Journal
PSYCHOPHARMACOLOGY
Volume 232, Issue 14, Pages 2619-2629Publisher
SPRINGER
DOI: 10.1007/s00213-015-3897-y
Keywords
Amygdala; Contextual fear conditioning; Dopamine; D1 receptor; Hippocampus; Locomotor activity; Memory; Retrieval; Reconsolidation; Shock sensitivity
Categories
Funding
- BBSRC UK
- Leverhulme Trust
- University of Nottingham
- BBSRC [BB/J014982/1] Funding Source: UKRI
- Biotechnology and Biological Sciences Research Council [BB/J014982/1, 1363891] Funding Source: researchfish
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Dopamine D1-like receptor signalling is involved in contextual fear conditioning, but the brain regions involved and its role in other contextual fear memory processes remain unclear. The objective of this study was to investigate (1) the effects of SCH 23390, a dopamine D1/D5 receptor antagonist, on contextual fear memory encoding, retrieval and reconsolidation, and (2) if the effects of SCH 23390 on conditioning involve the dorsal hippocampus (DH) and/or basolateral amygdala (BLA). Rats were used to examine the effects of systemically administering SCH 23390 on the acquisition, consolidation, retrieval and reconsolidation of contextual fear memory, and on locomotor activity and shock sensitivity. We also determined the effects of MK-801, an NMDA receptor antagonist, on contextual fear memory reconsolidation. The effects of infusing SCH 23390 locally into DH or BLA on contextual fear conditioning and locomotor activity were also examined. Systemic administration of SCH 23390 impaired contextual fear conditioning but had no effects on fear memory consolidation, retrieval or reconsolidation. MK-801 was found to impair reconsolidation, suggesting that the behavioural parameters used allowed for the pharmacological disruption of memory reconsolidation. The effects of SCH 23390 on conditioning were unlikely the result of any lasting drug effects on locomotor activity at memory test or any acute drug effects on shock sensitivity during conditioning. SCH 23390 infused into either DH or BLA impaired contextual fear conditioning and decreased locomotor activity. These findings suggest that dopamine D1-like receptor signalling in DH and BLA contributes to the acquisition of contextual fear memory.
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