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Effect of Acute Maximal Exercise on Circulating Levels of Interleukin-12 during Ramadan Fasting.
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PMID:  22375234     Owner:  NLM     Status:  PubMed-not-MEDLINE    
Abstract/OtherAbstract:
PURPOSE: The purpose of this study was to examine the effects of Ramadan fasting on circulating levels of interleukin-12 (IL-12) after a brief maximal exercise.
METHODS: NINE SUBJECTS PERFORMED A WINGATE TEST ON THREE DIFFERENT OCCASIONS: (i) the first week of Ramadan (1WR), (ii) the fourth week of Ramadan (4WR), and (iii) three weeks after Ramadan (AR). Blood samples were taken before, immediately and 60 min after the exercise. Plasma concentrations of IL-12 were measured using enzyme-linked immunosorbent assay. Variance analysis revealed no significant effect of Ramadan on P(peak) and P(mean) during the three testing periods.
RESULTS: Considering the effect of Ramadan on plasma concentrations of IL-12, analysis of the variance revealed a significant Ramadan effect (F((2,) (16))=66.27; P < 0.001) as well as a significant time effect (F((2,) (16))= 120.66; P < 0.001). However, no significant (Ramadan × time) of test interaction (F((4,) (32))=2.40; P>0.05). For all measures, IL-12 levels were lower during 1WR and 4WR in comparison with AR (P < 0.05). Considering the exercise effects, IL-12 levels measured immediately after the exercise were significantly higher than those measured before and at 60 minutes after the exercise (P < 0.001).
CONCLUSIONS: These results suggest that an acute intense exercise-induced IL-12 response is modified by daytime fasting and modifications in sleep schedule during Ramadan.
Authors:
Salma Abedelmalek; Nizar Souissi; Akimoto Takayuki; Sami Hadouk; Zouhair Tabka
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Publication Detail:
Type:  Journal Article    
Journal Detail:
Title:  Asian journal of sports medicine     Volume:  2     ISSN:  2008-7209     ISO Abbreviation:  Asian J Sports Med     Publication Date:  2011 Sep 
Date Detail:
Created Date:  2012-02-29     Completed Date:  2012-08-23     Revised Date:  2013-05-29    
Medline Journal Info:
Nlm Unique ID:  101528850     Medline TA:  Asian J Sports Med     Country:  Iran    
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Languages:  eng     Pagination:  154-60     Citation Subset:  -    
Affiliation:
Research Unit, "Performance, Activité Physique et Sportive et Adaptation" Institut Supérieur de Sport et de l'Education Physique, Sfax, Tunisia.
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Journal ID (nlm-ta): Asian J Sports Med
Journal ID (publisher-id): ASJSM
ISSN: 2008-000X
ISSN: 2008-7209
Publisher: Tehran University of Medical Sciences
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© 2011 Sports Medicine Research Center, Tehran University of Medical Sciences
open-access:
Received Day: 06 Month: 11 Year: 2010
Accepted Day: 17 Month: 4 Year: 2011
Print publication date: Month: 9 Year: 2011
Volume: 2 Issue: 3
First Page: 154 Last Page: 160
ID: 3289209
PubMed Id: 22375234
Publisher Id: ASJSM-2-154

Effect of Acute Maximal Exercise on Circulating Levels of Interleukin-12 during Ramadan Fasting
Salma Abedelmalek, PhD12
Nizar Souissi, PhD3*
Akimoto Takayuki, PhD4
Sami Hadouk, PhD5
Zouhair Tabka, PhD2
1Research Unit, “Performance, Activité Physique et Sportive et Adaptation” Institut Supérieur de Sport et de l'Education Physique, Sfax, Tunisia
2Department of Physiology, Sousse Faculty of Medicine, Tunisia
3Research Unit, “Evaluation, Sport, Health” National Centre of Medicine and Science in Sport, Tunisia
4Laboratory of Regenerative Medical Engineering, Centre for Disease Biology and Integrative Medicine, Graduate School of Medicine, The University of Tokyo, Japan
5Department of Immunology, Sfax Faculty of Medicine, Tunisia
*Corresponding Author: Address: Institut Supérieur de Sport et de l'Education Physique de Ksar Saïd. Manouba, 2010, Tunisie. E-mail:n_souissi@yahoo.fr

