The aim of this study was to assess the effects of specific regimens of enrichment on the behaviour of C57BL/6J mice in the elevated plus-maze test (EPM). A total of 192 male C57BL/6J mice were allocated randomly to 32 cages. Three different items of cage furniture (CF) made of aspen — a mouse corner, nestbox and stairs — were added stepwise to different cages at intervals of one week so that the mice were exposed to an item of CF for one, two, three or four weeks. On the fifth week, all the mice were subjected to the EPM test. Overall, the presence of the nestbox or stairs for the three weeks appeared to have an anxiolytic effect on the behaviour of the mice, as evidenced by an increase in the number of entries made into the open arms and the time spent in the open arms of the EPM. The effects of these items of CF on the behaviour of the mice depended on the item used and on the duration of exposure. The items of CF that were used in this study appeared to improve the quality of life of C57BL/6J mice, as assessed using the EPM.

Serotonin 2C receptor (5-HT2CR) agonists attenuate reinstatement of cocaine-seeking behavior. These receptors are found throughout the limbic system, including the basolateral amygdala (BlA), which is involved in forming associations between emotional stimuli and environmental cues, and the central amygdala (CeA), which is implicated in the expression of conditioned responding to emotional stimuli. This study investigated whether 5-HT2CRs in the amygdala are involved in cue and cocaine-primed reinstatement of cocaine-seeking behavior. Rats were trained to self-administer cocaine (0.75 mg/kg, i.v.) which that was paired with light and tone cues, and then subsequently they underwent daily extinction training. Rats then received bilateral microinfusions of the 5-HT2CR agonist CP809101 (0.01–1.0 μg/0.2 μl/side) into either the BlA or CeA prior to tests for cue or cocaine-primed (10 mg/kg, i.p.) reinstatement. Rats were also tested for CP809101 effects on anxiety-like behavior on the elevated plus-maze (EPM). Surprisingly, intra-BlA CP809101 had no effect on cue reinstatement, though it did increase anxiety-like behavior on the EPM. Intra-CeA infusions of CP809101 attenuated cocaine-primed reinstatement, an effect that was prevented with concurrent administration of the 5-HT2CR antagonist SB242084 (0.1 μg/0.2 μl/side). CP809101 had no effect on cue reinstatement or anxiety-like behavior on the EPM. These findings suggest that 5-HT2CRs in the BlA modulate anxiety, whereas those in the CeA modulate incentive motivational effects induced by cocaine priming injections.