LAUSR

&NA; Increases in medial prefrontal cortex ERK have been linked to learning and memory processes. In the present study separate groups of rats initially underwent testing in an open‐field paired with either 2.0 mg/kg apomorphine or vehicle injections. Subsequently, in a brief conditioning 5 min. test the paired apomorphine group manifested a conditioned hyperactivity response. The vehicle/apomorphine groups were then subdivided into two vehicle and two apomorphine subgroups matched for their activity scores in this conditioning test. Following another apomorphine/vehicle pairing in the test environment the groups received 3 additional 5 min. non‐drug conditioning tests in which the groups received post‐trial vehicle/apomorphine treatments. The vehicle groups received vehicle either immediately or 15 min. after the first two of the three conditioning tests and the apomorphine groups received 2.0 mg/kg either immediately or 15 min. after the first two of the three conditioning tests. In the first conditioning test both of the apomorphine groups exhibited equivalent conditioned responses. By the third test, the conditioned response of the immediate post‐trial apomorphine group remained robust whereas conditioned response of the 15 min. apomorphine post‐trial group was extinguished. Immediately following the third conditioning test, the animals were euthanized and ERK was measured in the medial prefrontal cortex and the nucleus accumbens. ERK was enhanced in both brain areas, selectively in the immediate apomorphine post‐trial group. Increased ERK activity linked to the presence of the apomorphine conditioned response coupled with the absence of increased ERK activity following extinction of the apomorphine conditioned response suggests that ERK activity immediately following a conditioning test is an indicator of activity in brain systems with substantial dopaminergic input that are important in learning and memory. The facilitative effects of the immediate post‐trial apomorphine treatment on the conditioned response are also consistent with the proposition that immediate post‐trial dopaminergic drug treatments can modify the re‐consolidation of conditioned behavior. HighlightsImmediate post‐trial apomorphine treatments maintain an apomorphine conditioned response.An apomorphine conditioned response undergoes extinction when the post‐trial apomorphine injections are delayed by 15 min.An apomorphine conditioned response evokes an ERK response in dopamine target areas but not an extinguished response.