INTRODUCTION

Interleukin-12 (IL-12) is an immuno-regulatory cytokine [1] that can activate NK cells, generate lymphokine-activated killer cells (LAKs), and induce interferon-γ (IFN-γ) production and T-cell proliferation [2]. Interleukin-12 is a heterodimeric pro-inflammatory cytokine that favours the differentiation of T helper 1 (TH1) cells and forms a link between innate resistance and adaptive immunity. Dendritic cells (DCs) and phagocytes produce IL-12 in response to pathogens during infection [3].

IL-12 has strong anti-tumour activity and has therapeutic use in cancer patients[4]. Furthermore, IL-12 has also been shown to inhibit angiogenesis [5] which will be important during exercise.

During physical exercise, many components of the immune system can be affected according to the nature, frequency, and duration of the exercise [6]. Regular exercise has been reported to have several favourable effects on physiological, psychological, and immunological functions [7] and increase the resistance against infections. Vigorous exercise, however, has been reported to have a negative effect on these functions [8].

It has been generally agreed that circulating numbers of neutrophils and NK cells are markedly increased after strenuous exercise [9]. To the best of our knowledge, there was only one study concerning the changes in IL-12 levels in response to a high-intensity exercise challenge. During this last mentioned study, plasma concentrations of IL-12 increased after a modified Wingate test exercise [10]. Thus, the increase of the plasma concentrations of IL-12 during the Wingate test could indicate that the test can be used to modify immunological states [10].

Furthermore, the physical exercise-induced hyper susceptibility to infections can be amplified by sleep deprivation [11] and caloric restriction [12]. Ramadan fasting could be considered as an ideal hypo-caloric diet [13]. In addition, during Ramadan, the normal sleep-wakefulness cycle associated with the solar day is disrupted [14]. Consequently, the modifications mentioned before can be aggravated during this holy month. Thus, it would be interesting to study changes in circulating levels of cytokine after exercise during Ramadan fasting. In this study therefore, we examined the effect of Ramadan on circulating levels of IL-12 after a brief maximal exercise.


METHODS AND SUBJECTS
Subjects

Nine male students majoring in physical education participated. They were given a thorough explanation of the protocol before signing an informed consent form. Ethical approval for the investigation was secured from the University Ethics committee. The mean (± SD) age and height of the subjects were 22.1 ± 0.2yrs, 176.6 ± 2.5 cm, respectively). The criteria for participant inclusion for this study were that each subject kept standard times for eating prior to the commencement of the study (breakfast at 07:00+1:00 h, lunch at 12:00+1:00 h, and dinner at 20:00+1:00 h) and sleeping habits (sleeping between 23:00 and 07:00+1:00 h). Subjects were non-smokers who did not consume caffeine or alcoholic beverages. They observed the Ramadan fast and abstained from food and liquids from approximately 01:30 to 19:35 for 30 days. At the time of the study, the Ramadan month was from September 12th to October 11th. The length of each fasting day was approximately 16 h.

Experimental Design

During the week before the experiment, all subjects came to the laboratory several times and at different hours of the day to become fully familiarized with the procedure and tests involved so as to minimize learning effects during the experiment.

Then the subjects participated in three weeks of testing, with the experimental protocol comprising three parts: the first week of Ramadan (1WR), the fourth week of Ramadan (4WR), and three weeks after Ramadan (AR). The control trial has been done three weeks after Ramadan because previous studies have shown that anaerobic power [15] and inflammatory and immunological measures [1617] return to the values observed before Ramadan. In each part, all subjects performed a Wingate test. The tests were performed at the same time of the day (10:00 AM) in order to eradicate the effects of the circadian rhythm of IL-12 and performances in the Wingate test. Before the test body weight was measured to the nearest 0.1 kg by using a Tanita digital scale (Tanita, Tokyo, Japan).

