Effect of oat bran on time to exhaustion, glycogen content and serum cytokine profile following exhaustive exercise
© Donatto et al; licensee BioMed Central Ltd. 2010
Received: 19 July 2010
Accepted: 18 October 2010
Published: 18 October 2010
The aim of this study was to evaluate the effect of oat bran supplementation on time to exhaustion, glycogen stores and cytokines in rats submitted to training. The animals were divided into 3 groups: sedentary control group (C), an exercise group that received a control chow (EX) and an exercise group that received a chow supplemented with oat bran (EX-O). Exercised groups were submitted to an eight weeks swimming training protocol. In the last training session, the animals performed exercise to exhaustion, (e.g. incapable to continue the exercise). After the euthanasia of the animals, blood, muscle and hepatic tissue were collected. Plasma cytokines and corticosterone were evaluated. Glycogen concentrations was measured in the soleus and gastrocnemius muscles, and liver. Glycogen synthetase-α gene expression was evaluated in the soleus muscle. Statistical analysis was performed using a factorial ANOVA. Time to exhaustion of the EX-O group was 20% higher (515 ± 3 minutes) when compared with EX group (425 ± 3 minutes) (p = 0.034). For hepatic glycogen, the EX-O group had a 67% higher concentrations when compared with EX (p = 0.022). In the soleus muscle, EX-O group presented a 59.4% higher glycogen concentrations when compared with EX group (p = 0.021). TNF-α was decreased, IL-6, IL-10 and corticosterone increased after exercise, and EX-O presented lower levels of IL-6, IL-10 and corticosterone levels in comparison with EX group. It was concluded that the chow rich in oat bran increase muscle and hepatic glycogen concentrations. The higher glycogen storage may improve endurance performance during training and competitions, and a lower post-exercise inflammatory response can accelerate recovery.
The importance of dietary carbohydrates (CHO) in sporting performance was shown in the classical gaseous exchange experiments and biopsy studies, in which increasing exercise intensity utilises a greater proportion of CHO [1, 2]. These data provided a major breakthrough for the science of sports nutrition, as it enabled the exact amount of CHO for athletes to be quantified.
The recommendations concerning carbohydrates (CHO) for athletes are around 6 g-10 g/Kg/day [3–5] and these quantities vary in accordance with the quantity of body mass, gender, volume and intensity of the training. According to Tarnopolsky  elite athletes train around 8 to 40 hours per week, exponentially increasing their nutritional needs. The International Olympic Committee (IOC) recommends that: "following a diet rich in carbohydrates days before a competition can help to increase sporting performance, particularly when the exercise is kept up for longer than 60 minutes" .
Exhaustive endurance exercise can induce immune disturbances and consequently increase susceptibility to upper respiratory tract infections . Several mechanisms have been proposed in an attempt to explain the susceptibility of athletes to respiratory infections. Cortisol contributes only minimally to the exercise induced rise in liver glucose output , while it plays a role in immune disturbances [9, 10]. Several components of the innate immune system are compromised during single or repeated sessions of exercise stress.
Physical exercise can affect the levels of systemic cytokines, such as TNF-α [11–13], interleukin 1 beta (IL-1β) , IL-6 [12–16], interferon and others . Recently, it has been suggested that the disruptions in the balance between pro- and antiinflammatory cytokines may lead to a loss of inflammatory control, with possible implications for overall immune system function [17, 18]. The effect of ingesting carbohydrates during long duration exercises, with the purpose of attenuating immune suppression is well established [6, 12–14].
Cereals oat bran has a high nutritional quality, an naturally source of CHO , rich in proteins, unsaturated fatty acids, vitamins, and complex starches that comprise the part with the largest quantity of soluble fiber. Another important nutrient in oat bran is β-Glucan, and has well-documented stimulation effects on the immune system. Also may help enhance immune resistance to various viral, bacterial, protozoan, and fungal diseases . Animal studies show that oat β-glucan can offset exercise-induced immune suppression and decrease susceptibility to infection during heavy training . Therefore, the aim of this study was to evaluate the effect of oat bran supplementation on time to exhaustion, glycogen stores and cytokines profile in rats submitted to training.
