β‑glucan reduces exercise‑induced stress through downregulation of c‑Fos and c‑Jun expression in the brains of exhausted rats

  • Authors:
    • Heeok Hong
    • Chang‑Ju Kim
    • Jae‑Deung Kim
    • Jin‑Hee Seo
  • View Affiliations

  • Published online on: March 4, 2014     https://doi.org/10.3892/mmr.2014.2005
  • Pages: 1660-1666
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Abstract

Immediate‑early genes are involved in acute stress responses in the central nervous system. β‑glucan stimulates innate immune defenses, exerts an anti‑tumor response and increases resistance to a wide variety of types of infection. To date, the effect of β‑glucan on the expression of immediate‑early genes under stressful conditions has not been elucidated. In the present study, the effects of β‑glucan on the expression of the oncogenes c‑Fos and c‑Jun in the hypothalamus, dentate gyrus and dorsal raphe in rats following exhaustive treadmill running were investigated. Male Sprague Dawley rats were randomly divided into five groups (n=10 in each group) as follows: Control, exercise, exercise and 50 mg/kg β‑glucan treatment, exercise and 100 mg/kg β‑glucan treatment, and exercise and 200 mg/kg β‑glucan treatment. Rats in the β‑glucan‑treated groups were administered β‑glucan at the respective dose once per day for seven days. Rats in the exercise groups performed treadmill running once per day for six days. On the seventh day of the experiment, the time to exhaustion in response to treadmill running was determined for the exercise groups. The expression of c‑Fos and c‑Jun in the hypothalamus, dorsal raphe and hippocampus was enhanced by exhaustive treadmill running. Administration of β‑glucan resulted in an increase in the time to exhaustion and the suppression of the exercise‑induced increment in c‑Fos and c‑Jun expression. In conclusion, β‑glucan may exert an alleviating effect on exercise‑induced stress through the suppression of c‑Fos and c‑Jun expression in the brains of exhausted rats.

Introduction

Immediate-early genes are involved in acute stress responses in the central nervous system (1). Stress results in the high expression of immediate-early genes, including c-Fos, c-Jun, JunB and JunD, in the hypothalamic paraventricular nucleus and the central amygdaloid nucleus, suggesting that stress may affect neurotransmitter gene expression through Fos and Jun proteins in these nuclei (2). Stress affects the hypothalamic-pituitary-adrenal axis, resulting in constant secretion of corticosterone from the adrenal gland (3). Immediate-early genes have been considered to be reliable markers for the identification of activated cells under stressful conditions (4,5). Running at moderate or high intensity leads to a significant elevation in the number of c-Fos-positive cells in the paraventricular nucleus (6). c-Fos and c-Jun are known to participate in cell growth, mitosis (7,8), differentiation, development (9,10) and the regulation of the expression of other genes (11,12). Immediate-early genes have an important role in the regulation of the nervous system in response to stress, and the expression of these genes is used as a marker for neuronal activity in the brain following exposure to stressful stimuli (13,14).

Exercise can be employed as a model of the temporary immunosuppression that occurs following severe physical stress, resulting in deterioration of the immune system and leading to infection or cancer (15,16). Prolonged exhaustive exercise leads to central fatigue and this type of fatigue limits endurance exercise performance through limitation of brain function (17,18). As a result, exhaustive treadmill running has been used as an animal model of stressful conditions, and alleviation of brain stress has been shown to result in an increase in the time to exhaustion in response to treadmill running (19,20).

β-glucan is the major structural component of the cell wall in yeast and fungi, including mushrooms. β-glucan prevents oxidative injury, stimulates innate immune defenses, exerts anti-tumor responses and increases resistance to a wide variety of infections (2123). β-glucan also exhibits hypocholesterolemic and anti-coagulant properties, making it a promising candidate for a pharmacological promoter of health (21). Orally administered water-soluble glucan is translocated from the gastrointestinal tract into the systemic circulation and induces protection against infection (22).

