A Modified Barnes Maze for Juvenile Rats

Materials and Reagents

1. Nontoxic permanent markers, primary colors 
2. Scoop
3. Expanded polystyrene foam (Purchased from The Home Depot, Cellofoam^®, catalog number: 150705) 
4. 50 ml Falcon tube (Thermo Fisher Scientific, Falcon^® 50 ml Conical Centrifuge Tubes, catalog number: 14-432-22) 
5. Paper towels (Kimberly-Clark Professional*, Scott^® C-Fold Towel, catalog number: 06041)
6. 1 ml syringe or Pasteur pipette (Thermo Fisher Scientific, BD Lo-Dose^TM U-100 Insulin Syringes, catalog number: 14-826-79) 
7. Long Evans Rats (Original breeders purchased from Charles River Laboratories and bred at an AAALAC accredited animal facility, 17 to 25 days of age)
8. 500 ml 70% ethanol solution in an LDPE spray or squirt bottle (4-liter ethanol [Anhydrous] purchased from Thermo Fisher Scientific, catalog number: A405P-4)
9. Soy-based infant formula (22 oz purchased from Walmart, Enfamil^TM ProSobee Soy Infant Formula, catalog number: 2667028) 
10. Distilled water (150 ml to mix with ethanol and ~40 ml to mix with soy formula)
11. Examination gloves (Thermo Fisher Scientific, Fisherbrand^TM Powder-Free Nitrile Exam Gloves, catalog number: 19-130-1597C)
    

Equipment

1. Brightly lit testing room (3.6 x 5.25 m with a biosafety hood, overhead fluorescent lamps and two standing floor lamps with adjustable brightness on the highest setting) (Figure 1A)
2. Barnes maze apparatus (Figure 1B)
   
   1. Circular platform (wood coated with clear resin, 1.2 m in diameter) with eight equally spaced holes (10 cm in diameter) along perimeter 5 cm from platform edge (Resin purchased at The Home Depot, Rust-Oleum Parks^®, Gloss Super Glaze Interior Finish and Preservative, model: 241352)
   2. PVC platform stand elevated 0.75 m off the ground with wooden base (Figure 1C)
   3. PVC escape box, 9.19 x 3.00 in (Madesmart^®, catalog number: 59973) (Figure 1D)
   4. Rotating bar attached under platform to hold the escape box and allow the goal location to be altered per litter (Figure 1E)
   5. Foam or bubble wrap on the floor below the maze to cushion potential falls (Figure 1F)
      
      
      
   
   Figure 1. Experimental setup for Barnes maze adapted for juvenile animals. A. Arrangement of behavioral testing room and analysis room. B-F. Images of adapted Barnes maze platform (B), PVC platform stand with wooden base (C), PVC escape box (D), rotating bar for escape box (E), foam cushion for potential falls (F).
   
   
3. White curtains with distinct patterns made of large geometric shapes to create four walls of visual cues around the maze, as well as keep the experimenter hidden during testing (Figure 2)
   
   
   Figure 2. Visual Cues for Barnes maze adapted for juvenile animals. A. White curtains with enlarged visual cues. B. Dimensions of visual cues from right to left: horizontal rectangle (163 x 25 cm), triangle (base = 55 cm, height = 64 cm), circles (diameter = 25 cm), vertical rectangle (25 x 147 cm), stripes (8 x 163 cm).
   
   
4. Overhead camera (1/3" CCD, 30 frames/s, Panasonic, model: WV-CP280-N)
5. PC computer 
6. Stopwatch
   

Software

1. Video software (ULead Video Studio, Corel)
2. TopScan Version 2.00, CleverSys
3. Microsoft Excel
   

Procedure

See Figure 3A for the outline of the whole procedure.

1. Prior to testing
   Assign each of the 8 escape holes a letter from A-H going clockwise. Assign an escape box to one of the maze holes and attach the escape box to the rotating arm positioned under this hole. Keep this position consistent for the remainder of training (Days 2-3). Assign four drop-off locations (start location 1-4) by dividing the maze equally into four quadrants (Figure 3B).
   
