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Drug-paired contextual stimuli increase dendritic spine dynamics in select nucleus accumbens neurons
journal contribution
posted on 2023-06-09, 18:12 authored by Bryan SingerBryan Singer, Nancy Bubula, Dongdong Li, Magdalena M Przybycien-Szymanska, Vytautas P Bindokas, Paul VezinaRepeated exposure to amphetamine leads to both associative conditioning and non-associative sensitization. Here we assessed the contribution of neuronal ensembles in the nucleus accumbens (NAcc) to these behaviors. Animals exposed to amphetamine IP or in the ventral tegmental area (VTA) showed a sensitized locomotor response when challenged with amphetamine weeks later. Both exposure routes also increased ?FosB levels in the NAcc. Further characterization of these ?FosB+ neurons, however, revealed that amphetamine had no effect on dendritic spine density or size, indicating that these neurons do not undergo changes in dendritic spine morphology that accompany the expression of non-associative sensitization. Additional experiments determined how neurons in the NAcc contribute to the expression of associative conditioning. A discrimination-learning procedure was used to expose rats to IP or VTA amphetamine either Paired or Unpaired with an open field. As expected, compared to Controls, Paired rats administered IP amphetamine subsequently showed a conditioned locomotor response when challenged with saline in the open field, an effect accompanied by an increase in c-Fos+ neurons in the medial NAcc. Further characterization of these c-Fos+ cells revealed that Paired rats showed an increase in the density of dendritic spines and the frequency of medium-sized spines in the NAcc. In contrast, Paired rats previously exposed to VTA amphetamine showed neither conditioned locomotion nor conditioned c-Fos+ expression. Together, these results suggest a role for c-Fos+ neurons in the medial NAcc and rapid changes in the morphology of their dendritic spines in the expression of conditioning evoked by amphetamine-paired contextual stimuli.
History
Publication status
- Published
File Version
- Accepted version
Journal
NeuropsychopharmacologyISSN
0893-133XPublisher
Springer NatureExternal DOI
Issue
8Volume
41Page range
2178-2187Department affiliated with
- Psychology Publications
Full text available
- Yes
Peer reviewed?
- Yes