The Effect of Anti-Fatigue Decoction on the Behaviors and Serological Indicators in a Central Fatigue Rat Model

Summary

Here, we introduce a protocol to assess the effects of anti-fatigue decoction (AFD) on central fatigue in rats modeled by the modified multiple platform method (MMPM) by monitoring both their behavioral responses and serological markers.

Abstract

This study aimed to assess the effects of Anti-fatigue Decoction (AFD) against central fatigue by observing the behaviors and serological indicators of rats modeled by the modified multiple platform method (MMPM) after drug intervention. Grip strength measurements were used to evaluate the muscle strength of rats. The open field test was utilized to assess anxiety-like behavior, while the Morris water maze test was conducted to evaluate the memory function of the rats. Following the behavioral assessments, rat serum samples were collected to measure the concentrations of corticosterone (CORT) and lactic acid (LAC). The concentration of LAC was determined using the colorimetric method, while the concentration of CORT was measured using the enzyme-linked immunosorbent assay (ELISA) method. Compared to the blank control group, following MMPM modeling, rats exhibited significant reductions in grip strength and impaired ability to memory. The serum analysis revealed increased levels of LAC and CORT in the model group rats. AFD can noticeably reverse these adverse changes to a certain extent. These findings highlight the positive effects of AFD and coenzymeQ10 on physical and cognitive abilities and alterations in serum biomarker levels of central fatigue rats.

Introduction

Fatigue is a multifaceted and non-specific phenomenon that is typically characterized by feelings of tiredness and reduced ability to function¹. It can be classified as either peripheral fatigue, which occurs at the muscular level, or central fatigue, originating in the central nervous system^3,4. Prolonged central fatigue can be a significant contributor to psychological issues, including anxiety, depression, psychological distress, and memory problems^5,6. Despite causing significant distress, there is a scarcity of specific medications targeting central fatigue⁷. While methylphenidate, a central nervous system stimulant, can provide temporary relief, its side effects, like insomnia and palpitations may worsen the condition^8,9.

In previous clinical applications, traditional Chinese medicine has shown promising results in treating central fatigue, incorporating approaches such as oral decoctions, acupuncture, and Tai Chi^10,11,12. Anti-fatigue decoction (AFD) is an effective formula developed by Professor Li Feng based on extensive clinical experience and has demonstrated positive therapeutic effects. It consists of Astragalus membranaceus (Huangqi), Fructus aurantii (Zhiqiao), Fructus crataegi (Shanzha), Schisandra chinensis (Wuweizi), Angelica sinensis (Danggui), and Dendrobium officinale (Shihu), in a ratio of 15: 15: 10: 5: 7: 8. AFD decoction was concentrated to 110 mL after boiling with ten times the volume of deionized water for 1 h thrice. In a previous study, we established an animal model of central fatigue using the Modified Multiple Platform Method (MMPM) and confirmed the manifestation of central fatigue via behavioral and central nervous system neurotransmitter evaluations¹³. In this study, we utilized the AFD intervention in the animal model of central fatigue to evaluate its pharmacological effects through behavioral assessments.

Protocol

This research work adheres to ethical guidelines for animal welfare. Proper care and housing conditions were maintained to ensure the health and well-being of the animals, and all procedures were approved by the institutional animal care and use committee of the Beijing University of Chinese Medicine (BUCM-4-2019041504-2094).

1. Animal raising and grouping

NOTE: Throughout the study, animal welfare was maintained following the 3Rs (Reduction, Refinement, and Replacement) principles.

1. For this study, select 54 six-week-old specific pathogen-free (SPF) Wistar rats with a body weight of 210 g ± 10 g.
2. House the rats in the animal facility under controlled conditions: temperature of 23 ± 2 °C, relative humidity of 50%, and a 12 h/12 h light/dark cycle. Allow the animals to acclimatize for 3 days before the experiment.
3. Randomly divide the rats into a blank control group (labeled as "a" in the figures), a model group (labeled as "b" in the figures), an AFD-low dose (AFD-L; labeled as "c" in the figures) group, an AFD-medium dose (AFD-M; labeled as "d" in the figures) group, an AFD-high dose (AFD-H; labeled as "e" in the figures) group, a Coenzyme Q10 (CoQ10; labeled as "f" in the figures) group, with 9 rats in each group, using a random number table method.

2. Modeling and intervention

NOTE: The establishment of this model was based on the previous literature¹³.

