Left Lever Research Articles

Daily Rhythms in a Complex Operant: Targeted Percentile Shaping of Run Lengths in Rats

Daily rhythms in response output and accuracy were examined when reinforcement for a complex operant was uncoupled from accuracy of performance. Rats housed in operant conditioning chambers earned their daily ration of food under a targeted percentile procedure for responding on two levers. The targeted pattern was a series of consecutive responses on the left lever (a “run”), followed by a single response on the right lever. The targeted run length was either “0” (i.e., undefined, under the nondifferential baseline), 6, 12, or 24. Under baseline, a random third of all trials ended in pellet delivery; under the percentile conditions, trials with runs closer to the target than two-thirds of the runs from the most recent 24 trials ended in pellet delivery. This contingency shaped run lengths while ensuring that approximately one-third of all trials produced pellets. Responding tracked the target value well, with mean obtained run lengths equal to 90% of the target or better. Daily rhythms were clearly evident in measures of overall output, with subjects responding primarily 3–7 h into the dark period. The only substantial light-period responding observed in all subjects occurred during the 2 h after noon, when the chambers were serviced. No systematic variation in this pattern was observed as a function of target. Run length was much less variable across the daily cycle than was response output, with only a suggestion under the longest target that response accuracy was lower during periods removed from the period of peak activity.

Visuospatial Discrimination Deficit in Rats after Ibotenate Lesions in Anteromedial Visual Cortex

To assess the role of the rat anteromedial extrastriate cortex (AM) in a visuospatial discrimination task, restricted bilateral ibotenic acid lesions were placed stereotaxically in this region. Gray rats with lesions in AM were trained in a task requiring them to discriminate the location of a light stimulus placed vertically at different elevations. Correct responses required pressing right or left levers to obtain rewards. In contrast to unoperated controls, lesioned rats failed in learning the visuospatial discrimination task. A correlation was found between the bilateral extent of the lesion in area AM and the behavioral deficit. Another group of lesioned rats was trained to discriminate brightness differences of the light stimulus but requiring the same egocentric right/left motor response. The performance of these rats was similar to that of controls. From these results we conclude that extrastriate area AM in the rat is necessary for visuospatial discrimination, but not for correct egocentric motor responses. The visuospatial functions of area AM in the rat are reminiscent of visuospatial functions ascribed to the parietal streams of extrastriate visual areas in the monkey.

COMPARING LOCOMOTION WITH LEVER‐PRESS TRAVEL IN AN OPERANT SIMULATION OF FORAGING

An operant model of foraging was studied. Rats searched for food by pressing on the left lever, the patch, which provided one, two, or eight reinforcers before extinction (i.e., zero reinforcers). Obtaining each reinforcer lowered the probability of receiving another reinforcer, simulating patch depletion. Rats traveled to another patch by pressing the right lever, which restored reinforcer availability to the left lever. Travel requirement changed by varying the probability of reset for presses on the right lever; in one condition, additional locomotion was required. That is, rats ran 260 cm from the left to the right lever, made one response on the right lever, and ran back to a fresh patch on the left lever. Another condition added three hurdles to the 260‐cm path. The lever‐pressing and simple locomotion conditions generated equivalent travel times. Adding the hurdles produced longer times in patches than did the lever‐pressing and simple locomotion requirements. The results contradict some models of optimal foraging but are in keeping with McNair's (1982) optimal giving‐up time model and add to the growing body of evidence that different environments may produce different foraging strategies.

Intravenous self-administration of cocaine under concurrent VI schedules of reinforcement

Under concurrent VI (conc VI) schedules of reinforcement, organisms match the proportion of responses to the proportion of reinforcers obtained from the available options. This result is the basis of the matching law, a major theoretical view of the control of choice between and among available reinforcers. The present experiment examined the extent to which i.v. cocaine self-administration by monkeys under conc VI schedules of reinforcement was predicted by the matching law. One group of rhesus monkeys (n = 4) was prepared with chronic indwelling i.v. catheters and allowed to respond in a two-lever situation under conc VI schedules of reinforcement for cocaine injections. Three doses of cocaine (0.025, 0.05 and 0.1 mg/kg per injection) were made available under various conc VI schedules with an average inter-injection interval of 3 min. The same injection was available for each response, the difference between the options being the schedule of reinforcement. Each dose and schedule condition was in effect for at least ten consecutive sessions and until responding was stable. In a second group of monkeys (n = 3), a comparable experiment was conducted with responding maintained by the delivery of 1-g food pellets. Overall response rate maintained by cocaine was inversely related to dose. In addition, response rate decreased over the course of a session, apparently due to accumulation of cocaine. With regard to choice, more responding was maintained by the schedule that arranged more frequent injections. Choice was well predicted by the matching law, with a consistent tendency toward undermatching but no consistent bias toward one or the other option. Results were similar for behavior maintained by food, though two of three monkeys showed an unexplained bias toward the left lever. With regard to drug self-administration, these results demonstrate that in a choice situation, with all other variables being equal, injections that are available more frequently in time maintain behavior more strongly than less frequently available injections. Undermatching implies that the relative proportion of behavior maintained by the two options is somewhat less than the relative proportion of injections obtained. The finding that choice maintained by cocaine under conc VI schedules was comparable to choice maintained by food extends the generality of the conclusion that drugs and non-drug reinforcers control behavior by similar mechanisms.