Numerous pharmacological effects of β-glucan have been reported; however, the effects of β-glucan on the expression of immediate-early genes under stressful conditions have yet to be elucidated. In the present study, the effects of β-glucan on the expression of c-Fos and c-Jun in the hypothalamus, dentate gyrus and dorsal raphe following exhaustive treadmill running were assessed.

Materials and methods

Animals

Adult male Sprague Dawley rats, weighing 203.7±12.8 g (seven weeks old) were obtained from a commercial breeder (Dae Han Bio Link Co., Chungbuk, Korea). The animals were housed at a controlled temperature (20±2°C) with a 12-h light/dark cycle (light from 7.00 a.m. to 7.00 p.m.). Food and water were available ad libitum. All experimental procedures were performed in accordance with the Animal Care Guidelines of the National Institutes of Health and the Korean Academy of Medical Sciences (Seoul, Korea).

Animals were randomly divided into five groups: Control, exercise, exercise and 50 mg/kg β-glucan treatment, exercise and 100 mg/kg β-glucan treatment, and exercise and 200 mg/kg β-glucan treatment (n=10 in each group). The water-soluble glucan (Tokyo Chemical Industry Co., Ltd., Tokyo, Japan) used in this study was β-1,3-glucan in microparticulate form. The β-glucan solution was diluted with drinking water to concentrations of 50, 100 and 200 mg/kg and was made fresh daily. Rats in the β-glucan treatment groups were administered β-glucan at three different doses (50, 100 and 200 mg/kg of body weight, respectively) per day for seven days. The treatment was administered 60 min prior to the start of exercise, which was conducted as described below. Rats in the control and exercise groups received water by oral gavage once per day for seven days.

Exercise protocols

The physical exercise load applied in the present study consisted of running on a motor-driven treadmill without inclination. Rats in the exercise groups were forced to run on a treadmill for 30 min once per day during a period of six consecutive days, whereas rats in the control group were left on the treadmill without running for 30 min. The exercise load consisted of forced running at a speed of 10 m/min for 10 min, followed by 16 m/min for 10 min and then 21 m/min for a final 10 min.

On the seventh day of the experiment, the time to exhaustion during treadmill running was determined for the exercise groups. The time to exhaustion was defined as the time between the commencement of exercise and the first occurrence of a failure to keep up with the treadmill for a period of ≥3 min. The speeds used for the determination of the time to exhaustion were 10 m/min for 5 min, followed by 16, 18, 21, 24, 26, 29, 32, 34 and 37 m/min for 3 min each and then 40 m/min until exhaustion, as described in a previous study (19).

Brain preparation

The animals were sacrificed on the seventh day of the experiments immediately following determination of the exhaustion time. For preparation of the brains, the animals were fully anesthetized with Zoletil 50® (10 mg/kg, intraperitoneal; Vibac, Carros, France). The rats then received a transcardial perfusion with 50 mM phosphate-buffered saline (PBS) and were fixed with a freshly prepared solution of 4% paraformaldehyde in 100 mM phosphate buffer (pH 7.4). The brains were then removed, post-fixed in the same fixative overnight and transferred to a 30% sucrose solution for cryoprotection. Coronal sections with a thickness of 40 μm were prepared using a frozen microtome (Leica, Nussloch, Germany).