   
2. Exploration in dim lighting (Day 1)
   
   1. Place home cage in biosafety hood in the testing room for 15 min prior to maze exposure for habituation. With a sharpie, mark each animal a different color on the tail. 
   2. Set room lights to lowest intensity (~25 lux) and keep visual cues unaltered throughout all testing Days 1-4. Place bubble wrap or foam on the floor around the circumference of the maze to cushion any falls. There is no escape box for Day 1 exploration.
   3. Open ULead video software and focus camera for dim lighting. Ensure the maze is centered in the picture and evenly spaced from the edges of the room when viewed with the camera. 
   4. Clean the maze with 70% ethanol and allow 60 s to dry.
   5. Add one scoop (approximately 8.8 g) of soy infant formula powder to a 50 ml Falcon tube and fill with distilled water. Shake vigorously until formula has fully been dissolved. 
   6. Fill one syringe or pipette with ~1 ml mixed soy infant formula and scatter dime-sized droplets fairly equally around the entire face of the maze.
   7. Gently carry the animal to the platform and place it in the center of the maze apparatus. Allow the animal to explore for 15 min. Record the time between the releases of the animal and when the 15 min of exploration is up. If the animal falls, quickly place it back in the center of the maze and watch its movement to detect any injury.
      Note: If falls are frequent, a raised border (~1 cm high) made of a serpentine automotive belt or similar material can be installed around the maze edge. Similar inserts inside of maze holes can also be used.
   8. Clean the maze with 70% ethanol and replace mixed soy infant formula droplets for the next animal. Wipe gloved hands with 70% ethanol in between handling different animals for this and all subsequent steps.
   
   
3. Training (Days 2-3) (Figure 3E) (Video 1)
   
   
   
   Video 1. Training trial. (All procedures were performed in accordance with the regulations stated in the Guide for Care and Use of Laboratory Animals by the National Research Council and approved by the George Mason University Institutional Animal Care and Use Committee.)
   
   
   1. Set room lights to their highest intensity (~525 lux).
   2. Place the home cage in the biosafety cabinet and allow animals 15 min in the home cage for habituation prior to testing the first animal. Clean the escape box and maze with 70% ethanol.
   3. Training consists of 5 blocks, with each block containing 4 trials (a 6^th ‘refresher’ block will be administered after an immediate probe only on Day 3). The trials allow the animal 60 s to locate the escape box. The order of the four start locations varies randomly for each block, and remains consistent for all animals tested in the litter. Hold a stopwatch in one hand and place animal at the designated quadrant facing the center of the maze with its rear paws in line with the escape holes (Figure 3C). Immediately after placing the animal in the maze, move out of sight behind the curtain and observe the animal’s behavior on the video display. Record the time between the releases of the animal and when all four paws enter the escape box (Figure 3D). If the animal does not locate the escape box within 60 s, hold the scruff on the upper back of the animal and gently guide its front paws to the escape hole. Clean maze apparatus and escape box with 70% ethanol prior to each block. When the last animal has completed block 1, repeat with the first animal for block 2. For a single animal, the start of one block and the next block should be within 15 to 30 min. After completion of the 5 training blocks, begin the immediate probe.
   
   
4. Immediate probe (Days 2-3)
   
   1. The immediate probe is used to test the animal’s recall of the goal location after training.
   2. The immediate probe is a 60 s probe directly following the five blocks of training trials. After five blocks of training have been completed, remove the escape box from the platform. Assign a start location for the probe at one of the four start locations opposite to the escape box location (Figure 3B). For instance, if the escape box was positioned under hole ‘G’ during the training trials, the opposite is start location 2 (S2). Therefore, S2 would be assigned as the start location for the immediate probe. The same probe start location is used for all subsequent probe trials and remains consistent within each litter. Begin the probe by placing the animal at the designated start location and allow 60 s for the animal to explore the maze.
      
      
      Figure 3. Barnes maze procedure. A. Layout of experimental timeline. B. Maze platform with labeled start locations (S1-S4) and escape holes (A-H) going clockwise. C. Image of drop off at start location. D. Image of animal with all four paws inside the escape box, indicating the end of analysis. E. Trace images of a juvenile (P23-25) animal at the beginning of training Day 2 (untrained), end of training Day 3 (trained), and the 24-Hour Probe. The green arrow displays the release location, and the red star marks the goal location.
   
   
5. Refresher block (Day 3)
   Following the Day 3 immediate probe, a 6^th block (4 trials with an escape box exactly like blocks 1-5) is administered to reinforce learning. This is to ensure the animal is still motivated to find the escape location during the 24 HP on Day 4.
   