Materials and methods
All experiments were conducted according to the policy of the American College of Sports Medicine on Research with Experimental Animals. Two-month-old male Wistar rats (Rattus novergicus var. albinus, Rodentia, Mammalia) with a mean ± SEM weight of 200 ± 5 g were used. The animals had free access to water and were fed a commercial chow for rodents (NUVILAB, Purina®) ad libitum. The animals were kept in collective cages (3 rats per cage) at a constant temperature of 23 ± 2°C, and a cycle of 12 hours light/12 hours darkness, with light from 06:00 h to 18:00 h (in pathogen-free housing). Before the experimental period began, the animals underwent 48 hours of adaptation to the research laboratory conditions. The 27 animals were divided into 3 groups (n = 9 each group): sedentary control group that underwent no physical training (C), an exhaustion group that received a control chow (EX) and an exhaustion group that received a chow supplemented with 30% of soluble oat bran fibers (EX-O). All experiments conducted on animals were previously approved by the Ethics Committee on Animal Testing, Federal University of San Carlos.
Nutritional Composition in grams (g) of the chows used.
Total fibers (g)
Insoluble fibers (g)
Soluble fibers (g)
The animals were submitted to a 5-day period of adaptation to the liquid environment (5 minutes on the first day, 15 minutes on the second, 30 minutes on the third, 45 minutes on the fourth and 60 minutes on the fifth), in accordance with Sampaio-Barros . Importantly, the control groups were submitted in contact with water, but did not perform the exercise. This was done to equalize the stress compared to the exercised group. A tank was used to perform the swimming sessions, were made of plastic and did not have places where animals could cling to. This was necessary to achieve constant exercise. The water temperature was monitored at approximately 28 ± 2°C. After adaptation, the training consisted of 60 minutes of daily swimming, five days per week, for eight weeks, performed in the afternoon between 14:00-17:00. The moderate intensity they used a load of 5% of their body weight strapped to their backs, which corresponds to intensity below the point of inflection of the lactate threshold curve. At the end of eight weeks training, the animals were submitted to the exhaustion test, characterized by being incapable of keeping themselves on the surface of the water [24, 25].
Animal sacrifice and sample collection
Immediately after the exhaustion test, the animals were sacrificed by decapitation. During exsanguination, the mixed arteriovenous blood was collected in heparinized tube and chilled on ice. Blood was then spun at 500g for 15 min to obtain plasma for cytokine and corticosterone analyses. In the following order, the liver, soleus and white and red gastrocnemius muscle were collected and stored at -70°C until the time of measurement of hepatic and muscle glycogen. The white and red portion of the gastrocnemius was divided throughout the major colour of muscle fibres.
Determination of muscle and hepatic glycogen concentrations
The muscle samples were digested in 30% KOH at 100° C and glycogen was precipitated by passage through ethanol. Between each precipitation the sample was centrifuged at 3000 rpm for 15 minutes. The precipitated glycogen was submitted to acid hydrolysis in the presence of phenol. The values were expressed in mg/100 mg of wet weight, using the Siu method .
Determination of serum cytokines
After the period of supplementation and training, measurements of IL-6, TNF-α and IL-10 in plasma were made by ELISA using the R & D Systems Quantikine High Sensitivity kit (R&D Systems, Minneapolis, MN, USA) for each cytokine. The intra-assay coefficient of variance (CV) was 4.1 - 10%, the inter-assay CV was 6.6 - 8%, and the sensitivity was 0.0083 pg/ml . The duplicate plasma aliquots for all cytokines analysis were used.
Plasma corticosterone was determined by ELISA, using the Stressgen kit (Corticosterone ELISA KIT Stressgen@), Michigan, USA). The sensitivity range of the assay was 32-20.000 ng/ml. The duplicate plasma aliquots for hormone analysis were used.