Behavioral correlates of single units in the medial septal area: the effect of ethanol.

Experimental manipulations that compromise the medial septal area consistently and selectively impair working memory. The electrophysiological and pharmacological properties of medial septal neurons have been studied extensively, but the relation between medial septal neuronal activity and ongoing behavior has not been systematically analysed. Working memory was assessed in a continuous conditional discrimination task, and behavioral performance was correlated with medial septal single unit activity. Operant performance and the activity of rhythmically active neurons were continuously monitored during a 90 min test session, and peri-event time histograms of unit activity were constructed around relevant task events. Rats received intraperitoneal injections of either saline or ethanol (0.75 g/kg) 5 min before testing. Of the 52 medial septal neurons recorded under saline conditions, approximately 80% had significant behavioral correlates. Thirty-five per cent of these neurons were selectively activated at the time of the response and 65% at the time of the reward. Response-related activity was not selective for responses to the right or left lever, or to a particular type of trial, but in 61% of the cases was correlated with the accuracy of the response. In ethanol-treated rats, working memory was impaired, single unit activity was disrupted, and the behavioral correlates were less frequent and robust, especially the response-related correlates that were accuracy-sensitive. The results suggest that the medial septal area is involved in guiding accurate responses and processing rewards, and may contribute to the ethanol-induced impairments in working memory.

Effects of stimulation or blockade of central nicotinic-cholinergic receptors on performance of a novel version of the rat stimulus discrimination task.

This study evaluated the effects of two central nicotinic-cholinergic receptor agonists and an antagonist on performance accuracy of a rat, delayed stimulus discrimination task (DSDT). Rats were trained to discriminate between an auditory and visual stimulus by pressing a right or left lever. To diminish the rat's ability to use mediating spatial strategies to solve the task, computer automated, retractable doors separated the animal from the levers during delay intervals, thus reducing positioning at the lever. After stable baselines were achieved, rats were grouped and administered placebo (saline) and nicotine, lobeline or mecamylamine in a randomized dose series. Each group received two complete series of the selected compound on different occasions. Mecamylamine impaired DSDT accuracy in a dose-dependent manner while optimal doses of nicotine and lobeline significantly improved accuracy. Nicotine differed from lobeline in regard to its interaction with a dose of mecamylamine (1.0 mg/kg) that had not impaired DSDT accuracy. Combined administration of lobeline and mecamylamine was followed by a significantly increased level of DSDT accuracy that was similar to the improvement following administration of lobeline alone. In contrast, combined administration of nicotine and mecamylamine did not result in increased DSDT accuracy. Furthermore, lobeline administration similarly improved accuracy of trials associated with both the light and the tone, while nicotine improved accuracy of trials associated with the light to a much greater degree. These data suggest that the increases in DSDT accuracy associated with lobeline may be expressed through non-nicotinic mechanisms or a nicotinic receptor which is not blocked by mecamylamine.

Within-session patterns of responding when the operandum changes during the session

Eight pigeons and 10 rats responded on variable interval 1-min or variable interval 30-s schedules. During baseline, the same operandum produced reinforcers throughout the session. During the switch conditions, performing one response produced reinforcers early in the session and performing a different response produced reinforcers later. The switch between the two responses occurred 10, 20, 30, or 40 min into the session in different conditions. Within-session patterns of responding were not usually different when the same operandum produced reinforcers throughout the session and when the operandum changed from the right to the left key (pigeons) or lever (rats). Changes from a treadle to a key (pigeons) or from a lever to a key (rats) also failed to alter within-session patterns of responding. These results suggest that factors related to the form of the instrumental response (e.g., muscular warm-up, fatigue) contributed little to within-session changes in responding under the present circumstances.