1. Use the self-made modeling box (provided by the Neuroimmunology Laboratory of the Beijing University of Chinese Medicine).
   NOTE: The modeling box has a length of 110 cm, a width of 60 cm, and a height of 40 cm. The bottom is fixed with 15 circular platforms (diameter 6.5 cm, height 8 cm). The horizontal spacing between the two platforms is 13 cm, and the vertical spacing is 10 cm. The open field box has a length, width, and height of 100 cm, 100 cm, and 35 cm, respectively. The bottom is black, and the wall is dark blue. The bottom of the open field box is divided into 25 square sections with dimensions of 25 cm, with the central 9 squares designated as the central zone and the outer 16 squares as the peripheral zone.
2. Ensure that the water level in the pool is approximately 1 cm above the platform and that the water temperature is maintained at 23 ± 2 °C.
3. After the experiment starts, place the rat in the box covered with wire mesh on the surface and press it down with weights to prevent the animals from escaping. Suspend sufficient food beneath the wire mesh and provide clean drinking water.
4. Place the rat in the model group in the box at 18:00 every day and take it out at 8:00 the next day. After each modeling session, dry the rat and place it back in a clean cage. Perform the modeling continuously for 21 days.
5. During the experiment, clean the box, change the water daily, and provide sufficient food.
6. On the 15^th day of modeling, administer the agents via gastric lavage at 10:00 AM every day for a continuous period of 7 days.
   1. Administer the AFD-L group at a dosage of 3.24 g/kg/d, the AFD-M group at 6.48 g/kg/d, and the AFD-H group at 12.96 g/kg/d. Administer coenzyme Q10 at a dosage of 10 mg/kg/d.
   2. When administering the agents via gastric lavage, prepare a suspension by mixing the required dose in distilled water. The volume of administration for each group is 10 mL/kg. Give the blank and model groups the same amount of distilled water.
      NOTE: The dosages administered to the rats were calculated using the body surface area (BSA) method and converted according to the normal therapeutic dosages for humans¹⁴.

3. Behavioral assessments

1. Grip strength of rats
   1. Grasp the rat's tail and gently place it on the grip strength meter.
   2. Pull the rat backward with a uniform force while ensuring the computer system correctly records the data.
      NOTE: Before experiments, technicians were trained to handle the rats to apply force consistently.
   3. Repeat this process three times and calculate the average of the three measurements as the final grip strength value.
      NOTE: To minimize errors caused by human factors, let one person conduct the entire experiment.
2. Open field test in rats
   1. Conduct the behavior experiments in a dimly lit and quiet environment. Before the start of each experiment, place the rats in the behavior room for 1 h of adaptation.
   2. Ensure three experimenters are involved in the operation and wear black clothing when placing or guiding the rats. Throughout the experiment, ensure that the experimenters do not cross the box's boundaries with their bodies or arms.
   3. Open the analysis software.
      1. Click on File in the top menu, and select New Experiment to create a new project. In the Arena Settings, choose the shape corresponding to the arena where the rat will move.
      2. Using the mouse, draw the arena on the screen. Calibrate the camera and Save the arena settings.
   4. Allow a second experimenter, dressed in black clothing, to hold the rat by its back, sequentially place it in the center of the designated area, and quickly withdraw his hand.
   5. Start a new recording. Set the recording duration to 5 min.
   6. After the 5 min observation period, swiftly remove the rat from the open field box and clean its feces. Use 75% alcohol to clean the open field box.
   7. Repeat the process for all rats.
   8. Observe and record (1) the total distance moved, (2) the number of central zone crossings: number of times the rat's limbs cross into central grid squares, and (3) time spent in the central zone, i.e., time spent by the rat in the 9 central grid squares.
3. Morris water maze in rats
   1. Conduct the behavior experiments in a dimly lit and quiet environment. Before starting each experiment, place the rats in the behavior room for 1 h of adaptation.
      NOTE: The rats underwent 4 training days; on the 5^th day, the formal experiment began.
   2. Ensure that the water level in the pool is approximately 1 cm above the platform and that the water temperature is maintained at 23 ± 2 °C.
   3. Ensure three experimenters are involved in the operation and wear black clothing when placing or guiding the rats.
   4. Divide the water pool into four quadrants. Fix a platform in the middle of the second quadrant. Attach different colored and shaped pieces of paper to the center of each quadrant's walls.
   5. Open the analysis software.
      1. Click on File in the top menu, and select New Experiment to create a new project. In the Arena Settings, choose the shape corresponding to the arena where the rat will move.
      2. Using the mouse, draw the arena on the screen. Calibrate the camera and Save the arena settings.
   6. During the learning period, let another experimenter sequentially place the rat facing the pool wall in each quadrant. The order of placement is different each day as follows:
      1. On the first day, place the rat in the following order: first quadrant, second quadrant, third quadrant, fourth quadrant.
      2. On the second day, place the rat in the following order: second quadrant, first quadrant, fourth quadrant, third quadrant.
      3. On the third day, place the rat in the following order: fourth quadrant, third quadrant, second quadrant, first quadrant;
      4. On the fourth day, place the rat in the following order: third quadrant, first quadrant, fourth quadrant, second quadrant.
   7. If the rat fails to find the platform within 120 s, guide it to the platform and allow it to stay on it for 10 s.
   8. After completing the daily experiment, let the third experimenter wipe off the water from the rat's body using a towel and dry it with a hairdryer. Perform this in another room to avoid noise interference.
   9. In the formal experiment, remove the platform and place the rat in the third quadrant. Record the rat's movement trajectory within 120 s.
   10. Observe and record (1) the time spent in the quadrant where the platform was located, and (2) the escape latency, which is the time it takes for the rat to reach the platform from entering the water pool for the first time.