Determination of glycogen synthetase-alpha (GS-α) mRNA expression in the soleus muscle
Total RNA extraction
Total RNA was obtained from 100 mg of soleus muscle. The tissue were stored at -70°C until the time of measurement. Cells were lysed using 1 mL of Trizol reagent (Life Technologies, Rockville, MD, USA). After incubation of 5 min at room temperature, 200 μL chloroform was added to the tubes and centrifuged at 12,000 × g. The aqueous phase was transferred to another tube and the RNA was pelleted by centrifugation (12,000 × g) with cold ethanol and air-dried. After this, RNA pellets were diluted in RNase-free water and treated with DNase I. RNAs were stored at -70°C until the time of measurement. RNA was quantified by measuring absorbance at 260 nm. The purity of the RNAs was assessed by the 260/280 nm ratios and on a 1% agarose gel stained with ethidium bromide at 5 μg per mL .
RT-PCR was performed using parameters described by Innis and Gelfand . The number of cycles used was selected to allow quantitative comparison of the samples in a linear manner. For semi-quantitative PCR analysis, the housekeeping β-actin gene was used as reference. The primer sequences and their respective PCR fragment lengths are: GSK3-α sense: AATCTCGGACACCACCTGAGG - 3'; anti-sense: 5'GGAGGGATGAGAATGGCTTG - 3'. Control: β-actina sense: 5'-ATGAAGATCCTGACCGA GCGTG-3'; anti-sense: 5'- TTGCTGATCCACATCTGCTGG-3'. Published guidelines were followed to guard against bacterial and nucleic acid contamination .
Analysis of the PCR products
The PCR amplification products were analyzed in 1.5% gels containing 0.5 μg per mL of ethidium bromide and were electrophoresed for 1 h at 100 V. The gels were photographed using a DC120 Zoom Digital Camera System from Kodak (Life Technologies, Inc., Rockville, MD, USA). The images were processed and analyzed in the software Kodak Digital Science 1D Image Analysis (Life Technologies). PCR band intensities were expressed as Optic Density (OD) normalized for β-actin expression. Data are presented as a ratio compared with the respective controls, which received an arbitrary value of 1 in each experiment.
Data are presented as mean ± SEM (standard error of the mean). The normality of distribution of all parameters was checked with the Kolmogorov-Smirnov test and by the homocedasticity test (Bartlett criterion). All variables presented normal distribution and homocedasticity, thus the two-way ANOVA test was used, (taking into consideration the variables exercise × oat bran enriched diet) and when the difference presented was significant, Tukey's post hoc test was used. A significance level of p ≤0.05 was used for all comparisons. The software package used was SPSS for Windows version 10.0.
Time to Exhaustion
Corticosterone and Cytokine Concentrations
Plasma cytokine concentration in experimental groups.
11.2 ± 17
163 ± 2.7*
127 ± 3.6*#
50.5 ± 9.4
328.5 ± 78*
84.3 ± 53.4*#
31.1 ± 1.34
5.58 ± 1.0*
2.6 ± 0.4*
Glycogen Concentrations and expression of Glycogen synthetase mRNA
Hepatic and muscle glycogen concentration (mg/100 mg)
5.5 ± 1.06
0.8 ± 0.09*
2.9 ± 0.64*#
0.61 ± 0.06
0.12 ± 0.01*
0.14 ± 0.03*
0.53 ± 0.05
0.14 ± 0.02*
0.16 ± 0.04*
0.70 ± 0.05
0.15 ± 0.06*
0,37 ± 0.04*#
The quantity of glycogen in the white gastrocnemius muscle decreased by 77% in the EX-O (p = 0.011), and 80% in the EX group (p = 0.037) when compared with the control. There were no significant differences between EX-O and EX in the glycogen concentrations of the white gastrocnemius muscle (Table 3).
The exhaustion test diminished the muscle glycogen concentrations of the red gastrocnemius by 69.8% in the EX-O group, and by 73.5% in the EX group (p < 0.05), when compared with the control group. In the comparison between the exercise groups, no significant differences were observed (Table 3).
The aim of this study was to evaluate the effect of oat bran supplementation on time to exhaustion, glycogen stores and cytokines profile in rats submitted to training. The animals did not receive any type of carbohydrate during the time they were performing the exercise, only ad libitum food during the eight weeks of training. In the present investigation, the exercise protocol used was one hour of daily swimming, 5 days per week during two months At the end of the eight weeks, were performed the test exhaust. For the impact in performance, the carbohydrate content should be equal, there by the experimental chows had the same quantity of carbohydrates, being 45.5 g/100 g for the control and 45.6 g/100 g in the experimental chow.