Effects of different food-reinforcement histories on cocaine self-administration by rhesus monkeys

The purpose of the present study was to examine whether a history of responding under food reinforcement schedules that generated either high or low response rates would influence the acquisition and maintenance of cocaine self-administration. Eight experimentally naive rhesus monkeys were initially trained to respond on the right lever under either a fixed-ratio (FR) 50 or interresponse times (IRT) > 30-s schedule of food reinforcement. After 65 sessions of food-maintained responding, monkeys were surgically prepared with indwelling intravenous catheters and cocaine 0.03 mg/kg per injection (IV) was available on the left lever under a fixed-interval (FI) 5-min schedule. After at least 60 consecutive sessions at this dose, a cocaine dose-response curve (saline, 0.01-0.3 mg/kg per injection) was determined. The FR 50 schedule generated high rates of food-maintained responding (90.1 +/- 6.2 responses/min), while response rates under the IRT > 30-s schedule were low (1.9 +/- 0.1 responses/min). Across the 60 consecutive sessions under the FI 5-min schedule, linear changes in response rates and cocaine intake were significantly different between FR- and IRT-history monkeys. FR-history monkeys responded at higher rates than IRT-history subjects, while cocaine intake during the first 15 sessions was lower in FR- compared to IRT-history monkeys. Rates of cocaine-maintained responding after food-reinforcement histories were compared to response rates of monkeys initially trained to self-administer cocaine under an FI 5-min schedule (Nader and Reboussin 1994).(ABSTRACT TRUNCATED AT 250 WORDS)

Effects of nicotinic acetylcholine receptor ligands on behavioral vigilance in rats.

The effects of nicotinic receptor ligands on performance in a task measuring sustained attention, or vigilance, were tested. This task required the animals to discriminate between signal and non-signal events. The sequence of signal (central panel light illumination for 500, 50 or 25 ms) and non-signal presentations was randomized over three blocks of 54 trials each (27 signal trials, 9 per length, and 27 non-signal trials). A left lever press following a signal was counted as a hit, and a right lever press following a non-signal event was counted as a correct rejection. Hits and correct rejections were rewarded, whereas misses and false alarms (defined as incorrect right and left lever presses, respectively) were not. Baseline performance was characterized by a signal length dependent ability of the animals to discriminate between signal and non-signal events. Administration of nicotine (0.19, 0.62, 1.9 mumol) or of two novel nicotinic receptor agonists, ABT-418 and A-82695, did not produce main effects on vigilance performance. Lobeline (1.9, 6.2, 19 mumol), a nicotinic receptor ligand with mixed agonist/antagonist activities, impaired the animals' ability to discriminate between signal and non-signal events. The antagonist mecamylamine (5, 15, 50 mumol) potently impaired performance while increasing the number of errors of omission. The lack of effect of nicotine largely corresponds with the findings from previous studies on the acute effects of nicotine in intact subjects and non-smoking humans. While the detrimental effects of lobeline may have been related to the antagonist effects of this compound, the reasons for the differences between the effects of nicotine and lobeline still remain unsettled. These data support the hypothesis that nicotine receptor mechanisms are maximally activated in intact animals performing this task, and suggest that effects of acute nicotinic agonist treatment would not produce further cognitive benefit for these animals.

Learning new response sequences

Four rats were required to press either a right or left lever to complete various three-response sequences. After extended exposure to a training sequence, subjects were shifted to a new target sequence. The new target sequences always differed from the previous sequence by the response required in the first or last position of the sequence. Subjects were repeatedly exposed to all possible combinations of training and new target sequences. Learning of new sequences occurred more rapidly when the change in the new target sequence was in the last position. Errors persisted longer in new sequences in which the change was in the first position. Extinction of the training sequence occured faster when the change was in the last position. Responses in the last position were considerably more sensitive to the shift to new target sequences than were responses in the first position. Even though response sequences may form new behavioral units from the training sequence, reinforcement and extinction acted differentially on the individual lever presses within new target sequences rather than on the sequences as a whole. These findings support the hypothesis that response strength is determined by contiguity to reinforcement.