4. Serum biochemical analysis

1. Sample processing
   NOTE: A fast on food, but not water, was allowed the day before sampling.
   1. Anesthetize the rats using a 2% (w/v) sodium pentobarbital solution via intraperitoneal injection at 0.5 mL/100 g body weight.
   2. After complete anesthesia, collect their blood from the abdominal aorta using a blood sampling vessel.
   3. Place the whole blood at room temperature (RT) for 2 h, then centrifuge it at 4 °C, 1522.38 x g for 20 min to obtain serum. Aliquote and store the serum at -80 °C for further use.
2. Lactic acid (LAC) assay
   NOTE: The concentration of LAC was determined using the colorimetric method.
   1. Mix the enzyme reserve solution and enzyme dilution solution in a 1:100 volume ratio to prepare an enzyme working solution.
   2. Prepare the color developer according to the instructions in the kit.
   3. In a blank tube, add 20 µL of distilled water.
   4. In a standard tube, add 3 mmol/L standard solution.
   5. In a measurement tube, add 20 µL of the sample.
   6. Add 1 mL of enzyme working solution and 0.2 mL of color developer to each tube. Incubate at 37 °C for 10 min and then add 2 mL of the stop solution.
   7. Transfer 200 µL of the reaction solution to a 96-well ELISA plate. Measure the OD value at 530 nm. Calculate the LAC concentration based on the OD values.
      ​NOTE: LAC concentration = (sample well OD value - blank well OD value)/( standard well OD value - blank well OD value) x standard solution concentration x dilution ratio factor.
3. Corticosterone assay
   NOTE: Commercially purchased ELISA kits are used to measure the concentration of cortisone in rat serum.
   1. Prior to the experiment, dilute the antibodies conjugated with horseradish peroxidase (HRP) and washing solution to create a working solution. Add standard samples with concentrations of 0 nmol/L, 5 nmol/L, 15 nmol/L, 30 nmol/L, 60 nmol/L, 120 nmol/L, and 240 nmol/L to the coated plate in 20 µL volumes.
   2. Add the serum samples (20 µL) to the respective wells, followed by the addition of 200 µL of enzyme conjugate. Thoroughly shake the plate and incubate it for 60 min.
   3. Discard the reaction solution, and wash the plate three times with the wash solution (400 µL each time). After drying the plate on absorbent paper, add 100 µL of the substrate color reagent to each well.
   4. Incubate the plate at RT for 15 min, then add 50 µL of the stop solution to each well.
   5. Measure the OD values of each well at 450 nm. Use the OD values of the standard wells to generate a standard curve and then use it to calculate the concentrations of the sample wells.

5. Statistical analysis

1. Perform statistical analysis using an appropriate software application. Represent the measurement data as mean ± standard deviation.
2. If the data followed a normal distribution and showed homogeneity of variances, perform an independent t-test.
3. If the data followed a normal distribution but did not have equality of variances, perform an approximate t-test.
4. If the data did not follow a normal distribution, use non-parametric tests for comparison.
5. Use the Pearson's chi-square test for enumeration/count data analysis.
   NOTE: A significance level of α = 0.05 was chosen, where P < 0.05 is referred to as statistically significant.
6. Generate the figures using an appropriate software application.

Results

Compared to the control group, the rats in the model group exhibited significant decreases in grip strength. However, the administration of AFD at low, medium, and high doses was all able to reverse this effect in a dose-dependent manner, as shown in Figure 1. Similarly, the positive control drug also demonstrated the ability to reverse the grip strength changes (Figure 1).

In the open field test, the model group rats showed reduction...

Discussion

AFD is composed of Astragalus membranaceus (Huangqi), Fructus aurantii (Zhiqiao), Fructus crataegi (Shanzha), Schisandra chinensis (Wuweizi), Angelica sinensis (Danggui), and Dendrobium officinale (Shihu), which is believed to have the function of invigorating the spleen and dispersing the stagnated liver-energy in traditional Chinese medicine. Also, all these herbs are considered to possess a favorable safety profile and are thus commonly used as food in China. In pr...

Materials

Name	Company	Catalog Number	Comments
Corticosterone test kit	German DRG company	EIA4164	Step 4.3
Curve Expert 1.4 software	CurveExpert Professional	Version 1.4	For calculation in corticosterone assay
Ethovision software	Noldus Information Technology , Netherlands	Version 15	analysis software and video tracking system
Grip strength test device	Beijing Zhongshi Di Chuang limited company	ZS-ZL	Step 3.1
Lactic acid test kit	Nanjing Jiancheng Bioengineering Research Institute	A019-2-1	Step 4.2
Modified multiple platform method	Neuroimmunology Laboratory of Beijing University of Chinese Medicine	None	Step 2.1
Morris water maze test device	Beijing Zhongshi Di Chuang limited company	ZS-Morris	Step 3.3
Open field test device	Beijing Zhongshi Di Chuang limited company	ZS-KC	Step 3.2
Prism	GraphPad	Verson 8	For generating figures
SPSS 26.0	IBM	Verson 26.0	Statistical analysis
Wistar rats	SiPeiFu (Beijing) Biotechnology Co., Ltd		license number: SCXK (Jing) 2019-0010