Immunohistochemical detection of c-Jun and c-Fos

Immunohistochemistry was performed for evaluation of c-Fos- and c-Jun-positive cells in the dorsal raphe (bregma, from −7.08 to −7.56 mm), the hypothalamus (bregma, from −1.80 to −1.92 mm) and the hippocampus (bregma, from −2.92 to −3.24 mm), according to the previously described method (14,24). The sections were incubated in PBS for 10 min and then washed three times in the same buffer. The sections were subsequently incubated in 1% hydrogen peroxide (H2O2) for 30 min, prior to being incubated overnight with rabbit anti-c-Fos antibody (1:1,000; Santa Cruz Biotechnology, Inc., Santa Cruz, CA, USA) and rabbit anti-c-Jun antibody (1:1,000; Santa Cruz Biotechnology, Inc.). The sections were then incubated for 1 h with biotinylated anti-rabbit secondary antibody (1:200; Vector Laboratories, Inc., Burlingame, CA, USA) for c-Fos and c-Jun immunohistochemistry. The sections were subsequently incubated with avidin-biotin-peroxidase complex (1:100; Vector Laboratories, Inc.) for 1 h at room temperature. For staining, the sections were incubated in a solution consisting of 0.05% 3,3′-diaminobenzidine tetrahydrochloride and 0.03% H2O2 in 50 mM Tris-HCl (pH 7.6) for ~5 min, washed with PBS and mounted onto gelatin-coated slides. The slides were air-dried overnight at room temperature and coverslips were mounted using Permount mounting medium (Thermo Fisher Scientific, Inc., Waltham, MA, USA). The numbers of c-Fos- and c-Jun-positive cells in the dorsal raphe, the hypothalamus and hippocampus were counted hemilaterally using a microscope (Olympus, Tokyo, Japan).

Statistical analysis

Values are expressed as the mean ± standard error of the mean. Data were analyzed by one-way analysis of variance, followed by Duncan’s post hoc test using SPSS software (SPSS, Inc., Chicago, IL, USA). P<0.05 was considered to indicate a statistically significant difference.

Results

Effect of β-glucan on time to exhaustion during treadmill running

The effects of β-glucan on time to exhaustion are shown in Fig. 1. The average running time until fatigue was 69.88±5.16 min in the exercise, 81.66±2.34 min in the 50 mg/kg β-glucan-treated, 88.66±5.42 min in the 100 mg/kg β-glucan-treated and 91.77±4.04 min in the 200 mg/kg β-glucan-treated groups. These findings indicate that the time to exhaustion in response to treadmill running increased following treatment with β-glucan (P<0.05). In particular, treatment with 100 and 200 mg/kg β-glucan resulted in a significant increase in the time to exhaustion by treadmill running as compared with the exercise group (P<0.05).

Effect of β-glucan on the expression of c-Fos in the hypothalamus, dentate gyrus and dorsal raphe

Photomicrographs of c-Fos-positive cells in the hypothalamus, dentate gyrus and dorsal raphe are shown in Fig. 2. The number of c-Fos-positive cells in the hypothalamus was 19.28±1.78 in the control, 190.71±30.56 in the exercise, 175.42±19.98 in the 50 mg/kg β-glucan-treated, 98.14±18.54 in the 100 mg/kg β-glucan-treated and 133.57±10.35 in the 200 mg/kg β-glucan-treated groups. These results demonstrate that treadmill exercise led to increased expression of c-Fos in the hypothalamus (P<0.05) and that treatment with β-glucan resulted in the suppression of the exercise-induced expression of c-Fos (P<0.05). In particular, treatment with β-glucan at 100 mg/kg resulted in the statistically significant suppression of c-Fos expression in the hypothalamus as compared with the exercise group (P<0.05) (Fig. 3).

The number of c-Fos-positive cells in the dentate gyrus was 57.50±3.43 in the control, 1,218.66±65.97 in the exercise, 888.66±56.14 in the 50 mg/kg β-glucan-treated, 614.66±37.38 in the 100 mg/kg β-glucan-treated and 688.83±73.88 in the 200 mg/kg β-glucan-treated groups. These results demonstrate that treadmill exercise led to increased expression of c-Fos in the dentate gyrus (P<0.05) and that treatment with β-glucan resulted in the suppression of the exercise-induced expression of c-Fos (P<0.05). In particular, treatment with β-glucan at 100 and 200 mg/kg resulted in the statistically significant suppression of c-Fos expression in the dentate gyrus as compared with the exercise group (P<0.05) (Fig. 3).