Similarly, in the chows of the present study, one can note a lower quantity of total fibres in the experimental chow (18.9 g) and a higher quantity in the soluble portion (4.5 g). Although the total fibre content was higher (21.9 g) in the control diet, the quantity in the soluble part was lower (3.9 g).The difference in available carbohydrate (avCHO = total carbohydrate minus fiber) is the better explanation: control chow has 45.5 cho-21.9 fiber = 23.6 g avCHO while the oat bran diet contains 45.6 cho-18.9 fiber = 26.7 g avCHO. It is a 13% increase in the oat bran chow.
Changes in the intestinal microflora that occur with the consumption of prebiotic fibres may potentially mediate immune changes via: the direct contact of lactic acid bacteria or bacterial products (cell wall or cytoplasmic components) with immune cells in the intestine; the production of short-chain fatty acids from fibre fermentation; or by changes in mucin production. The link between oat bran and immune system its regard with the content of β-glucan, especially water-soluble β-glucan. This soluble fiber can enhance the activities of both the innate and specific immune system components via direct activation of specific receptors on macrophage, neutrophils, and NK cells [30, 31] or indirectly after activation of pinocytic M-cells located in the Peyer's patches of the small intestine [32, 33]. There is increasing evidence that fermentable dietary fibres and the newly described prebiotics can modulate various properties of the immune system, including those of the gut-associated lymphoid tissues (GALT).
In published data on the immune system of the same experimental group, Donatto  demonstrated that the EX-O group presented better phagocytic capacity of peritoneal macrophages, increased amount of lymphocytes from lymph nodes and shows less leukocytosis after exhausting exercise. We found no side effects in this study, including no increase in the plasma concentration of pro inflammatory cytokine. β-glucan found in oat bran could not exaggerate the inflammatory response to severe exercise.
Glycogen metabolism is largely controlled by the actions of glycogen synthase and glycogen phosphorylase enzymes . The gene expression of Glycogen synthase increased after both resistance and aerobic training, but not when aerobic exercise was combined with a high CHO diet in comparison with diet without exercise . In the present study, we found a lower expression of the glycogen synthetase enzyme in the soleus muscle in the EXO group. Probably, the higher glycogen levels in the soleus muscle had an important relationship with the impaired glycogen synthetase expression. It may reflect a lower need for re-synthesis  since this group presented higher glycogen concentrations in the soleus when compared with exhaustion of the non-oat bran enriched diet group (EX).
The oat bran is a nutritional search of dietary fiber, especially soluble fiber and this nutriente may retard the absorption of nutrients by the intestinal villosities . In this case, the glucose absorption metabolism had a modulation to lower and constant delivery to blood circulation and this could be responsible for a more efficient replacement of muscular glycogen during a longer recovery period [37, 39, 40]. There was a correlation between the low levels of glycogen and higer corticosterone and IL-6. During prolonged and exhausting physical exercises (duration in excess of 90 minutes), the IL-6 has a close relationship with the amount of muscle glycogen and regulation of the homeostasis of blood glucose during long duration exercises. Muscular glycogen and blood glucose are the major sources of substrates for oxidative metabolism, and the immune depletion and fatigue coincides with their depletion, due to the low availability to the skeletal muscle and the central nervous system [41–45].
In the EX group glycogen levels were low while IL-6 and corticosterone were high. In contrast, the inverse was observed in the EX-O group which had higher levels of muscle glycogen and lower levels of corticosterone and IL-6. These results were shown in EX group, since the animals swam an average of 11 hours, ending in a worst metabolic condition On the other hand, EX-O swam an average of 2 hours longer, totalling 13 hours of physical exercise with lower levels of IL-6 and corticosterone, consequently at the end of exercise protocol shows an better condition.
Plasma concentration shows the total secreted of some products like corticosterone and cytokines by all tissues, but does not know the source of secretion. Unfortunately, some of the shortcomings of this study were not to analyze the cytokines levels in different tissues. One of the hypotheses regarding the mechanism of central fatigue is that IL-6 can exert direct influence on hypothalamus-pituitary-adrenal axis, thereby increasing ACTH-cortisol release [15, 46]. Moreover, the different kits used to measure IL-6 plasma levels difficult the comparison between studies.