Prolonged Behavioral Effects of in Utero Exposure to Lead or Methyl Mercury: Reduced Sensitivity to Changes in Reinforcement Contingencies during Behavioral Transitions and in Steady State

Postnatal exposure to lead or methyl mercury results in mental retardation, learning deficits, and other neurobehavioral effects in humans, and adverse consequences of prenatal exposure have been clearly documented with methyl mercury. To examine the developmental neurotoxicity of these metals, especially lead, concurrent schedules of food reinforcement were used to identify learning deficits in squirrel monkeys exposed during gestation to either methyl mercury or lead. Pregnant squirrel monkeys were administered methyl mercury (0.7 to 0.9 ppm in maternal blood) or lead (21 to 79 μg/dl in maternal blood) during the last half to two-thirds of gestation. At about 5-6 years of age, offspring were trained to lever press under concurrent schedules of reinforcement in which separate random interval reinforcement schedules operated independently on two levers. Reinforcement densities were varied such that 20 to 90% of the reinforcers were programmed to derive from the left lever (i.e., one lever was "richer" than the other). At steady state, the behavior of the controls was sensitive to reinforcement density and showed little lever bias, but the behavior of monkeys exposed to more than 40 μg/dl of lead and to methyl mercury was less sensitive to reinforcement rates and heavily biased. When relative reinforcement density on a lever changed, the unexposed animals′ response rates gradually shifted to the newly rich lever. The behavior of monkeys exposed to methyl mercury or more than 40 μg/dl of lead changed slowly, not at all, or in the wrong direction. Steady-state behavior of monkeys exposed to less than 40 μg/dl resembled controls, but acquisition progressed more slowly and required 2-4 times as many reinforcers to complete. These effects suggest a behavioral mechanism-insensitivity to changing reinforcement contingencies-by which learning deficits and behavioral changes associated with these metals might be related to toxicant exposure. Since maternal blood levels corresponded to those that could be experienced in occupational settings, the present data raise the possibility of fetal hazards associated with maternal lead exposures at levels tolerated in humans in occupational settings.

Blocking Perturbations and Multilimb Control in Rapid-Aiming Movements

The effect of an unexpected mechanical block on the control of multilimb- aiming movements was studied in two experiments. In the first experiment, subjects (N = 10) attempted to push two hand levers 9 cm forward in 200 ms without vision. In the second experiment, subjects (N = 9) attempted to push hand levers and foot pedals forward 9 cm in 200 ms. After a practice period, five attempts at blocking the limb movements were made on the left lever and the right lever (Experiment 1) and on both levers (Experiment 2 only) during randomly selected trials. When one hand was blocked in Experiment 1, the other hand undershot the target on the first blocked trial, with slight reduc- tions in movement time. When one hand was blocked in Experiment 2, the contralateral limb undershot the target on all blocked trials, but this had little effect on the lower limbs. The lower limbs undershot the target when both up- per limbs were blocked. Discrete movement corrections were made on more of the blocked trials relative to...

In a low- versus high-dose drug discrimination task, random reinforcement in one drug state alters discriminative control only in that state1

This study investigated the effects of introducing random reinforcement training after a drug discrimination between 3.0 and 15.0mg/kg chlordiazepoxide had been acquired in rats; a two-lever food-rewarded operant procedure was used. Matched on the basis of dose-generalization test data, two dose-equisensitive groups were formed (A and B). Group A received 30 daily saline injections, which were followed by a random reinforcement session during which either left or right lever presses were reinforced on a probabilistic basis on each of the trials comprising a session. Group B received saline but no training or testing during this period. Subsequent testing revealed that responding conditioned to the low-dose training condition, but not to the high-dose training condition, was significantly changed in Group A. The randon reinforcement data further suggested that Group A did not discriminate saline from the low training dose. In Experiment 2, Group B of Experiment 1 was submitted to 30 random reinforcement training sessions, each preceded by a high training dose administration. Data showed that responding to the high dose, but not the low dose, was changed. For both experiments, chlordiazepoxide dose generalization following reacquisition was similar to that obtained before the random reinforcement phase. The findings indicate that the response pattern changed only for the stimulus condition present during random reinforcement. The random reinforcement manipulation did not disrupt the original discrimination between the high-and low-dose conditions.

