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In This Article

  • Summary
  • Abstract
  • Introduction
  • Protocol
  • Results
  • Discussion
  • Disclosures
  • Acknowledgements
  • Materials
  • References
  • Reprints and Permissions

Summary

This study presents an innovative running wheel-based animal mobility system to quantify an effective exercise activity in rats. A rat-friendly testbed is built, using a predefined adaptive acceleration curve, and a high correlation between the effective exercise rate and the infarct volume suggests the protocol's potential for stroke prevention experiments.

Abstract

This study presents an animal mobility system, equipped with a positioning running wheel (PRW), as a way to quantify the efficacy of an exercise activity for reducing the severity of the effects of the stroke in rats. This system provides more effective animal exercise training than commercially available systems such as treadmills and motorized running wheels (MRWs). In contrast to an MRW that can only achieve speeds below 20 m/min, rats are permitted to run at a stable speed of 30 m/min on a more spacious and high-density rubber running track supported by a 15 cm wide acrylic wheel with a diameter of 55 cm in this work. Using a predefined adaptive acceleration curve, the system not only reduces the operator error but also trains the rats to run persistently until a specified intensity is reached. As a way to evaluate the exercise effectiveness, real-time position of a rat is detected by four pairs of infrared sensors deployed on the running wheel. Once an adaptive acceleration curve is initiated using a microcontroller, the data obtained by the infrared sensors are automatically recorded and analyzed in a computer. For comparison purposes, 3 week training is conducted on rats using a treadmill, an MRW and a PRW. After surgically inducing middle cerebral artery occlusion (MCAo), modified neurological severity scores (mNSS) and an inclined plane test were conducted to assess the neurological damages to the rats. PRW is experimentally validated as the most effective among such animal mobility systems. Furthermore, an exercise effectiveness measure, based on rat position analysis, showed that there is a high negative correlation between the effective exercise and the infarct volume, and can be employed to quantify a rat training in any type of brain damage reduction experiments.

Introduction

Strokes exist continuously as a financial burden to countries globally, leaving countless patients physically and mentally disabled1,2. There is clinical evidence to suggest that regular exercise can improve nerve regeneration and strengthen neural connections3,4, and it is also shown that exercise can decrease the risk of suffering ischemic strokes5. With either a treadmill or a running wheel as an exercise training system, rodents, such as rats, serve as a proxy for humans for testing the effectiveness of exercises in a vast majority of clinical experiments6-8. A training system normally involves training a rat for a certain period of time, during which a rat runs at a certain speed. Therefore, the training intensity is generally calculated according to the exercise speed and duration6-8. The same approach is applied to estimate the amount of exercise required for neurophysiological protection. However, the experimental exercises are sometimes found to be ineffective, such as when a rat stumbles, falls, or grabs the rails once they are unable to catch up with the running wheel speed9-11. Needless to say, incidents of ineffective exercise significantly reduce the exercise benefit. Even though there is no any universally accepted approach currently to quantify the effective exercises for reducing brain damage, the level of effective exercises still stands as an objective appraisal for clinical researchers to illustrate the benefits of exercise in the discipline of neurophysiology.

There exist a number of limitations on commercially available animal mobility systems used in today's brain damage reduction experiments12. In a treadmill case, rats are forced to run by means of electric shocks, inducing tremendous psychological stress on the animals and thereby interference in the final neurophysiological test results8,13,14. Running wheels can be categorized into two types, namely voluntary and forced. Voluntary running wheels allow rats to run naturally, creating excessive variability due of the differences in the rats' physical traits and abilities15, while motorized running wheels (MRWs) employ a motor to turn the wheel, forcing rats to run. Despite also being a form of forced training, MRWs imposes less psychological stress on rats than treadmills13,16,17. However, experiments using MRWs have reported that rats sometimes interrupt the exercise by grabbing the rails on the wheel track and refusing to run at speeds exceeding 20 m/min9. These examples show that animal mobility systems currently available have an inherent disadvantage that inhibits effective exercising. For objective rat training purposes, the development of a highly effective training system but with low interference is therefore viewed as an urgent issue for neurophysiological exercise experiments.

This study presents a highly effective running wheel system for experiments on reducing the severity of the effects of the stroke11. In addition to a reduced number of interference factors during a training process, this system detects the running position of a rat using infrared sensors embedded in the wheel, thereby achieving a more reliable estimate of effective exercise activity. The psychological stress imposed by traditional treadmills and the frequent exercise interruptions in MRWs both skew the objectivity of the resulting exercise estimates. A positioning running wheel (PRW) system presented in this study is developed in an attempt to minimize the unwanted interference while providing a reliable training model for quantifying effective exercise.