The number of c-Fos-positive cells in the dorsal raphe was 180.42±13.19 in the control, 705.00±19.11 in the exercise, 623.00±19.71 in the 50 mg/kg β-glucan-treated, 476.57±20.41 in the 100 mg/kg β-glucan-treated and 475.00±40.13 in the 200 mg/kg β-glucan-treated groups. These results demonstrate that treadmill exercise led to increased expression of c-Fos in the dorsal raphe (P<0.05) and that treatment with β-glucan resulted in the suppression of the exercise-induced expression of c-Fos (P<0.05). In particular, treatment with β-glucan at 100 and 200 mg/kg resulted in the statistically significant suppression of c-Fos expression in the dorsal raphe as compared with the exercise group (P<0.05) (Fig. 3).

Effect of β-glucan on expression of c-Jun in the hypothalamus, dentate gyrus and dorsal raphe

Photomicrographs of c-Jun-positive cells in the hypothalamus, dentate gyrus and dorsal raphe are shown in Fig. 4. The number of c-Jun-positive cells in the hypothalamus was 26.88±2.45 in the control, 130.88±17.85 in the exercise, 117.22±13.73 in the 50 mg/kg β-glucan-treated, 70.55±10.34 in the 100 mg/kg β-glucan-treated and 97.22±5.65 in the 200 mg/kg β-glucan-treated groups. These results demonstrate that treadmill exercise led to increased expression of c-Jun in the hypothalamus (P<0.05) and that treatment with β-glucan resulted in the suppression of the exercise-induced expression of c-Jun (P<0.05). In particular, treatment with β-glucan at 100 mg/kg resulted in the statistically significant suppression of c-Jun expression in the hypothalamus as compared with the exercise group (P<0.05) (Fig. 5).

The number of c-Jun-positive cells in the dentate gyrus was 88.00±2.20 in the control, 122.40±4.61 in the exercise, 103.05±0.65 in the 50 mg/kg β-glucan-treated, 97.83±1.02 in the 100 mg/kg β-glucan-treated and 99.59±1.08 in the 200 mg/kg β-glucan-treated groups. These results demonstrate that treadmill exercise led to increased expression of c-Jun in the dentate gyrus (P<0.05) and that treatment with β-glucan resulted in the suppression of the exercise-induced expression of c-Jun (P<0.05). In particular, treatment with β-glucan resulted in the statistically significant suppression of c-Jun expression in the dentate gyrus as compared with the exercise group (P<0.05) (Fig. 5).

The number of c-Jun-positive cells in the dorsal raphe was 401.33±43.19 in the control, 763.50±51.96 in the exercise, 511.50±31.78 in the 50 mg/kg β-glucan-treated, 468.16±43.82 in the 100 mg/kg β-glucan-treated and 472.16±13.77 in the 200 mg/kg β-glucan-treated groups. These results demonstrate that treadmill exercise led to increased expression of c-Jun in the dorsal raphe (P<0.05) and that treatment with β-glucan resulted in the suppression of the exercise-induced expression of c-Jun (P<0.05). In particular, treatment with β-glucan resulted in statistically significant suppression of c-Jun expression in the dorsal raphe as compared with the exercise group (P<0.05) (Fig. 5).

Discussion

Previous studies have used the expression of c-Fos and c-Jun as a marker for stimuli-induced changes in the metabolic activity of neurons under various conditions (1,2,25,26). The application of stressful stimuli resulted in the enhanced expression of c-Fos and c-Jun (6,14,24,27). The expression of four immediate-early genes (c-Fos, c-Jun, JunB and NGFI-B) was increased following 30 min of global ischemia (24). Rats receiving predator stress during pregnancy exhibited anxiety-like behavior with higher expression of c-Fos in the hypothalamus and locus coeruleus following delivery (14). Running at a moderate speed (25 m/min) led to increased induction of c-Fos in various hypothalamic regions; however, running at a low speed (15 m/min) had no effect on the expression of c-Fos (6). Expression of c-Fos in the brain areas associated with micturition was enhanced by the induction of stress urinary incontinence and the suppression of c-Fos expression led to amelioration of the symptoms of stress urinary incontinence (27). These results suggest that neuronal activation in the micturition centers was induced by stress urinary incontinence. The performance of acute exercise led to upregulated expression of c-Fos and c-Jun through activation of the mitogen-activated protein kinase signaling pathway (28). According to the present study, expression of c-Fos and c-Jun in the hypothalamus, dentate gyrus and dorsal raphe was enhanced by exhaustive treadmill running (Figs. 3 and 5), indicating that strenuous exercise acted as a form of physical stress and resulted in the enhancement of c-Fos and c-Jun expression in the brain.