The exercise protocol used in the present study modulated the serum levels of TNF-α, as a result of the lower levels of TNF-α in the trained groups when compared with the control group. In 1999, Ostrowski and colleagues  presented the plasma cytokines profile after a marathon race (mean duration 3: 26 (h: mi.), with increased levels of TNF-a, IL-6 and IL-10. Their study revealed a proinflammatory and anti-inflammatory profile after a marathon race. Pedersen  suggested that regular exercise modulates some pro-and anti-inflammatory cytokines, induces suppression of TNF-alpha and thereby offers protection against exacerbated inflammation.
Unfortunately, the levels of cytokines in the adipose tissue and muscle were not measured, so that the source of cytokine production cannot be determined. This is an important issue because there is a different production of cytokines in muscle and adipose tissue, and exercise has an influence in this process. Rosa Neto et al.  showed an anti-inflammatory effect of strenuous exercise on muscle and a pro-inflammatory effect on adipose tissue.
In this sense, Pedersen (16) revealed an anti-inflammatory effect of acute physical exercise, characterized by an increased circulating level of IL-10, IL-1 receptor antagonist (IL-1ra) and soluble receptor of TNF (TNFRs). Lira et al.  showed an anti-inflammatory profile on adipose tissue in rats submitted to aerobic training (decreased TNF-alpha and increased IL-10 levels). In the present study, the combination of exercise with oat bran induced a decrease on TNF-alpha levels associated with an increase in IL-10 serum levels (anti-inflammatory cytokine).
These results show that oat bran, how another search of carbohydrate can directly influence the metabolic stress induced by exhaustive long duration exercise, saving the energy reserves and promoting better performance during exercise, thus corroborating findings in the literature [7, 15, 42, 44]. If our data can be clinically translated, they may lead to an important new nutritional strategy to boost the immune system and decrease the risk of infection that can be a problem in athletes and military personnel who are often exposed to combinations of severe physical, psychological, and environmental stressors. In practical terms, athletes who practice long duration exercises may maintain the stocks of glycogen at more favourable concentrations to perform daily training sessions, by means of ingesting carbohydrate, vitamins, minerals, and β-glucan in the form of oat bran.
In summary, it could be concluded that soluble fibres (i.e. chow rich in oat bran) increased muscular and hepatic glycogen concentrations, and this resulted in a longer time to exhaustion with an associated reduction in pro-inflammatory cytokines. In practical terms, these results demonstrate the importance, not only of the quantity of carbohydrates, but also the balance of dietary fibre content. Further studies conducted in athletes and animal models, using oat bran supplementation are necessary, with the aim of assessing improved performance, in view of the possible positive effects found in the present research.
The authors thank CAPES for the financial support
- Christensen EH: Der Stoffwechsel und die Respiratorischen Funktionen bei schwerer ko¨rperlicher Arbeit. Scand Arch Physiol. 1932, 81: 160-View ArticleGoogle Scholar
- Bergstrom J, Hultman E: A study of glycogen metabolism during exercise in man. Scand J Clin Invest. 1967, 19: 218-10.3109/00365516709090629.View ArticlePubMedGoogle Scholar