   
6. 24-Hour probe (Day 4) (Figure 3E)
   
   1. The 24-h probe is similar to the immediate probes but begins approximately 24 h after the start of the final training period and is used to assess long-term spatial memory.
   2. Turn lights to their highest intensity with no escape box present and allow the animal 60 s to explore the maze.

Data analysis

Dwell time, velocity, path length and distance to goal are analyzed using TopScan.

1. Create an Arena: this defines the informational region 
   
   1. Open TopScan Version 2.00.
   2. Open trial: On the top left, click on the video camera icon and select a training video file. One training session is needed to create the arena. Arenas can be reused if maze position is unaltered. 
   3. If the circular maze has been distorted, select the eye icon to reveal the ‘Image Distortion Correction’ box. Next to ‘Morphing Option:’ select ‘Scale Adjust H/V:’ and type the first number as the scale in the north and south direction of the platform and the second number as the east and west (for example: 50/45) and hit ‘Apply’. The maze should no longer be oval (Figure S1A).
   4. Under ‘Arena’ on the top menu, select ‘Enter arena design mode’. A toolbar with different shapes will appear.
   5. On the toolbar, use the single ‘point’ and ‘center based circle’ icon to create zones: 
      
      1. Outer circle: select the ‘circle’ design tool and create a circle from the center of the maze that covers the entire circular platform. Once done, select ‘Finish zone operation’.
         Note: The Outer and Inner circle will be discarded later on as they are templates to create the Octants.
         On the right hand ‘Arena Design’ box, under ‘zones’ there will be a new zone named ‘1 CircleCtr’ that is color-coded to match the arena. Every new zone will appear similarly in the order in which it was created (Figure S1B). 
      2. Inner circle: create a smaller circle within the Outer circle that nearly reaches the escape holes.
         Note: The Inner circle will be discarded later on.
         Select ‘Finish Zone Operation’ (Figure S1C).
      3. Octants: right-click the Outer circle and select ‘split circle’ to equally divide it into eight sections. Rotate the octants so that the escape holes are centered. Repeat this step using the Inner circle and rotate the inner octants to line up with outer octants. Select ‘Finish Split Circle’. The octants will be labeled ‘PieCtr’ under ‘Zones’ (Figure S1D).
      4. In the right hand ‘Arena Design’ box under ‘zones’, select the first two circles made (Outer and Inner circle named ‘1 CircleCtr’ and ‘2 CircleCtr’) and delete (Figure S1E).
      5. Escape Hole Center: Click on the ‘point’ design tool. With the right clicker, place a point at the center of the goal escape hole, then select “Set Point Position’ (a green point will appear). Select ‘Finish Point Operation’ when done (point will turn red). This will allow measurement of the distance from the escape hole for the Gallagher analysis (Figure S1F).
      6. In the ‘Arena Design’ box, select the ‘Calibrate’ button. Right-click on one edge of the maze platform and select ‘First Calibration Point’. Redo this step on the exact opposite side of the maze edge and select ‘Second Calibration Point’. Enter the calibration distance as the diameter of the maze (1,200 mm). Right-click and select ‘Finish Calibration’ when done. This will allow the computer to estimate distance on the maze (Figure S1G).
      7. Define Zones: Select ‘new’ in the ‘Arena Design’ box. An ‘Area Definition’ box will pop up. Check the zones and name them as shown: 
      1)
      ALL: Check every zone (Figure S1H).
      2)
      PERI: This defines the perimeter from the Inner circle and Outer circle. Check every Outer circle octant (PieCtr).
      3)
      CENTER: This defines the area within the perimeter. Select all the octants that make up the Inner circle of the maze. 
      4)
      (A-H): Individually check the two ‘PieCtr’ that make a single octant slice on the maze (this includes a part of the Perimeter and Center) and label according to the assigned hole letter A-H located in that octant (Figure S1I).
      
