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Animal
Mouse, Rat

Conditioned Place Preference Cages for Rats or Mice - 2- or 3-compartment (CPP)

Product Code:42552/42553/42552-D03/42553-D03/43552-D03/43553-D03

The Conditioned Place Preference (CPP) test is a widely used behavioral paradigm for evaluating the motivational properties of rewarding or aversive experiences. Ugo Basile offers a complete family of CPP systems, including 2-compartment, 3-compartment, and versions for thetered animals, designed to provide researchers with maximum flexibility in evaluating the abuse potential of substances and the motivational effects of drugs in mice or rats.

Interchangeable floors, optimized for use with video-tracking software or visual scoring, thanks to the grey, high-contrast color and non-smooth, non-reflective paint.

Our systems use interchangeable tactile floors and visual wall patterns to create robust contextual cues. The three-compartment model includes a neutral central chamber, ideal as a starting point for unbiased testing. All models are fully optimized for use with video-tracking software or visual.

Model
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An extended warranty can be added for most Ugo Basile products. You can find this information in the ordering information section of each product.
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Background

  • The delivery of appetitive and addictive substances (e.g. drugs) or aversive and unpleasant ones in separated cages the animal should retain a memory of, and hence a preference is a classic and relatively simple experiment.
  • Scientists use the rewarding, aversive or even neutral floor and walls differences to create an expectation in the animals that it is in that compartment that they will get more, move more, groom or rear more, etc.
  • Obviously the different walls tend to have a weaker impact than floor texture on the association drug-reward-environment, as rodents have a poor visual sense and it’s normal that changing the floors (e.g. squared of different square size, circular holes, plastic, etc.) will be more effective in inducing a preference for one of the two sides with many potential and highly translational discoveries possible, eg:
    • Evaluate the addictive power of a drug (real or recreational)
    • Evaluate the positive effects of antagonist drugs, which may be real antidotes and save lives (e.g. Naloxone in Heroin overdoses)
    • Much more, including memory and conditioning

2-Compartment CPP

This classic configuration consists of two distinct chambers, separated by a door. Each chamber features unique tactile and visual cues.
During conditioning, animals are confined to one chamber after receiving the treatment. During the test session, access to both chambers is allowed and the time spent in each environment is measured to determine preference or aversion.

This design eliminates the interpretational complexity of a third chamber and provides a clear binary choice, making it ideal for straightforward CPP/CPA paradigms.

3-Compartment CPP (with Neutral Area)

The three-chamber apparatus adds a central neutral compartment, made of smooth, non-patterned plastic. Two doors connect the neutral area to the lateral conditioning chambers.
The neutral area and the time spent in it represent an additional parameter to be evaluated, which adds complexity to data interpretation.

2-Compartment CPP Vs. 3-Compartment CPP

The dilemma about the 2 or 3 compartment CPP test is a matter of deciding if:

  • Option 1: 2 chambers - Ease of protocol and objectivity in data interpretation with randomization of initial/treatment chamber.
  • Option 2: 3 chambers - The animal is put in the central zone as a neutral area, which can be useful as it gives a neutral starting point, however it also makes the analysis of the time spent in this 3

 Customizable, optimized for tracking

  • The box includes the contextual cues required by the experimental paradigm for the customizable compartments:
    • 4 interchangeable floors with square or circular patterns
    • 2 sets of walls, for the 2 experimental chambers
  • Designed and optimized for use with any video-tracking software (such as ANY-maze) or visual scoring.
  • Quick and easy to change both the floors and the wall contexts for a visual and tactile difference between the 2 compartments.
  • On request we can provide customized sets of walls, with different patterns or textures.
  • Works with cabled animals for optogenetics, electrophysiology, miniscopes, etc.