Instructions concerning sleep, diet, and physical activity were given to the subjects prior to experimentation. Before the month of Ramadan, participants were synchronized with a nocturnal rest from 23:00+1 h to 07:00. During the month of Ramadan, the participants had to go to sleep before 01:30 and to wake at 07:00 after a night of uninterrupted sleep. All participants kept the same hours of sleep during the three weeks of the experiment.

Compliance to these rules was assessed using the Bastuji and Jouvet calendar throughout the period [18]. The average sleeping time of the participants was 01:50 ± 00:20 h less during the four weeks of fasting than during after Ramadan. During Ramadan, the participants refrained from eating or drinking during the daytime. All meals were eaten at a standard time within the participant's usual schedules and Ramadan customs. There were also dietary restrictions prohibiting any food or drink that could enhance wakefulness, or agents such as alcohol. The participants were required to record their food intakes in a diary over a span of three days for each week of physical testing. The records were analyzed by a nutritionist using a computerized nutrition system, the NUTRISOFT- BILNUT (Vers. 2.01, Paris, France). Throughout the experimental period, participants were requested to maintain their habitual physical activity and avoid strenuous activity during the 24 h before the test sessions. It was easy to control compliance with these directions because all the participants were students who had exactly the same daily schedules in our institution.

Wingate test

The Wingate test involved a 30 sec maximal sprint against constant resistance. For each participant, the load was determined according to body mass using Bar-Or's [19] optimization tables (0.087 kg · kg−1 body mass). Participants were given vigorous verbal encouragement during every test. Seat height was adjusted to each participant's satisfaction and toe-clips were used to prevent the participant's feet from slipping off the pedals. Seat height was recorded and kept the same for each participant throughout the trials. Peak power (Ppeak) was taken as the highest mechanical power elicited during the test. This index was taken as the highest average power during any 5-second period. Mean power (Pmean) was the average power sustained throughout the 30 sec period. The power decrease (Wd) was the difference between the highest and lowest power divided by the highest.

Blood samples

Blood samples were taken from the vein in the antecubital fossa before, immediately after and 60 min after the exercise. Hematocrit and hemoglobin concentrations were obtained using an automated blood cell counter (Symex Kx-21N, Japan) as recommended by Thompson and Dixon [20]. Blood samples were centrifuged at 3000 rpm · min−1 (20 min at 4 °C), and plasma samples were separated and stored at −80 °C until the measurement of IL-12. Prior to statistical analyses, all data except haemoglobin were corrected for changes in plasma volume using the method of Costill and Fink [21].

Measurement of IL-12

Plasma concentrations of IL-12 were measured using an ELISA (Enzyme Linked Immuno-Assay) Kit; Human IL-12 Total ELISA, AbC 261/2, AbCys SA, Paris, France. The intra-assay coefficient of variation was 1.13–7.02%.

Statistical analysis

All statistical tests were processed using Statistica Software (StatSoft, Paris, France). The data were analyzed using analysis of variance (ANOVA). The anaerobic performance parameters were determined using an ANOVA with one factor (Ramadan). The plasmatic parameters were determined using a two-way ANOVA (Ramadan×time). When appropriate, significant differences among means were tested using the least significant difference Post hoc test. The level of statistical significance was set at P < 0.05.


RESULTS
Body Mass and Energy Intake

The ANOVA showed significant effects for Ramadan on body mass (P < 0.001). The body mass was significantly lower in the fourth week of Ramadan in comparison to the other periods of tests. Comparison of mean energy and macro-nutrient intake by the participants during the day in the three different weeks showed significant statistical differences (Table 1).

Wingate test

Analysis of variance revealed no significant effect of Ramadan on the Ppeak and Pmean during the three testing periods (F(2,18) =1,06; P>0.05) (Table 2).

Plasma concentration of interleukin-12

The analysis of variance revealed a significant Ramadan effect (F(2,16)=66.27; P < 0.001) There was also a time effect (F(2,16)=120.66; P < 0.001). However, no significant (time×Ramadan) of test interaction (F(4,32) = 2.40; P>0.05) (Fig. 1).

