Comparison of automated video tracking systems in the open field test: ANY-Maze versus EthoVision XT

Charmaine J M Lim, Bettina Platt, Sanna K Janhunen, Gernot Riedel* (Corresponding Author)

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

3 Citations (Scopus)
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Abstract

BACKGROUND: ANY-Maze and EthoVision XT are two commonly used automated animal tracking systems employed to produce reliable and consistent results in behavioural paradigms. Data obtained with both tracking systems have presented differences, particularly when varying laboratory lighting conditions and contrasts of mice coat colour against the arena background in both water maze and tunnel maze.

METHOD: In this study, two fluorescent lighting conditions (58 and 295 lux), local to our laboratory, and different coat-coloured mouse lines (C57BL/6 J - black; CD1 - agouti; C3H/HeN - white) were used to compare reproducibility in measures of tracking systems (ANY-Maze versus EthoVision) in the open field test.

RESULTS: Differences between systems were reliant on the contrasts between coat and background colours. Surprisingly, black animals presented the greatest differences in read-outs between tracking systems, regardless of lighting conditions. Data from both video observation tools differed mainly in exploration-related parameters (distance travelled), but less in more static proxies (time in thigmotaxis zone). Overall, EthoVision XT returned higher values for most parameters analysed relative to ANY-Maze. More inconsistencies in recording and analysis can be expected from other video recording systems.

CONCLUSION: Data analysis software provides an additional source of variation in need of consideration when reproducibility in behavioural neuroscience is required.

Original languageEnglish
Article number109940
Number of pages13
JournalJournal of Neuroscience Methods
Volume397
Early online date9 Aug 2023
DOIs
Publication statusPublished - 1 Sept 2023

Bibliographical note

This project included funding from the Innovative Medicines Initiative 2/EFPIA, European Quality in Preclinical Data (EQIPD) consortium under grant agreement number 777364. We would also like to acknowledge the staff of the Medical Research Facility for their support with animal care, handling and behavioural experiments.

Data Availability Statement

All data are provided within the manuscript.

Keywords

  • video observation
  • animal tracking
  • mouse
  • light intensity

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