Effects of amphetamine and nomifensine on intracranial self-stimulation discrimination behavior in rats

Rats implanted with electrodes in the medial forebrain bundle-lateral hypothalamus were trained in a discrete trial procedure to make a differential response (right or left lever press) in the presence or absence of brain stimulation [intracranial self-stimulation (ICSS)]. When animals reached a high level of accuracy (95% correct) in the discrimination task, testing was begun. In the first experiment, we compared the effects of saline and 0.3 mg/kg d-aphetamine when the intertrial interval (ITI) was 1, 5, 10, and 15 s. In the second experiment, animals were tested either with saline, 0.3 mg/kg d-amphetamine, or 1, 3, or 10 mg/kg nomifensine and the ITI was held constant at 5 s. Increasing the ITI from 1–15 s did not produce a drug-induced change in the discrminative stimulus properties of ICSS, although it did produce changes in total numbers of lever presses and numbers of intertrial lever presses. In the second experiment, neither d-amphetamine nor nomifensine altered the discriminative stimulus properties of ICSS, but a dose-response increase occurred in the time to complete the test session and in total number of lever presses and in presses on the initiating lever. Under conditions known to increase extracellular dopamine (DA) levels in brain, both amphetamine and nomifensine produced large increases in locomotor activity, but neither drug produced changes in the detection threshold for ICSS. Results indicated that the internal cues produced by ICSS are different from those produced by these psychomotor stimulant drugs.

CONTROL OVER RESPONSE NUMBER BY A TARGETED PERCENTILE SCHEDULE: REINFORCEMENT LOSS AND THE ACUTE EFFECTS OF d‐AMPHETAMINE

Two fixed-consecutive-number-like procedures were used to examine effects of acute d-amphetamine administration on control over response number. In both procedures, rats were required to press the left lever at least once and then press the right lever to complete a trial. The consecutive left-lever presses on each trial comprised a "run." Under the targeted percentile schedule, reinforcement was provided if the current run length was closer to the target length (16) than half of the most recent 24 runs. This differentially reinforced run length while holding reinforcement probability constant at .5. A second group acquired the differentiation under the targeted percentile schedule, but were then shifted to a procedure that yoked reinforcement probability by subject and run length to that obtained under the targeted percentile schedule. The two procedures generated practically identical control run lengths, response rates, reinforcement probabilities, and reinforcement rates. Administration of d-amphetamine disrupted percentile responding to a greater degree than yoked control responding. This disruption decreased reinforcement frequency less in the former than the latter procedure. The similar baseline responding under these two procedures suggests that this difference in sensitivity was due to behavioral adjustments to drug prompted by reduction of reinforcement density in the yoked control but not the percentile schedule. These adjustments attenuate the drug's effects under the former, but not the latter, procedure.

Safety signal withdrawal: a behavioural paradigm sensitive to both “anxiolytic” and “anxiogenic” drugs under identical experimental conditions

A new method involving the blockade of operant behaviour induced by the withdrawal of a conditioned signal for safety without presentation of a punishment signal has been developed for studying drugs with anxiolytic or anxiogenic properties. For this purpose, rats were trained under two alternating components of a multiple schedule of reinforcement FR8 (food)/FR1 (food) + RR 50% (shocks randomly delivered with 50 +/- 15% of the presses). The nonpunished and punished periods were signalled by one cue light above the right lever (safety signal) or the left lever (punishment signal), respectively. On the test session (safety signal withdrawal), the safety signal was turned off at the end of the first nonpunished period, but the punishment signal was not presented (every press was food rewarded and no shocks were delivered). During this period (4 min), rats exhibited a strong blockade of responding that lessened over time. This suppression seemed not to be caused by intervening events such as novelty, temporal conditioning, schedule of food delivery or ambiguity of the signal presented. The behavioural blockade induced by withdrawal of the safety signal was reduced by benzodiazepines: diazepam (0.5-4 mg/kg), chlordiazepoxide (4-8 mg/kg), nitrazepam (0.25-2 mg/kg), alprazolam (0.25-1 mg/kg), and partial agonists at benzodiazepine receptors: bretazenil (0.125-8 mg/kg) and ZK 91296 (32-64 mg/kg). Various 5-HT-related drugs also lessened the behavioural blockade:pCPA (3 x 150 mg/kg) and the 5-HT1A receptor agonists, buspirone (0.25-2 mg/kg), gepirone (0.25-1 mg/kg) but not 8-OH-DPAT. Compounds that may cause anxiety in humans further enhanced the blockade of lever pressing induced by the safety signal withdrawal at doses that did not modify baseline responding: d-amphetamine (0.125-0.5 mg/kg), caffeine (16 mg/kg) and picrotoxin (1 mg/kg). FG 7142 (8 mg/kg) and CGS 8216 (2-8 mg/kg) decreased responding during both components of the session. Therefore, the present paradigm seems sensitive to both "anxiolytic" and "anxiogenic" effects of drugs under identical procedural conditions.