Concerning the Ramadan effect, plasma concentration of IL-12 measured at before the exercise in 4WR was lower than during 1WR (P < 0.001) and AR (P < 0.001). Moreover, plasma concentration of IL-12 measured at rest was significantly lower during 1WR and AR (P=0.003). Immediately after the exercise (T1), IL-12 levels were lower during 1WR (P=0.01) and 4WR (P < 0.001) in comparison with AR. Moreover, the level of IL-12 immediately after the exercise was significantly decreased in the first week of Ramadan compared to the fourth week of Ramadan (P < 0.001). Similarly, plasma concentration of IL-12 measured 60 minutes after the exercise (T2) decreased during 1WR (P < 0.001) and 4WR (P < 0.001) in comparison with AR.

Concerning the exercise effect during 1WR, 4WR and AR, plasma concentration of IL-12 measured immediately after the exercise was significantly more than those stored at T0 (P < 0.001) and these stored at 60 minutes after the exercise (P < 0.001). However, no significant difference was observed in plasma concentration of IL-12 at (T0) in comparison with 60 minutes after exercise (T2) (P>0.05).


DISCUSSION

This study was designed to determine an acute intense exercise-induced changes in plasma concentrations of interleukine-12 during Ramadan fasting. The results of this study show that the concentrations of IL-12 increase significantly after the exercise during and after Ramadan.

The present study showed that performances during the Wingate test were unaffected by Ramadan. These results are in line with those of the Souissi et al [14] study which showed that the negative effects of Ramadan on anaerobic performance are only observed in the afternoon and evening (17:00 and 21:00 h) and not in the morning.

The results of the present study show that plasma concentrations of IL-12 increased after a maximal anaerobic exercise. These results are in line with those of Akimoto et al [10] during a modified Wingate test. The increase of IL-12 concentrations could be explained by the augmentation of the number of monocytes circulating in response to the maximal exercise. In fact, Ostrowski et al [22] showed an increase in the number of monocytes during strenuous, anaerobic exercise.

The increase of the plasma concentrations of IL-12 during the Wingate test observed in the present study could indicate that this test can be used to modify immunological states [10]. The pro-inflammatory functions of interleukin-12, as well as its ability to stimulate innate resistance and to generate a Th1- type immune response, are essential for resistance to different types of infection. IL-12 is a potent inducer of TH1 responses [23] and it is required for optimal TH1-cell development during the immune response to pathogens [24]. This role of IL-12 has been determined by studying the induction of TH1 responses by recombinant IL-12 in vivo. It is thought that IL-12 directs the generation of the Th1 response via the induction of IFN-γ production, and enhances the cytotoxicity of CD8+ T cells and NK cells [3]. In fact, interferon-γ that is induced by IL-12 has a direct toxic effect on the tumour cells and/or might activate potent anti-angiogenic mechanisms [5].

An important activity of IL-12, acting with IFN- γ and IL-2, is to drive T helper (Th) cell responses toward the Th1 rather than Th2 phenotype [25].

The functions of IL-12 have been studied mainly in terms of lymphocytes, although IL-12 affects other types of cells also. IL-12-induced IFN-γ mediates many of the pro-inflammatory activities of IL-12, whereas the ability of IL-12 to favour a TH1 response exemplifies its function as an immunoregulatory cytokine that bridges innate resistance and adaptive immunity. Not only is IL-12 a potent inducer of IFN-γ production, but it is also required for optimal IFN-γ production in vivo during immune responses, particularly during bacterial or parasitic infections [26,27].

The natural killer (NK) cells show the most pronounced increase after physical exercise [28]. In early studies, it was reported that NK cell activity increased following physical exercise. It is generally agreed that NK cell counts in circulation are increased immediately after Wingate test-type maximal exercise [29].

The decrease of the IL-12 response at the first and the fourth week of Ramadan, before and after the Wingate test, could be, in part, explained by the changes in diet intake during Ramadan fasting such as deficits in vitamin [30]. Indeed, the present study shows significant reduction of vitamins C and E during Ramadan in comparison with the control period. Gleeson et al [31] showed that insufficiencies in vitamins lead to a decrease in the resistance to infections. Similarly, Germano [32] showed that vitamin D deficiency induced a decrease in pro- inflammatory cytokines in particular IL-12.