Protocol

Ethics Statement: The experimental procedures were approved by the animal ethics committee of Southern Taiwan University of Science and Technology Laboratory Animal Center, National Science Council, Republic of China (Tainan, Taiwan).

1. Constructing the Running Wheel Structure

NOTE: All acrylic should be transparent. Wash the disassembled wheel with water, then use alcohol to wipe the rubber track and acrylic sheets after each use.  

  1. Obtain an acrylic running wheel to be 55 cm in diameter and 15 cm in width.
    NOTE: This wheel is larger than a traditional running wheel (diameter = 35 cm; width = 12 cm) (Figure 1A).
  2. Using a cutter, cut a quarter-circle opening into one side of the running wheel to act as an entrance and an exit as well for rats (Figure 1B). Place a layer of high-friction rubber track on the inside of the acrylic wheel (Figure 1B).
  3. Place an iron rod with bearings to connect the running wheel (Figure 1B). Place two acrylic triangular columns on either side of the running wheel to act as the support frame (Figure 1B).
  4. Attach a 1 mm thick semicircular, transparent acrylic sheet to the external sides of the two triangular columns using screws. Use this sheet to deploy the infrared sensors. Ensure that the acrylic sheets are approximately 3 cm away from each side of the running wheel.

2. Deploying the Infrared Sensors and Defining the Effective Exercise Area

NOTE: Take into account the running wheel size and the rat length in the design of an infrared system. A rat only triggers a single sensor at a time. In this experiment, rats are between 20 and 23 cm long.

  1. Drill a hole in the acrylic sheets every 45° (arc interval = 21 cm), with the distance between two holes being roughly equivalent to the length of a test rat. Make the holes the same size as the infrared sensors (Figure 2A).
    NOTE: For traditional MRWs, drill a hole every 70° (arc interval = 21 cm, Figure 2B).
  2. During a PRW experiment, maintain the rats at a steady state of running between 0° to 135°.
    NOTE: Thus define this area as the effective exercise area, while view all the other sections as the ineffective exercise areas. For traditional MRWs, define the effective exercise area as the portion between 0° to 140° (Figure 2B).

3. Driving the Running Wheel

  1. Use a brushless DC motor and a motor driver to drive the running wheel.
  2. Mount a 10 cm diameter rubber disk on the motor’s central axis (Figure 1B).
  3. Using the iron frame and springs to support the motor, connect the rubber disk from the motor’s central axis to the outer side of the running wheel.
    NOTE: The springs must cooperate with the screws to allow dynamic motor height adjustments and to prevent rubber disk from being disconnected to the running wheel track because of loose springs.
  4. Operate the motor to drive the 10 cm diameter rubber disk using a microcontroller, and observe the wheel rotate due to the friction between the rubber disk and the runway of wheel, creating a motorized running wheel platform.
  5. Mount four infrared sensors sequentially between 0° to 135° (Figure 2A).
    NOTE: For traditional MRWs, mount sensors between 0° to 140° (Figure 2B).
  6. Connect four pairs of infrared sensors mounted in both acrylic sheets to the microcontroller’s general pins using single core cables, thereby forming a positioning running wheel system.

4. Constructing an Adaptive Acceleration Curve

  1. Three days before the commencement of official 3 week exercise training, train rats by manually operating the running wheel.
    NOTE: The goal is to allow the rats to become familiar with the running environment, and is to test whether each rat can endure running at 20 m/min.
    1. During the manually operated training, gradually accelerate the running speed until a rat is unable to keep pace. When this occurs, decrease the speed until the rat regains a steady running pace, and then gradually increase the speed again until the rat reaches 20 m/min (dashed lines in Figure 3). The manual training involves seven rats to construct the training curves.
  2. Using a numerical equation to fit the measured data on Day 3 of the manual testing, calculate the acceleration curves closest to the manual training (the curve with circles, Figure 3). Fit Equation 1 to raw data, where Cini = 8, Cfin = 20 and τ = 30 represent the initial velocity, the final velocity and the time constant, respectively).
    NOTE: This equation adapts to a rat’s body condition. Therefore, refer to the calculated curve as an adaptive acceleration-training model.
    figure-protocol-5273  (1)
  3. Use Equation 1 for Week 1 of the formal training.
  4. For Weeks 2 and 3 of the training, adjust the parameters of Equation 1, that is to say, change A from 12 to 22, to allow the speed to reach 30 m/min.

5. Controlling the Software Program

NOTE: Exclusively develop a code for the microcontroller-based motor operation and for signal transmission from the infrared sensors to a computer for subsequent data analysis.