 

FeatureBenefit

Interchangeable patterned floors and walls

The two compartments differ by tactile stimulation

Walls in either compartment can be altered, by replacing the context kit

The two compartments differ by visual stimulation

High contrast with light or dark animals

Optimized for Video-Tracking

Specific models and floors for rats or mice

Designed for multiple-cage systems for high throughput

Physical

Animal42552/42552-D03 Rat (2-compartment)42553/42553-D03 Mouse (2-compartment)43552 Rat (3-compartment)43553 Mouse (3-compartment)

External Dimensions (handles excluded)

63x32x35(h)cm

35x18x29(h)cm  81x33x 32(h)cm 45,4 x16,2x32(h)cm

Internal Dimensions (lateral compartments)

30x30x30(h)cm 16x15x25(h)cm  30x30x30(h)cm 16x15x25(h)cm 
Internal Dimensions (central compartment) n.a. n.a. 10X30x30(h)cm 5X15x25(h)cm

Patterned Floors

4 interchangeable floors for each cage

4 interchangeable floors for each cage 4 interchangeable floors for each cage 4 interchangeable floors for each cage

Context Walls

2 interchangeable context kits provided with each cage (striped and checkered)

2 interchangeable context kits provided with each cage (striped and checkered) 2 interchangeable context kits provided with each cage (striped and checkered) 2 interchangeable context kits provided with each cage (striped and checkered)

Warranty

Warranty Conditioned Place Preference is covered by a 12-month warranty + 12 after product registration 

The CPP paradigm provides information on the rewarding or aversive effects of visible and tactile contextual cues associated with drugs.
This technique has acquired great popularity in research studies involving addiction, being much easier, if compared to drug self-administration procedures.

First, the animal is conditioned to identify one of the two compartments with the drug experience. Then the time spent in each compartments is measured; preference or
aversion to the drug-paired compartment, hence rewarding/aversive properties of drugs, can be easily deducted.

The CPP test only requires the animal to carry out a simple operation (i.e. move from one compartment to the other) to approach or avoid the drug-paired compartment; the animal is expected to spend more time in the drug-paired compartment, if the drug experience produced a positive effect.

The CPP paradigm provides information on the rewarding or aversive effects of visible and tactile contextual cues associated with drugs.

This technique has acquired great popularity in research studies involving addiction, being much easier, if compared to drug self-administration procedures. First, the animal is conditioned to identify one of the two compartments with the drug experience. Then the time spent in each compartment is measured; preference or aversion to the drug-paired compartment, hence rewarding/aversive properties of drugs, can be easily deducted. The CPP test only requires the animal to carry out a simple operation to approach or avoid the drug-paired compartment; the animal is expected to spend more time in the drug-paired compartment, if the drug experience produced a positive effect.

Ordering information

42552

Rat Cage for Conditioned Place Preference (CPP), including 4 interchangeable floors and 2 context kits

42552-D03 Rat Cage for Conditioned Place Preference (CPP), including 4 interchangeable floors and 2 context kits, for tethered animals

42553

Mouse Cage for Conditioned Place Preference (CPP), including 4 interchangeable floors and 2 context kits

42553-D03 Mouse Cage for Conditioned Place Preference (CPP), including 4 interchangeable floors and 2 context kits, for tethered animals

43552-D03

Rat Cage for Conditioned Place Preference (CPP), including 4 interchangeable floors and 2 context kits, with central neutral area and 2 doors to access the experimental chambers, for thetered and non-tethered animals.

43553-D03

Mouse Cage for Conditioned Place Preference (CPP), including 4 interchangeable floors and 2 context kits, with central neutral area and 2 doors to access the experimental chambers, for thetered and non-tethered animals

Back to: Behaviour, Conditioning, Reward

Research insights

Behavioural neuroscience and preclinical research

Understanding how animals learn, remember and respond to environmental stimuli is central to neuroscience research. Behavioural assays in this domain cover a wide range of constructs, including associative learning, memory consolidation, anxiety, fear extinction, social interaction, stress response, addiction and reward processing.

These paradigms are widely used in preclinical neuropharmacology, translational psychiatry and neuroscience research.