Pharmacological agents acting as ergogenic aids through a reduction in fatigue have been widely investigated (1719). Caffeine and Paeonia radix exhibited ergogenic effects during exhaustive treadmill running (17,18). Seo et al (19) reported that Phellinus linteus enhanced the time to exhaustion in response to treadmill running. Phellinus linteus has been used for the treatment of gastroenteric disorders, inflammation and lymphatic diseases (2931). β-glucan also originates from Phellinus linteus, and the immunological response to β-glucans isolated from medicinal mushrooms has been well documented (32). Prolonged and high-intensity exercise in endurance athletes leads to a deterioration in immune function and increased risk of upper respiratory tract infections. The positive immunomodulatory effect of β-glucan on immunocompetent cells has been reported (33). Treatment with β-glucan increased production of interleukin-2, -4 and -5 and interferon-γ in blood leucocytes, suggesting that β-glucan may alter immune function following strenuous exercise (34). β-glucan from dietary oats reduced the body weight and increased the maximum running time compared with that in control rats (35). In addition, β-glucan from dietary oats decreased the levels of blood urea nitrogen, lactic acid and creatine kinase activity in the serum and increased the levels of non-esterified fatty acids and lactic dehydrogenase activity in the serum as well as the content of liver glycogen. These results suggest that β-glucan from dietary oats can enhance the endurance capacity through the facilitation of recovery from fatigue (35). In the present study, treatment with β-glucan resulted in enhanced time to exhaustion in treadmill running (Fig. 1). Treatment with β-glucan also led to the alleviation of the exercise-induced increase in c-Fos and c-Jun expression in the hypothalamus, dentate gyrus and dorsal raphe (Figs. 3 and 5). These results suggest that β-glucan acted as an ergogenic aid during strenuous exercise through the suppression of stress-related neuronal parameters, including c-Fos and c-Jun, in the brain.

In conclusion, exposure to stressful stimuli, such as strenuous exercise, results in the enhanced expression of c-Fos and c-Jun in the brain. β-glucan reduces exercise-induced stress through downregulation of c-Fos and c-Jun following exhaustive exercise.

Acknowledgements

The present study was supported by the National Research Foundation of Korea Grant funded by the Korean Government (no. NRF-2009-351-G00080).

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Hong H, Kim CJ, Kim JD and Seo JH: β‑glucan reduces exercise‑induced stress through downregulation of c‑Fos and c‑Jun expression in the brains of exhausted rats. Mol Med Rep 9: 1660-1666, 2014
APA
Hong, H., Kim, C., Kim, J., & Seo, J. (2014). β‑glucan reduces exercise‑induced stress through downregulation of c‑Fos and c‑Jun expression in the brains of exhausted rats. Molecular Medicine Reports, 9, 1660-1666. https://doi.org/10.3892/mmr.2014.2005
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Hong, H., Kim, C., Kim, J., Seo, J."β‑glucan reduces exercise‑induced stress through downregulation of c‑Fos and c‑Jun expression in the brains of exhausted rats". Molecular Medicine Reports 9.5 (2014): 1660-1666.
Chicago
Hong, H., Kim, C., Kim, J., Seo, J."β‑glucan reduces exercise‑induced stress through downregulation of c‑Fos and c‑Jun expression in the brains of exhausted rats". Molecular Medicine Reports 9, no. 5 (2014): 1660-1666. https://doi.org/10.3892/mmr.2014.2005