Partial sleep deprivation can be expected to occur in Ramadan. Recently, Chennaoui et al [16] showed that the Ramadan fasting period is associated with change in sleep habits and increased sleepiness, which may induce inflammatory disturbances. Thus, in this study, repeated partial sleep deprivations can be to the origin of the decrease in plasma concentrations of IL-12 during Ramadan. These results are in line with those of the Dimitrov et al [33] study that showed that sleep deprivation was associated with a decrease in the number of DC producing IL-12, which are a maininducer of Th1 responses. Dinges et al [34] observed that a total deprivation of sleep showed an increase of the non-specific response immunity (the number of phagocytes, the number of NK cells and the activity of the NK cells). Furthermore, Lange et al [35] showed that sleep increases the production of interleukine-12 (IL-12) by the monocytes and inhibited that of interleukine-10 (IL-10), inducing a rhythmicity in the production of these two cytokines.

As we said before, IFN gamma is a potent indicator of a Th1 response which reflects the in vivo function of the altered production of IL-12 by Ramadan fasting. In our study, we would rather measure the plasma level of INF-γ but it is the limitation of the results in our study.


CONCLUSION

In conclusion, our result shows that maximal exercise-induced changes in plasma concentrations of IL-12 during Ramadan are lower than that of after Ramadan. Future studies are needed to explain how Ramadan can modify the IL-12 level after exercise.


ACKNOWLEDGMENTS

The authors wish to express their sincere gratitude to all the participants for their maximal effort and cooperation. This work was supported by the department of immunology, faculty of Medicine, Tunisia. We thank all the technicians of the department of immunology of Hedi Chaker hospital.