Most used paradigms for behavioural neuroscience, conditioning and reward studies

Behavioural neuroscience relies on a broad range of paradigms to study learning, memory, anxiety, fear, stress, social interaction, addiction and reward processing in rodents. Conditioning paradigms include fear conditioning, active avoidance, passive avoidance and operant conditioning, which are used to investigate associative learning, memory retention, avoidance behaviour, reinforcement learning and goal-directed responses.

Startle and prepulse inhibition (PPI) paradigms are used to assess sensorimotor gating and translational models related to neuropsychiatric disorders like schizophrenia. Maze-based paradigms, including Morris water maze, Barnes maze, Y-maze, T-maze, radial arm maze, elevated plus maze and light/dark box, support the study of spatial learning, working memory, reference memory, anxiety-related behaviour and exploratory decision-making.

Open-field, social interaction, conditioned place preference, self-administration and other reward-related paradigms can be combined with video tracking to quantify locomotion, exploration, freezing, thigmotaxis, preference, social behaviour and reward-driven responses.

Operant systems are also designed for the most common Skinner-like experiments or for very complex tasks like the Attentional Set-Shifting protocol, which mimics the Wisconsin Card Sorting (or Cantab) test in humans.

Key measured parameters and behavioural readouts

Behavioural neuroscience studies rely on readouts that quantify learning, memory, fear responses, avoidance behaviour, exploratory activity, sensorimotor gating, social interaction and reward-related behaviour. Key measured parameters include freezing behaviour, response latency, number of avoidances, number of non-responses, intertrial crossings, startle amplitude, prepulse inhibition, locomotor activity, distance travelled, time spent in specific zones, thigmotaxis, exploration patterns, social interaction metrics and reward-related responses across repeated sessions.

These readouts help researchers assess associative learning, memory consolidation, fear extinction, anxiety-related behaviour, sensorimotor gating, addiction, reward processing and cognitive performance in rodent models. Depending on the experimental paradigm, behavioural data may be collected through conditioning chambers, avoidance systems, startle/PPI platforms, operant setups, mazes, open-field arenas or video-tracking systems. The Ugo Basile portfolio includes Fear Conditioning, Startle/PPI, Active and Passive Avoidance, Operant Conditioning systems, mazes and tracking-compatible behavioural arenas.

Ugo Basile instruments for behavioural neuroscience, conditioning and reward studies

For more than 60 years, Ugo Basile has designed and manufactured instruments for behavioural neuroscience, combining classical paradigms with continuously updated technology.

The Fear Conditioning System is designed to assess cued and contextual fear memory through automated freezing detection, with sound-attenuating chambers, VIS/IR illumination and compatibility with tethered animals for advanced techniques such as optogenetics, electrophysiology and fiber photometry. The system can be expanded up to multiple chambers and can also be upgraded to Startle/PPI using the same cubicle and electronics.

The Startle PPI 3.0 system is used to measure sensorimotor gating in rodents through startle responses to pulses and prepulses, with flexible software-driven protocol design and dedicated mouse and rat platforms.

Ugo Basile also offers Operant Conditioning solutions for reinforcement learning, goal-directed behaviour and reward-based experimental paradigms.

For avoidance learning and memory, Ugo Basile provides Active Avoidance and Passive Avoidance systems. Active Avoidance allows researchers to measure avoidances, non-responses, response latency and intertrial crossings in shuttle-box paradigms, while Passive Avoidance is used to assess short- and long-term memory based on fear-motivated learning.

The Conditioned Place Preference (CPP) test is a widely used behavioral paradigm for evaluating the motivational properties of rewarding or aversive experiences. The CPP paradigm provides information on the rewarding or aversive effects of visible and tactile contextual cues associated with drugs.

Frequently Asked Questions

What behavioural paradigms are used in preclinical neuroscience?

Preclinical behavioural neuroscience uses a wide range of paradigms to study learning, memory, anxiety, fear, stress, reward, addiction, social behaviour and exploratory activity. Common paradigms include fear conditioning, active avoidance, passive avoidance, operant conditioning, startle and prepulse inhibition, open field, social interaction tests, conditioned place preference, Morris water maze, Barnes maze, Y-maze, T-maze and radial arm maze.