Exact(53)
The animals were confined to one of two conditioning chambers for 30 min during each pairing session.
Behavioural procedures were conducted in standard operant conditioning chambers located inside sound-attenuating, ventilated cubicles (Med Associates, VT, USA).
Self-administration testing was conducted in standard operant conditioning chambers (Coulbourn Instruments, Allentown, PA) as described previously [32], [33].
Testing was conducted in standard operant conditioning chambers (Coulbourn Instruments, Allentown, PA) enclosed in ventilated, sound-attenuating cubicles.
Testing for cued conditioning was conducted in rectangular conditioning chambers (Med-Associates, St . Albans VT) with white Plexiglas floors, situated in sound attenuating cubicles.
The two chambers were separated by a small sized holding chambers which also served as the partition between the two conditioning chambers.
Similar(7)
Mice were then returned to the conditioning chamber under conditions identical to day 1.
2 days later, mice were subjected to immediate shock in the conditioning chamber and their conditioned fear memory was tested 1 day after immediate shock.
SF1-ablated and control mice were placed in a conditioning chamber (Med Associates) and fear conditioned as previously described (Haubensak et al., 2010).
Approximately 24 h after conditioning, mice were exposed to the same conditioning context (identical conditioning chamber and odor cue) under drug-free conditions.
Cnp+/− mice showed higher percentage of freezing in the fear conditioning chamber already at baseline, that is before measurement of conditioned or cued memory (p = 0.007; Fig 2F), precluding the use of fear conditioning for memory assessment in these mice.
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