- Tarnopolsky MA, Gibala M, Jeukendrup A, Phillips SM: Nutritional needs of elite endurance athletes. Part1: Carbohydrate and fluid requirements. European Journal of Sports Sciences. 2005, 5 (1): 3-14. 10.1080/17461390500076741.View ArticleGoogle Scholar
- American College of Sports Medicine and Dietitians Canada Joint Position Statement. Nutrition and Athletic Performance: Medicine Science and Sports Exercise. 2000, 32 (12): 2130-2145. 10.1097/00005768-200012000-00025.View ArticleGoogle Scholar
- Burke LM, Kiens B, Ivy JL: Carbohydrate and fat for training and recovery. Journal of Sports Sciences. 2004, 22: 15-30. 10.1080/0264041031000140527.View ArticlePubMedGoogle Scholar
- Jeukendrup A: Carbohydrate intake during exercise and performance. Nutrition. 2004, 20: 669-677. 10.1016/j.nut.2004.04.017.View ArticlePubMedGoogle Scholar
- Nieman DC, Davis JM, Henson D, Walberg-Rankin AJ, Shute MCL, Dumke AC, Utter DM, Vinci JA, Carson A, Brown WJ, Lee SR, Mcanulty A, Mcanulty LS: Carbohydrate ingestion influences skeletal muscle cytokine mRNA and plasma cytokine levels after a 3-h run. Journal of Applied Physiology. 2003, 94: 1917-1925.View ArticlePubMedGoogle Scholar
- Kjaer M: Hepatic glucose production during exercise. Advances in Experimental Medicine and Biology. 1998, 441: 117-27.View ArticlePubMedGoogle Scholar
- Mignini F, Traini E, Tomassoni D, Vitali M, Streccioni V: Leucocyte subset redistribution in a human model of physical stress. Clinical Experimental Hypertension. 2008, 30 (8): 720-31. 10.1080/07420520802572333.View ArticlePubMedGoogle Scholar
- Zarkovic M, Ignjatovic S, Dajak M, Ciric J, Beleslin B, Savic S, Stojkovic M, Bulat P, Trbojevic B: Cortisol response to ACTH stimulation correlates with interleukin 6 concentration in healthy humans. European Journal of Endocrinology. 2008, 159 (5): 649-52. 10.1530/EJE-08-0544.View ArticlePubMedGoogle Scholar
- Rivier A: Release of cytokines by blood monocytes during strenuous exercise. International Journal of Sports Medicine. 1994, 15: 192-198. 10.1055/s-2007-1021046.View ArticlePubMedGoogle Scholar
- Moldoveanu AI: Exercise elevates plasma levels but not gene expression of IL1 beta, IL-6, and TNF-alpha in blood mononuclear cells. Journal Applied Physiology. 2000, 89 (4): 1499-504.Google Scholar
- Prestes J, De Ferreira CK, Dias R, Frollini AB, Donatto FF, Cury-Boaventura MF, Guereschi MG, Pithon-Curi TC, Verlengia R, Palanch AC, Curi R, Cavaglieri CR: Lymphocyte and Cytokines after Short Periods of Exercise. International Journal of Sports Medicine. 2008, 29: 1010-1014. 10.1055/s-2008-1038737.View ArticlePubMedGoogle Scholar
- Ostrowski K: Physical activity and plasma interleukin-6 in humans - effect of intensity of exercise. European Journal of Applied Physiology. 2000, 83: 512-515. 10.1007/s004210000312.View ArticlePubMedGoogle Scholar
- Pedersen BK, Steenberg A, Fischer C, Keller C, Keller P, Plomgaard P, Wolsk-Petersen E, Febbraio M: The metabolic role of IL-6 produced during exercise: is IL-6 an exercise factor?. Proceeds of Nutrition Society. 2004, 63: 263-267.View ArticleGoogle Scholar
- Pedersen BK: The anti-inflammatory effect of exercise: its role in diabetes and cardiovascular disease control. Essays Biochemistry. 2006, 42: 105-17. 10.1042/bse0420105.View ArticleGoogle Scholar
- Cox AJ, Pyne DB, Saunders PU, Callister R, Gleeson M: Cytokine responses to treadmill running in healthy and illness-prone athletes. Medicine and Science in Sports and Exercise. 2007, 39 (11): 1918-1926. 10.1249/mss.0b013e318149f2aa.View ArticlePubMedGoogle Scholar
- Puglisi MA, Vaishnav U, Shrestha SW, Torres-Gonzalex M, Wood RJ, Volek JS, Fernandez ML: Raisins and additional walking have distinct effects on plasma lipids and inflammatory cytokines. Lipids in Health and Disease. 2008, 7: 1-14. 10.1186/1476-511X-7-1.View ArticleGoogle Scholar