  1. Use C programming language to write a software control program containing one main program and two interrupt-service routines for the timer in the microcontroller18.
    1. Ensure that the main program initializes the microcontroller’s register and constructs an adaptive acceleration curve model in the microcontroller’s memory.
    2. Use the interrupt-service routine of Timer 0 to activate the adaptive acceleration curve and calculate the entire training duration.
    3. Use the interrupt-service routine of Timer 1 to extract the signal data from the infrared sensors and to transfer the data to the computer.
    4. Use the main program to record the position of 0o to adjust the speed of running wheel.
  2. Once the receiving IR sensor at 0° is triggered, interpret it as a fall incidence, which is accumulated by the main program. The moment the occurrence times of fall incidences hits the 10% threshold of the number of the rat position detections, deaccelerate the running wheel automatically as a safety measure for trained rats. NOTE: The speed of running wheel is reduced until the rat can return to the safe zone (0o to 135o) and maintain a stable running state for the safety measure.

6. Operating the Positioning Running Wheel System

  1. Turn on the microcontroller and wait for an operator to press the button to start each week’s training model.
    1. Press the “Start” button to begin the training model for Week 1.
      NOTE: The motor automatically accelerates based on the adaptive acceleration curve until it reaches 20 m/min, and automatically stops after 30 min.
    2. Press the “Start” button to begin the training model for Week 2.
      NOTE: The motor automatically accelerates based on the adaptive acceleration curve until it reaches 30 m/min, and automatically stops after 30 min.
    3. Press the “Start” button to begin the training model for Week 3.
      NOTE: The motor automatically accelerates based on the adaptive acceleration curve until it reaches 30 m/min, and automatically stops after 60 min.
      NOTE: Throughout the entire training process, transmit the signal data received from the infrared sensors to a computer wirelessly.
  2. Using a computer, analyze the location data to obtain an effective exercise measure for the entire exercise process (figure-protocol-8392). See Equation 2.
    figure-protocol-8485  (2)
    NOTE: EEE, EED and IED represent the effective exercise measure, the effective and ineffective exercise durations, respectively.

7. Training the Rats

  1. Randomly divide adult male Sprague-Dawley rats into five groups (n = 9 for each group): the sham, control, treadmill, MRW and PRW groups.
  2. Conduct a 3 week exercise training for the three exercise groups, i.e. the treadmill, MRW and PRW groups, while do not for the sham and the control groups.
    NOTE: The 3 week exercise training for each exercise group is 20 m/min for 30 min during Week 1, 30 m/min for 30 min during Week 2 and 30 m/min for 60 min during Week 3.

8. Animal and Stroke Model

  1. As stated in Sec. 7.1, randomly divide all the involved adult male Sprague-Dawley rats, weighing between 250-280 g, into 5 groups.
  2. Weigh all the animals to ensure accurate drug dosage calculations. Anesthetize the rats with sodium pentobarbital (25 mg/kg, intraperitoneally [i.p.]) and a mixture containing ketamine (4.4 mg/ kg, intramuscularly [i.m.]), atropine (0.02633 mg/kg, [i.m.]) and xylazine (6.77 mg/kg, [i.m.]).
    1. Assess the anesthetic depth by monitoring the breathing rate (normal 70-115 breaths/min), rhythm, depth of respiration, mucous membrane color and regular testing of reflexes, e.g. toe pinch, tail pinch, eyelid/eyelash and palpebral.
  3. Insert temperature probes into the rectum, and maintain the rectal temperatures between 37 to 37.5 °C using separate heating lamps.
  4. Induce focal ischemia, transient middle cerebral artery occlusion (MCAo) by inserting a filament into the internal carotid artery to occlude the orifice of the middle cerebral artery via external carotid artery approach19.
    1. Perform the same operating procedures on the sham-operated animals, while do not insert a filament into the internal carotid artery. Maintain focal cerebral ischemia for 1 hr, remove the filament, close the incision, and then leave 1 cm of the nylon suture protruding, which could be withdrawn to allow reperfusion.
  5. Administer subcutaneous (s.c.) injections of an analgesic (buprenorphine (0.05 mg/kg, s.c.)), into the animals for analgesia twice a day for 3 days.

