Subjective and Real Time: Coding Under Different Drug States.

Organisms are constantly extracting information from the temporal structure of the environment, which allows them to select appropriate actions and predict impending changes. Several lines of research have suggested that interval timing is modulated by the dopaminergic system. It has been proposed that higher levels of dopamine cause an internal clock to speed up, whereas less dopamine causes a deceleration of the clock.

Temporal maps in appetitive Pavlovian conditioning.

Previous research suggests animals may integrate temporal information into mental representations, or temporal maps. We examined the parameters under which animals integrate temporal information in three appetitive conditioning experiments. In Experiment 1 the temporal relationship between 2 auditory cues was established during sensory preconditioning (SPC).

Conditioned taste aversion from neostigmine or methyl-naloxonium in the nucleus accumbens.

An opioid antagonist injected in the nucleus accumbens of a morphine-dependent rat will lower extracellular dopamine and release acetylcholine (ACh), as also seen in opiate withdrawal. It was hypothesized that raising extracellular ACh experimentally would be aversive as reflected by the induction of a conditioned taste aversion. Rats were implanted with cannulas aimed above the nucleus accumbens (NAc) for injection of the opiate antagonist methyl-naloxonium in morphine-dependent animals or neostigmine to increase ACh in drug naïve animals.

Relative temporal representations in Pavlovian conditioning.

The transfer of relative temporal representations was assessed in a series of three experiments. In each experiment, rats (Rattus norvegicus) received one set of conditioned stimulus (CS) and intertrial interval (ITI) durations in Phase 1 and another set in Phase 2. The ratio between the CS and ITI intervals was either changed or maintained across phases.

Target-absent controls in blocking experiments with rats.

In three between-groups blocking experiments with rats, two concurrent and one forward, several common control procedures were employed: Reinforced trials with the putative blocking stimulus were either omitted entirely (Kamin control), replaced by unsignaled reinforcements (Wagner control), or replaced by reinforced trials with a different stimulus (C+ control). In each experiment, parallel treatments with the target stimulus absent during training served to examine the possibility that differential responding in tests with the target stimulus might be traced solely to differential exposure to the nontarget stimuli. In Experiment 1, responding by a concurrent blocking group during the test was no different than responding by a Kamin control group, and responding by a Wagner control group was greater than that of either of the other groups--a pattern of results, mirrored in the performance of the target-absent groups, that could be attributed to the elevation of contextual excitation by unsignaled reinforcement.

Amphetamine affects the start of responding in the peak interval timing task.

In this paper we investigate how amphetamine affects performance in a PI task by comparing two analyses of responding during peak trials. After training on 24 s fixed interval (FI-24) with 96 s peak trials, rats were given amphetamine for 4 consecutive days at doses of .5 and 1.