Visual and auditory delayed discriminations in male and female Wistar rats

Different groups of male and female Wistar rats were exposed to a discrete-trial delayed discrimination procedure, in which subjects were required to discriminate between a continuously or intermittently presented visual (half of the subjects) or auditory (other half of the subjects) stimulus. The opportunity to respond was delayed for 0, 5, 10 or 20 s after stimulus presentation. Both response levers were inserted into the experimental chamber immediately upon the termination of the delay interval. A press on the left lever was followed by food if the continuous stimulus had been presented, while food was presented following a press on the right lever if the intermittent stimulus had been presented. During sessions 1–60, each incorrect response or failure to respond during the 5-s lever presentation was followed by presentation of the same visual or auditory stimulus, and the same delay interval, once the intertrial interval was terminated. This sequence was repeated until a correct response occurred. During sessions 61–90, repeated presentations of the same trial following incorrect responses or a failure to respond on initial trials were no longer presented. All other experimental contingencies remained unchanged. Response accuracy increased with prolonged training. Subjects exposed to the visual delayed discrimination procedure showed less accurate performance than subjects who were exposed to the auditory delayed discrimination procedure. Response accuracy was higher when the delay interval was short than when it was long. Males made more correct responses than females. However, significant sex by delay interval duration interaction effects were not observed, suggesting that sex differences in response accuracy cannot be attributed to sex differences in memory, but may rather result from sex differences in other, non-mnemonic processes.

On the limits of the matching concept in monkeys (Cebus apella).

Two cebus monkeys, with many years of experience matching a variety of static visual stimuli (forms and colors) within a standard matching-to-sample paradigm, were trained to press a left lever when a pair of displayed static stimuli were the same and to press a right lever when they were different. After learning the same/different task, the monkeys were tested for transfer to dynamic visual stimuli (flashing versus steady green disks), with which they had no previous experience. Both failed to transfer to the dynamic stimuli. A third monkey, also with massive past experience matching static visual stimuli, was tested for transfer to the dynamic stimuli within our standard matching paradigm, and it, too, failed. All 3 subjects were unable to reach a moderate acquisition criterion despite as many as 52 sessions of training with the dynamic stimuli. These results provide further evidence that, in monkeys, the matching (or identity) concept has a very limited reach; they consequently do not support the view held by some theorists that an abstract matching concept based on physical similarity is a general endowment of animals.

Interactions of diazepam and pentobarbital with RO 15–4513 on intracranial self-stimulation discrimination behavior in rats

Rats implanted with electrodes in the lateral hypothalamus were trained in a discrete trial procedure to make a differential response (right or left lever press) in the presence or absence of brain stimulation. When a high level of accuracy (95% correct) was attained in the discrimination, testing with vehicle, RO 15–4513, diazepam (1.0–10 mg/kg), diazepam plus RO 15–4513 (1.0 mg/kg), pentobarbital (1.0–17.5 mg/kg) and pentobarbital plus RO 15–4513 began. Diazepam, at 10 mg/kg, disrupted the discrimination behavior, and it also decreased the total number of lever-presses and increased the time to complete the session. These effects were blocked by the coadministration of 1.0 mg/kg RO 15–4513. Pentobarbital produced effects similar to those of diazepam, but these effects were only reversed to a limited extent by RO 15–4513. By itself, however, RO 15–4513 also decreased the total number of lever presses and increased the time to complete the session. Results were consistent with our previous findings with alcohol and RO 15–4513, and supported the notion that diazepam and alcohol have some similar effects at the GABA-benzodiazepine receptor complex.

The acquisition of visual and auditory discriminations in male and female Wistar rats

Different groups of male and female Wistar rats were trained to discriminate between visual or auditory stimuli in a discrete-trial experimental procedure. Presentation of one of the two visual stimuli or one of the two auditory stimuli was immediately followed by a 5-s presentation of the two levers. A press on the left lever was followed by food if one stimulus had been presented, while food was presented following a press on the right lever if the other stimulus had been presented. Incorrect responses or failure to respond during level presentation was always followed by presentation of the same visual or auditory stimulus once the intertrial interval had again expired. This sequence was consistently repeated until a correct response occurred. Discrimination performance improved as training progressed. Acquisition of the visual and auditory discrimination did not differ between males and females, although males were more likely than females to respond effectively during repeated trials (those trials which were initially incorrectly completed or not completed at all). The results of the present experiment make it likely that behavioral differences between the sexes in other experimental procedures are not due to differences in sensory discrimination abilities.