9. Assessing Neural Damage

  1. Evaluate neurological and motor functions, respectively, by the neurological severity score (mNSS)20 and an inclined plane test21.
    NOTE: mNSS is a composite of the motor (muscle status, abnormal movement), sensory (visual, tactile and proprioceptive) and reflex tests. Give one point for failure to perform a task. Rate neurological function on a scale of 0-18 (normal score = 0; maximal deficit score = 18).
  2. Assess all the rats in terms of behavioral performance the day before and daily over a time span of 7 days after the surgery.
  3. Measure the hind limb grip strength of the rat using an inclined plane.
    1. Place rats on the inclined climbing apparatus on a daily basis, and acclimatize the rats to the apparatus and the testing conditions 1 week before testing.
    2. Place each rat on the apparatus and encourage the rat to climb the platform until the top of the apparatus during the acclimatization period.
    3. Place the rat at the top of the apparatus with the head downward during testing. Ensure that the body axis of the rat stays along to a 20 x 20 cm2 rubber ribbed surface on the inclined plane starting at an angle of 25°.
    4. Increase the angle dynamically using a ball screw connected with a stepper motor to determine the maximal angle at which an animal could hold to the plane. Increase the angle of the inclined plane gradually until the mouse failed to hold on the inclined plane, and then detect a sliding down event. The baseline degree of inclined plane is 25° in the beginning.
    5. Ask two observers (unaware of what treatment the rats had been given), to independently examine and score all the behavioral tests, i.e. the mean of the left- and right-side maximal angles.
  4. Sacrifice all the animals on day 7 after MCAo. Perfuse the hearts of the animals under deep anesthesia (sodium pentobarbital 100 mg/kg, i.p.) with saline22. Remove and then immerse the brain tissue in cold saline for 5 min, which is then sliced into 2.0 mm coronal sections using a tissue slicer22.
  5. Submerge the fresh brain sections into 2, 3, 5-triphenyltetrazolium chloride (TTC) at 37 °C for 30 min, then transfer the slices to 5% formaldehyde solution for fixation at 4 °C for 24 hr. Place the stained brain slices on a plexiglas holder.
  6. Photograph the TTC-stained slices with a calibrated scale using a CCD camera linked to a personal computer loaded with image processing software. Use a semi-automated image analysis system as well to estimate the infarcted area (mm2) from each TTC-stained brain slice23.
  7. Calculate the total infarct volume for each slice by summation of infarcted areas of all brain slices. Mark the unstained area (ischemic brain) separately on each side of 2 mm thick slices, then calculate the infarct volume and the mean value.
  8. Calculate the corrected infarct volume (CIV) as
    CIV= {LT- (RT- RI)} figure-protocol-14071 d (3)
    NOTE: Where LT and RT denote the areas of the left and right hemispheres in mm2, respectively, RI is the infarcted area in mm2, and d = 2 mm is the slice thickness.

Results

This section is devoted to comparisons, made 1 week after surgery, on the mNSS scores, incline plane test results and brain infarct volumes among five groups. Figure 4A and 4B present the average mNSS scores and the average of incline plane test results, respectively. The PRW group appears as the best in terms of mNSS improvement. The significant differences between PRW and MRW and between treadmill and PRW clearly suggest that the PRW protects against st...

Discussion

This protocol describes a highly effective running wheel system for reducing the severity of the effects of the stroke in animals. As a rat-friendly testbed, this platform is designed as well in such a way that a stable running speed can be maintained by rats throughout a running process by means of a predetermined adaptive acceleration curve. In typical training systems, preset training speeds and durations are set manually. Once an exercise commences, a preset speed is reached very shortly. In this context, i...

Disclosures

The authors have nothing to disclose.

Acknowledgements

The authors would like to thank Dr. Jhi-Joung Wang, who is the Vice Superintendent of Education at Chi-Mei Medical Center, and Dr. Chih-Chan Lin from the Laboratory Animal Center, Department of Medical Research, Chi-Mei Medical Center, 901 Zhonghua, Yongkang Dist., Tainan City 701, Taiwan, for providing the shooting venue. They would also like to thank Miss Ling-Yu Tang and Mr. Chung-Ham Wang from the Department of Medical Research, Chi-Mei Medical Center, Tainan, Taiwan, for their valuable assistance in demonstrating the prototype system in real experiments with rats. The author gratefully acknowledges the support provided for this study by the Ministry of Science and Technology (MOST 104- 2218-E-167-001-) of Taiwan.

Materials

NameCompanyCatalog NumberComments
Brushless DC motorOriental MotorBLEM512-GFS
Motor driverOriental MotorBLED12A
Motor reducerOriental MotorGFS5G20
SpeedometerOriental MotorOPX-2A
TreadmillColumbus InstrumentsExer-6M
Infrared transmitter Seeed StudioTSAL6200
Infrared ReceiverSeeed StudioTSOP382
MicrocontrollerSilicon LabsC8051F330
CCD cameraCanon Inc.EOS 450D
Image processing softwareAdobe Systems IncorporatedADOBE Photoshop CS5 12.0
Image analysisMedia CyberneticsPro Plus 4.50.29
Sodium pentobarbitalSigma-Aldrich (Saint Louis, MO, USA)SIGMA P-3761
KetaminePfizer (Kent, UK) 1867-66-9
AtropineTaiwan Biotech Co., Ltd. (Taoyuan, Taiwan)A03BA01
XylazineSigma-Aldrich (Saint Louis, MO, USA)SIGMA X1126
BuprenorphineSigma-Aldrich (Saint Louis, MO, USA)B9275

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