Repeated exposure to drug-associated cues without reward (extinction) leads to refraining from drug seeking in rodents. We determined if refraining is associated with transient synaptic plasticity (t-SP) in nucleus accumbens shell (NAshell), akin to the t-SP measured in the NAcore during cue-induced reinstatement of drug seeking. Using whole cell patch electrophysiology, we found that medium spiny neurons (MSNs) in NAshell expressed increased ratio of AMPA to NMDA glutamate receptor currents during refraining, which normalized to baseline levels by the end of the 2-hour extinction session. Unlike t-SP observed in NAcore during reinstated drug seeking, neither dendrite spine head enlargement nor activation of matrix metalloproteases (MMP2/9) accompanied the increased AMPA:NMDA in NAshell during refraining. Refraining was also not associated with changes in paired pulse ratio, NMDA receptor current decay time, or AMPA receptor rectification index in NAshell MSNs. Our preliminary data in transgenic mice suggest that t-SP may increase D2-MSN inputs relative to D1-MSN inputs.
Bibliographical noteFunding Information:
This work was supported by US Public Health Service grants DA038893, DA012512, DA003906, DA015369, GM008716, and TR000061. In these experiments, animals experienced cocaine self-administration followed by extinction training in the same context. This work was supported by US Public Health Service grants DA038893, DA012512, DA003906, DA015369, GM008716, and TR000061.
© 2019 Society for the Study of Addiction
PubMed: MeSH publication types
- Journal Article
- Research Support, N.I.H., Extramural