ConductVision · Behavioral Analysis

Zero Maze

Measure anxiety-like behavior on a circular elevated track with open and enclosed quadrants.

RodentAnxietyAuto Export
ConductVision / Zero Maze
Recording / Trial 3subject tracked
Open Time28%
Head Dips22
Distance5.6m

Key Parameters

Metrics automatically extracted by ConductVision.

24.3s

Time in Open Quadrants

Duration spent in unenclosed sections of the ring

24.3s

Time in Closed Quadrants

Duration spent in walled sections

Open Quadrant Entries

Number of transitions into open sections

Head Dips

Exploratory head movements over the edge of open quadrants

Distance Traveled

Total path length around the ring

Stretch-Attend Postures

Risk-assessment behaviors at open-closed boundaries

+ 5 more parameters trackedShow all
24.3s

Latency to First Open Entry

Time from placement to first open quadrant entry

Open Quadrant Duration Ratio

Percentage of session time in open sections — primary anxiety index

Transition Zones

Time spent at open-closed boundaries reflecting risk assessment

Velocity

Mean angular movement speed around the ring

Freezing Episodes

Immobility bouts in open quadrants indicating acute fear

What is the Zero Maze?

The Zero Maze (Elevated Zero Maze) is a circular variant of the elevated plus maze that eliminates the ambiguous center zone. The continuous ring has two open and two enclosed quadrants, providing a cleaner measure of approach–avoidance conflict in anxiety research.

ConductVision tracks the animal's angular position on the ring in real time, automatically scoring open vs. closed quadrant occupancy without the confound of center-zone dwell time inherent in plus-maze designs.

Protocol Parameters

ParameterDescriptionDefault
Ring Outer DiameterOuter diameter of the circular track60 cm (mouse) / 105 cm (rat)
Track WidthWidth of the running surface5 cm (mouse) / 10 cm (rat)
Wall HeightHeight of enclosed quadrant walls15 cm (mouse) / 27 cm (rat)
ElevationHeight above the floor40 cm (mouse) / 70 cm (rat)
Open/Closed RatioProportion of track that is open vs enclosed50/50 (2 open, 2 closed)
Test DurationStandard session length5 min
Light IntensityOverhead illumination300 lux
Start PositionAnimal placement at trial startClosed quadrant, facing wall
Quadrant EntryCriterion for scoring a quadrant entryAll four paws

Interpreting Results

Decreased Open Quadrant Time

Elevated anxiety — avoidance of unprotected sections, enhanced in chronic stress models and anxiogenic drug conditions.

Increased Open Quadrant Entries

Anxiolytic effect — more frequent transitions into open sections after diazepam (1–2 mg/kg) or chronic SSRI treatment.

Reduced Head Dips

Suppressed risk assessment — fewer exploratory dips over the edge from open quadrants indicates heightened anxiety.

Increased Stretch-Attend Postures

Cautious exploration — body elongation at boundaries without full entry reflects ambivalent approach-avoidance.

Reduced Distance Traveled

Sedation or freezing — overall hypolocomotion must be dissociated from genuine anxiety effects.

Prolonged Latency to First Open Entry

Initial anxiety — delayed first approach to open quadrants; sensitive to acute anxiogenic challenges.

Research Applications

Anxiety Research

  • Anxiolytic screening — eliminates center zone ambiguity of the elevated plus maze
  • Chronic stress — social defeat and restraint stress effects on open quadrant avoidance
  • Ethological measures — head dips and SAPs provide richer behavioral profiles than EPM

Pharmacology

  • Benzodiazepine dose-response — diazepam, chlordiazepoxide anxiolytic validation
  • Novel anxiolytics — CRF1 antagonists, neuropeptide Y agonists, and GABA modulators
  • Withdrawal states — ethanol and benzodiazepine withdrawal anxiety assessment

Genetic & Circuit

  • Transgenic models — 5-HT1A, CRHR1, and GABA receptor subunit knockout anxiety phenotyping
  • Optogenetic circuit dissection — BLA-CeA and vHPC-mPFC pathway contributions to anxiety
  • Strain comparisons — zero maze avoids center-zone confound across inbred strains

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