- Caruso L, Menezes EW: Glycemic index of foods. Journal of Brazilian Society of Food and Nutrition. 2000, 19: 49-64.Google Scholar
- Nieman DC, Pedersen BK: Nutrition and Exercise Immunology Boca Raton. 2000, FL: CRC PressGoogle Scholar
- Davis JM, Murphy EA, Brown A, Carmichael M, Ghaffar A, Mayer EP: Effects of moderate exercise and oat β-glucan on innate immune function and susceptibility to respiratory infection. American Journal of Physiology Integrative and Comparative Physiology. 2004, 286: 366-372.View ArticleGoogle Scholar
- Cavaglieri CR, Martins EF, Colleone VV, Rodrigues C, Vecchia MG, Curi R: Fibre-rich diets alter rat intestinal leukocytes metabolism. Journal of Nutrition and Biochemistry. 2000, 11: 555-561. 10.1016/S0955-2863(00)00118-2.View ArticleGoogle Scholar
- Sampaio-Barros MM: Effect of swimming session duration and repetition on metabolic markers in rats. Stress. 2003, 6 (2): 127-32. 10.1080/1025389031000110169.View ArticlePubMedGoogle Scholar
- Voltarelli FA, Gobatto CA, De Mello MA: Determination of anaerobic threshold in rats using the lactate minimum test. Braz J Med Biol Res. 2002, 35 (11): 1389-94. 10.1590/S0100-879X2002001100018.View ArticlePubMedGoogle Scholar
- Dawson CA, Harvath SM: Swimming in small laboratory animals. Medicine and Science in Sports. 1970, 2: 51-78.PubMedGoogle Scholar
- Siu LO: Determination of glycogen in small tissue samples. Journal of Applied Physiology. 1970, 28 (2): 234-236.Google Scholar
- Sambrook J, Russell DW: Molecular cloning: A laboratory manual. 2001, Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y, A8.21., 3Google Scholar
- Innis MA, Gelfand DH: Optimization of PCRs. In PCR protocols: a guide to methods and applications. Edited by: Innis MA, Gelfand DH, Sninsky JJ, White TJ. 1990, Academic Press, San Diego, CA, 3-12. 1Google Scholar
- Kwok S, Higuch R: Avoiding false positives with PCR. Nature. 1989, 339: 237-238. 10.1038/339237a0.View ArticlePubMedGoogle Scholar
- Czop JK, Austen KF: A. B-glucan inhibitable receptor onhuman monocytes: its identity with the phagocytic receptor for particulate activators of the alternative complement pathway. J Immunol. 1985, 134: 2588-2593.PubMedGoogle Scholar
- Vetivicka V, Thornton BP, Ross GD: Soluble _-glucan polysaccharide binding to the lectin site of neutrophil or natural killer cell complement receptor type 3 (CD11b/CD18) generates a primed state of the receptor capable of mediating cytotoxicity of iC3b-opsonized target cells. J Clin Invest. 1996, 98: 50-61. 10.1172/JCI118777.View ArticleGoogle Scholar
- Sakurai T, Hasimoto K, Suzuki I: Enhancement of murine alveolar macrophage functions by orally administered B-glucan. Int J Immnopharmacol. 1992, 14: 821-830. 10.1016/0192-0561(92)90080-5.View ArticleGoogle Scholar
- Suzuki I, Tanaka H, Kinoshita A, Oikawa S, Osawa M, Yadomae T: Effect of orally administered b-glucan on macrophage function in mice. Int J Immunopharmacol. 1990, 12: 675-684. 10.1016/0192-0561(90)90105-V.View ArticlePubMedGoogle Scholar
- Donatto F, Prestes J, Ferreira CK, Dias R, Frolini A, Leite G, Urtado C, Verlengia R, Palanch A, Perez S, Cavaglieri C: Effects of soluble fibers supplementation on immune system cells after exhausting exercise in trained rats. Rev Bras Med Esporte. 2008, 14 (6): 533-37. 10.1590/S1517-86922008000600011.View ArticleGoogle Scholar
- Pilegaard H, Keller C, Steensberg A, Helge JW, Pedersen BK, Saltin B, Neufer D: Influence of pre-exercise muscle glycogen concentrations on exercise-induced transcriptional regulation of metabolic genes. Journal Physiology. 2002, 54 (1): 261-271. 10.1113/jphysiol.2002.016832.View ArticleGoogle Scholar
