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Total Distance Traveled: A Quantitative Measure of Emotional and Motor Activity in the Elevated Plus Maze

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Why Distance Matters in the Elevated Plus Maze

The Elevated Plus Maze (EPM) is a cornerstone of behavioral neuroscience for studying anxiety-like responses in rodent models. Traditionally, researchers have focused on metrics such as time spent in open vs. closed arms and entry frequency. While these measures provide essential insight into exploratory behavior and risk aversion, Total Distance Traveled (TDT) offers a complementary yet distinct perspective—serving as a window into the subject’s global locomotor activity, internal arousal state, and pharmacological responsiveness.

Unlike arm-specific metrics, TDT reflects the summative behavioral output of the animal during the entire test session. At Conduct Science, our Elevated Plus Maze—paired with advanced tracking software like ConductVision or ANY-maze—delivers high-resolution locomotor data at 30+ frames per second, allowing for precise, reproducible quantification of distance metrics.

Defining Total Distance Traveled (TDT)

Total Distance Traveled refers to the aggregate length of all locomotor paths made by the animal during a typical 5–10 minute EPM session. It incorporates movement across open arms, closed arms, and the center zone.

While it may seem like a secondary measure, TDT can signal critical behavioral and physiological changes, including:

  • Hyperlocomotion (e.g., stimulant drug effect)
  • Motor suppression (e.g., sedative or sickness behavior)
  • Stress-induced freezing or hesitation
  • Habituation or fatigue across trials

Scientific Value of TDT in Behavioral Interpretation

1. Disambiguating Anxiety from Motor Effects

In pharmacological studies, elevated time in the open arms is often interpreted as an anxiolytic effect. However, without TDT, one cannot rule out sedative interference. For instance:

Observation Possible Interpretation
Low open arm time + low TDT
Anxiety or motor suppression
High open arm time + low TDT
Reduced anxiety or sedation?
High open arm time + high TDT
Anxiolysis with intact locomotion

Thus, TDT ensures behavioral interpretations are not confounded by impaired or exaggerated motor activity.

2. Identifying Behavioral Strategies

Rodents differ in how they approach the EPM task. Some prefer to stay close to walls and only make short trips; others may traverse arms freely. TDT offers a global measure of task engagement:

  • High distance, high open entries: Exploratory, low anxiety

  • High distance, low open entries: High anxiety with hyperactivity (e.g., ADHD models)

  • Low distance, high open entries: Anxiolysis with reduced drive

3. Monitoring Habituation and Longitudinal Changes

In repeated-exposure paradigms or aging models, a decline in TDT over sessions may signal habituation, motor decline, or waning exploratory motivation. This is especially useful when combined with metrics like time in arms or center zone visits.

Conduct Science EPM + ConductVision: Designed for Locomotor Precision

Our Elevated Plus Maze system supports high-fidelity behavioral tracking:

  • Modular arm design: Removable rails, height-adjustable

  • ConductVision AI software: 11-point body detection, no tagging required

  • High-speed tracking: 30+ fps video capture

  • Data outputs: Total path length, average speed, speed per zone, heatmaps, and behavioral annotations

Whether you’re studying neurodegeneration, pharmacology, or genetic mutations, these tools provide the granular distance data needed to parse behavioral complexity.

Sample Dataset: Assessing Distance Across Drug Conditions

In an experimental EPM study comparing the effects of a new GABAergic anxiolytic, researchers observed the following:

Group Time in Open Arms (s) Total Distance Traveled (cm) Avg. Speed (cm/s)
Vehicle Control
85.4 ± 6.2
990.8 ± 74.3
3.31 ± 0.28
Anxiolytic – Low
142.1 ± 9.7
1022.6 ± 65.2
3.44 ± 0.23
Anxiolytic – High
171.5 ± 10.3
803.5 ± 59.4
2.75 ± 0.18

The high-dose group showed greater open arm duration but lower total distance, indicating reduced anxiety paired with potential motor sedation—a distinction that would be missed without TDT.

When Should Researchers Prioritize TDT?

  • In pharmacological screening to distinguish side effects

  • In aging and neurodegenerative models to track movement decline

  • In neurodevelopmental studies (e.g., hyperactive or hypoactive phenotypes)

  • During longitudinal testing to capture behavioral adaptation or fatigue

TDT is especially helpful when movement itself is a behavioral endpoint—whether due to stress-induced freezing, hypervigilance, or drug-induced lethargy.

Conclusion: Time in the Open Arms as a Window into Anxiety

In behavioral science, we often interpret where an animal goes. But just as important is how much and how fast it gets there. Total Distance Traveled in the Elevated Plus Maze offers a quantitative, scalable, and high-resolution lens through which researchers can assess emotional, neurological, and pharmacological states.

With Conduct Science’s Elevated Plus Maze and ConductVision’s tracking power, every step an animal takes becomes meaningful, measurable, and reproducible.

Ready to enhance your anxiety research toolkit?

References

  • Pellow, S., et al. (1985). Validation of open:closed arm entries in an elevated plus-maze as a measure of anxiety in the rat. J. Neurosci Methods, 14(3), 149–167.
  • Rodgers, R.J. & Dalvi, A. (1997). Anxiety, defence and the elevated plus-maze. Neurosci. Biobehav. Rev., 21(6), 801–810.

Written by researchers, for researchers — powered by Conduct Science.

Author:

Louise Corscadden, PhD

Dr Louise Corscadden acts as Conduct Science’s Director of Science and Development and Academic Technology Transfer. Her background is in genetics, microbiology, neuroscience, and climate chemistry.