T-Maze Rewarded Alternation

Overview

The T-maze rewarded alternation task combines spatial working memory demands with appetitive motivation by placing food rewards in the goal arms according to an alternation rule. On the sample run, both goal arms are baited but only one is accessible; after the animal consumes the reward, it is returned to the start and given a free choice. The previously visited arm is now empty while the alternative arm still contains food, so correct alternation is reinforced by reward. This procedure leverages both the innate tendency to alternate and the learned association between novel-arm entry and reward, producing robust baseline performance that is highly sensitive to pharmacological or genetic disruption.

Performance is measured as the percentage of correct rewarded choices across trials, with secondary measures including choice latency, running speed, and reward consumption time. Food-motivated protocols have the advantage of generating consistent high-baseline performance (85-95% correct in well-trained animals), which provides ample dynamic range for detecting drug-induced impairments. However, they require food restriction to 85-90% free-feeding body weight and several days of pretraining to habituate animals to the maze, the reward, and the running procedure.

ConductMaze integrates automated reward detection through pellet sensors and lick-contact circuits in each goal arm, enabling real-time confirmation that the animal has consumed the reward before triggering the next phase. The software manages the alternation rule, logs reward collection times, and adjusts pseudorandom sample arm sequences to prevent side biases. Body weight tracking and food restriction schedules can be managed through the integrated colony management module.

Trial Flow

start

Arm Baiting

Both goal arms are baited with food reward; one arm is blocked by a guillotine door.

input

Sample Run

Animal runs from start to the open goal arm and consumes the reward.

decision

Reward Verification

Pellet sensor confirms reward consumption before trial advances.

process

Return & Delay

Animal is returned to the start compartment for the inter-trial interval.

input

Choice Run

Both arms open; previously visited arm is now empty, alternative arm retains reward.

output

Choice Scoring

Entry into the rewarded (novel) arm = correct; entry into the empty arm = error. Latency and speed recorded.

end

Session End

Session terminates after the configured number of trials; data are exported and maze cleaned.

Parameters

ParameterTypeDefaultDescription
Number of Trialsinteger10Number of sample-choice trial pairs per session.
Reward Typeenumsucrose-pellet-45mgType and size of food reward placed in each goal arm.
Inter-Trial Intervalduration15sDelay between reward consumption and start of the next trial.
Choice Phase Timeoutduration120sMaximum time allowed for the animal to make a choice before the trial is aborted.
Sample Arm SequenceenumpseudorandomForced arm sequence with no more than 3 consecutive same-side assignments.
Food Restriction Targetpercentage85%Target body weight as a percentage of free-feeding weight during testing.
Pretraining Daysinteger5Number of days of maze habituation and reward familiarization before testing.
Stem Lengthdistance60cmLength of the start arm from start position to the choice point.
Arm Lengthdistance30cmLength of each goal arm from choice point to reward location.

Metrics

MetricUnitDescription
Correct Choice %%Percentage of trials in which the animal chose the rewarded (novel) arm.
Mean Choice LatencysAverage time from start door opening to goal arm entry on choice runs.
Mean Running Speedcm/sAverage speed during the choice run from start to goal arm entry.
Reward Collection TimesAverage time from arm entry to pellet sensor activation indicating consumption.
Side Bias IndexratioProportion of left versus right choices, independent of correctness.
Perseverative ErrorscountNumber of consecutive errors to the same side, indicating rigid response patterns.
Trials to CriterioncountNumber of trials to reach a criterion of 8/10 correct consecutive choices.

Sample Data

SubjectGroupCorrect %Mean Latency (s)Running Speed (cm/s)Perseverative Errors

Representative data for illustration purposes. Actual values will vary by species, strain, and experimental conditions.

Applications

  • 1
    Anxiolytic Side EffectsDetecting cognitive impairment caused by benzodiazepines and other anxiolytic compounds at therapeutically relevant doses.
  • 2
    Motivational Confound ControlUsing reward-motivated performance to distinguish true memory deficits from motivational or motor impairments.
  • 3
    Learning Curve AnalysisTracking the acquisition of rewarded alternation across training days to assess procedural learning in addition to spatial memory.
  • 4
    Genetic Model CharacterizationPhenotyping transgenic mice for hippocampal-dependent spatial memory deficits with high baseline performance providing sensitive detection.

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