- Hays NP, Starling RD, Sullivan DH, Fluckey JD, Coker RH, Williams RH, Evans WJ: Effects of an ad libitum, high carbohydrate diet and aerobic exercise training on insulin action and muscle metabolism in older men and women. Journal of Gerontology A Biological Sciences. 2006, 61 (3): 299-304.View ArticleGoogle Scholar
- Febbraio MA, Keenan J, Angus DJ, Campbell SE, Garnham A: Preexercise carbohydrate ingestion, glucose kinetics, and muscle glycogen use: effect of the glycemic index. Journal of Applied Physiology. 2000, 89: 1845-1851.PubMedGoogle Scholar
- Slavin JL: Dietary fibre and body weight. Nutrition. 2005, 21: 411-418. 10.1016/j.nut.2004.08.018.View ArticlePubMedGoogle Scholar
- Jentjens R, Jeukendrup A: Determinants of post-exercise glycogen synthesis during short-term recovery. Sports Medicine. 2003, 33 (2): 117-44. 10.2165/00007256-200333020-00004.View ArticlePubMedGoogle Scholar
- Wee SL, Williams C, Tsintzas K, Boobis L: Ingestion of a high-glycemic index meal increases muscle glycogen storage at rest but augments its utilization during subsequent exercise. Journal of Applied Physiology. 2005, 99: 707-714. 10.1152/japplphysiol.01261.2004.View ArticlePubMedGoogle Scholar
- Goebel MU, Mills PJ: Acute psychological stress and exercise and changes in peripheral leukocyte adhesion molecule expression and density. Psychmestry Medicine. 2000, 62: 664-670.View ArticleGoogle Scholar
- Gleeson M, Nieman D, Pedersen BK: Exercise, nutrition and immune function. Journal of Sports Sciences. 2004, 22: 115-125. 10.1080/0264041031000140590.View ArticlePubMedGoogle Scholar
- Keller C, Steensberg A, Pilegaard H, Osada T, Saltin B, Pedersen BK, Neufer PD: Transcriptional activation of the IL-6 gene in human contracting skeletal muscle: influence of muscle glycogen concentrations. FASEB Journal. 2001, 15: 2748-2750.PubMedGoogle Scholar
- Lancaster GI, Khan Q, Drysdale PT: Effect of prolonged exercise and carbohydrate ingestion on type 1 and type 2 lymphocyte distribution and intracellular cytokine production in humans. Journal of Applied Physiology. 2005, 98: 565-571. 10.1152/japplphysiol.00754.2004.View ArticlePubMedGoogle Scholar
- Pedersen BK, Febbraio M: Muscle-derived inteleukin-6 - A possible link between skeletal muscle, adipose tissue, liver and brain. Brain, Behavior, and Immunity. 2005, 19: 371-376. 10.1016/j.bbi.2005.04.008.View ArticlePubMedGoogle Scholar
- Steenberg A, Febbraio M, van Hall G, Osada T, Sacchetti M, Saltin B, Pedersen BK: Interleukin-6 production in contracting human skeletal muscle is influenced by pre-exercise muscle glycogen content. Journal Physiology. 2001, 537: 633-639. 10.1111/j.1469-7793.2001.00633.x.View ArticleGoogle Scholar
- Ostrowski K, Rohde T, ASP S, Schjerling P, Pedersen BK: Pro- and anti-inflammatory cytokine balance in strenuous exercise in humans. Journal of Physiology. 1999, 515: 287-291. 10.1111/j.1469-7793.1999.287ad.x.PubMed CentralView ArticlePubMedGoogle Scholar
- Rosa Neto JC, Lira FS, Oyama L, Zanchi N, Yamashita A, Batista M, Oller C, Seelaender M: Exhaustive exercise causes an anti-inflammatory effect in skeletal muscle and a pro-inflammatory effect in adipose tissue in rats. Eur J Appl Physiol. 2009, 106: 697-704. 10.1007/s00421-009-1070-1.View ArticlePubMedGoogle Scholar
- Lira F, Rosa Neto JC, Oyama L, Yamashita A, Batista M, Seelaender M: Endurance training induces depot-specific changes in IL-10/TNF-a ratio in rat adipose tissue. Cytokine. 2009, 45: 80-85. 10.1016/j.cyto.2008.10.018.View ArticlePubMedGoogle Scholar
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