs. adult rodents and humans.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Age Factors
  • Animals
  • Colforsin / pharmacology
  • Cyclic AMP / metabolism
  • Electrophysiology
  • Evoked Potentials / physiology
  • Glutamic Acid / physiology
  • Long-Term Potentiation / physiology*
  • Magnesium / pharmacology
  • Male
  • Membrane Potentials / drug effects
  • Membrane Potentials / physiology
  • Mice
  • Mice, Inbred C57BL
  • Nucleus Accumbens / growth & development*
  • Nucleus Accumbens / physiopathology*
  • Organ Culture Techniques
  • Receptors, N-Methyl-D-Aspartate / physiology
  • Substance-Related Disorders / physiopathology
  • Synapses / drug effects
  • Synapses / physiology*

Substances

  • Receptors, N-Methyl-D-Aspartate
  • Colforsin
  • Glutamic Acid
  • Cyclic AMP
  • Magnesium