      8. Name the Arena according to litter and Select ‘Finish’ when done.
         
2. Set Background: defines where the animal is traced. 
   
   1. Fast-forward the video until the animal is alone in the maze at the beginning of the trial.
   2. In the top menu under ‘Background’, select ‘Generate Background’.
   3. Run background generator until animal disappears.
   4. Stop and select ‘Save Background’ under ‘Background’ in the top menu.
      Note: Background may be reused if maze is unaltered and software is able to properly trace the animal without background noise.
   5. Alternatively, a single frame of an empty maze taken from the same video used for analysis can be used as a background ('Set Frame to Background Image') option.
3. Set Arena: Check ‘Arena’ on the left and select arena from file.
4. Select ‘Event’. In the ‘Event Rule Settings’ click the ‘Stop Rules’ tab and select ‘Duration’ under ‘Available Rule List’. Type ‘60 sec’ in the ‘After Analysis Duration >’ box. This will stop analysis from running past 60 s (Figure S2A).
5. Press the play button on the top left corner, then stop immediately after the video displays the experimenter releasing the animal and the hand is completely out of the maze.
   Note: To prevent interference of experimenter's hand, clothing, or shadow with video tracking, instruct experimenters to quickly withdraw hand after releasing the animal and take a step backward away from the maze.
6. Check ‘Analyze’ (located above the Area and Background box), then click fast forward and allow the video to run until the animal reaches the escape box. For probe trials, allow 60 s of analysis.
7. Click on ‘Export’ under ‘Result’ on the left. Select ‘OK’ and save text files.
8. Exporting Bin File to Excel
   
   1. Click on ‘Proc’.
   2. In ‘Proc’, select ‘Move Distance’ and click ‘OK’. 
   3. Select ‘Velocity’ and click ‘OK’. 
   4. Select ‘Dis to Point’, ‘Add’ the escape hole point created in arena mode ‘1’ and select ‘OK’ (Figure S2B).
   5. Change ‘Bin Size’ to 1. This analyzes the distance to the point every 1 s.
   6. Select ‘Export Data’.
9. The Topscan output is used to quantify escape latency, path length, and maximum and mean velocity measurements. For probe trials, these measurements are calculated for the path to first goal nose poke (by finding when distance to goal center first drops < 10 cm, followed by visual confirmation on the video) as well as the whole 60 s trial. The % dwell time per octant is also taken directly from the Topscan output. A relatively shorter escape latency and path length to goal as well as a higher % dwell time per octant are all indicators of superior maze performance. For a more detailed description of how these measurements might relate to spatial navigation strategy and hippocampal integrity, see McHail et al. (2018).
10. Nose pokes are manually scored by counting the number of times an animal pokes its nose inside of a hole as viewed by overhead video. If the animal pokes its nose in a hole, withdraws it, and then pokes its nose in the same hole again, this counts as two nose pokes. Separate nose poke tallies are recorded before and after the first goal nose poke. The number of nose pokes prior to the first goal poke can be used to compute an error score, that might also be weighted based on the distance of these nose pokes from the goal. An example of this scoring system applied to a developmental study can be found in McHail et al. (2018).
11. Maze performance differences between rats older and younger than three weeks of age are reported in McHail et al. (2018).

Notes

1. All cues are extra-maze visual cues. To accommodate juvenile eyesight, visual cues should be larger in size relative to the visual cues used to test adult animals.
2. Rodents can track their own and other animals’ odor trails (Wallace et al., 2002). To control for confounding olfactory cues (Lavenex and Schenck, 1997), it is suggested to rotate the maze between blocks, while keeping the goal location fixed relative to the visual cues. The maze apparatus and escape box should be wiped with 70% ethanol prior to each block (Rosenfeld and Ferguson, 2014).
3. It is recommended to use background white noise, such as from an overhead ventilation system, to mask potential auditory cues.
4. It is recommended to test juvenile animals of the same age and cohort since performance can vary greatly at this stage of development (McHail et al., 2018). While sex differences were reported in adult rats in the Morris Water Maze (Roof and Stein, 1999), no sex differences were observed in the pre-pubertal rat performance on the Barnes maze (Ojeda and Urbanski, 1994; McHail et al., 2018).
   

Acknowledgments

This protocol was used in our previous study to analyze spatial navigation in juvenile rats (P17-P25) (McHail et al., 2018). The authors thank Richard H. Ogoe, Diyi Chen, Amir Behsudi and Celeste Chong for their technical support. This work was supported by the National Institutes of Health (NIH) National Institute on Aging (NIA) through Grant 1R15AG045820-01A1 and the Krasnow Institute for Advanced Study at George Mason University.

Competing interests

The authors declare that there is no conflict of interest.

Ethics

All procedures were performed in accordance with the regulations stated in the Guide for Care and Use of Laboratory Animals by the National Research Council and approved by the George Mason University Institutional Animal Care and Use Committee.

References

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