Conflict of interests: None


REFERENCES
1. Trinchieri G,Pflanz S,Kastelein RA. The IL-12 family of heterodimeric cytokines: new players in the regulation of cell responsesImmunityYear: 200319641414614851
2. Kobayashi M,Fitz L,Ryan M,et al. Identification and purification of natural killer cell stimulatory factor (NKSF), a cytokine with multiple biologic effects on human lymphocytesJ Exp MedYear: 19893827452504877
3. D'Andrea A,Rengaraju M,Valiante NM,et al. Production of natural killer cell stimulatory factor (interleukin-12) by peripheral-blood mononuclear cellsJ Exp MedYear: 19921761387981357073
4. Noguchi Y,Jungbluth A,Richards EC,Old LJ. Effect of interleukin-12 on tumor induction by 3-methylcholanthreneProc Natl Acad Sci USAYear: 199693117988018876217
5. Voest EE,Kenyon BM,O'Reilly MS,et al. Inhibition of angiogenesis in vivo by interleukin12J Natl Cancer InstYear: 1999875578
6. Petersen AM,Pedersen BK. The anti-inflammatory effect of exerciseJ Appl PhysiolYear: 20059811546215772055
7. Simonson SR. The immune response to resistance exerciseJ Strength Cond ResYear: 2001153788411710669
8. Nieman DC. Exercise infection and immunityInt J Sports MedYear: 199415116238005722
9. McCarthy DA,Dale MM. The leucocytosis of exercise. A review and modelSports MedYear: 19886333633068772
10. Akimoto T,Akama T,Tatsuno M,et al. Effect of brief maximal exercise on circulating levels of interleukin-12Eur J Appl PhysiolYear: 200081510210774876
11. Irwin M,McClintick J,Costlow C. Partial night sleep deprivation reduces natural killer and cellular immune responses in humansFASEB JYear: 199610643538621064
12. Leiper JB,Molla AM. Effects on health of fluid restriction during fasting in RamadanEur J Clin NutrYear: 2003575308
13. Iraki L,Bogdan A,Hakkou F,et al. Ramadan diet restrictions modify the circadian time structure in humans. Study on plasma gastrin, insulin, glucose and calcium and on gastric pHJ Clin Endocrinol MetabYear: 1997821261739100605
14. Afifi ZE. Daily practices, study performance and health during the Ramadan fastR Soc HealthYear: 19971172315
15. Souissi N,Souissi H,Sahli S,et al. Effect of Ramadan on the diurnal variation in short-term high power outputChronobiol IntYear: 200724991100717994351
16. Chaouachi A,Coutts AJ,Wong Del P,et al. Haematological, inflammatory, and immunological responses in elite judo athletes maintaining high training loads during RamadanAppl Physiol Nutr MetabYear: 2009349071519935853
17. Chennaoui M,Desgorces F,Drogou C,et al. Effects of Ramadan fasting on physical performance and metabolic, hormonal, and inflammatory parameters in middle-distance runnersAppl Physiol Nutr MetabYear: 2000345879419767792
18. Bastuji H,Jouvet M. Intérêt de l'agenda de sommeil pour l’étude des troubles de la vigilanceElectroencephalogr Clin NeurophysiolYear: 198560299305 (In Franch). 2579796
19. Bar-Or O. The Wingate anaerobic test an update on methodology, reliability and validitySports MedYear: 19874381943324256
20. Thompson D,Dixon N. Measurement of postprandial interleukin-6 via a catheter: what does it tell us?Eur J Appl PhysiolYear: 2009107621219701768
21. Costill DL,Fink WJ. Plasma volumes changes following exercise and thermal dehydrationJ Appl PhysiolYear: 19743752154415099
22. Ostrowski K,Rohde T,Asp S,et al. Pro and anti-inflammatory cytokine balance in strenuous exercise in humansJ PhysiolYear: 1999515287919925898
23. Manetti R,et al. Natural killer cell stimulatory factor interleukin-12 [IL-12] induces T helper type 1 (TH1)-specific immune responses and inhibits the development of IL-4- producing TH cellsJ Exp MedYear: 19931771199208096238
24. Trinchieri G. Interleukin-12: a cytokine at the interface of inflammation and immunityAdv ImmunolYear: 199870832439755338
25. Hasan M,Najjam S,Gordon MY,et al. IL- 12 is a heparin-binding cytokineJ ImmunolYear: 19991621064709916734
26. Wysocka M,Kubin M,Vieira LQ,et al. Interleukin-12 is required for interferon-( production and lethality in lipopolysaccharide-induced shock in miceEur J ImmunolYear: 19952567267705395
27. Gazzinelli RT,Wysocka M,Hayashi S,et al. Parasite-induced IL-12 stimulates early IFN-( synthesis and resistance during acute infection with Toxoplasma gondiiJ ImmunolYear: 19941532533437915739
28. Gabriel H,Kindermann W. The acute immune response to exercise: what does it mean?Int J Sports MedYear: 1997182845
29. Nielsen HB,Secher NH,Kappel M,et al. Lymphocyte, NK and LAK responses to maximal exerciseInt J Sports MedYear: 19961760658775578
30. Gharbi M,Akrout M,Zouari B. Food intake during and outside RamadanEast Mediterr Health JYear: 200391314015562742
31. Gleeson M,Nieman DC,Pedersen BK. Exercise, nutrition and immune functionJ Sports SciYear: 2004221152514971437
32. Germano C. The Osteoporosis SolutionYear: 1999New YorkKensington Books
33. Dimitrov S,Lange T,Nohroudi K,Born J. Number and function of circulating human antigen presenting cells regulated by sleepSleepYear: 2007304011117520784
34. Dinges DF,Douglas SD,Hamarman S,et al. Sleep deprivation and human immune functionAdv NeuroimmunolYear: 19955971107496616
35. Lange T,Dimitrov S,Fehm HL,et al. Shift of Monocyte Function Toward Cellular Immunity During SleepArch Intern MedYear: 2006166169570016983046

Figures

[Figure ID: F0001]
Fig. 1 

Effect of brief maximal exercise on plasma concentrations of IL-12. The plasma concentration of IL-12 was significantly increased immediately after a Wingate test during the period of Ramadan and after Ramadan.

* Significant difference with before exercise; ¥ significant difference with after Ramadan

1WR: The first week of Ramadan / 4WR: The fourth week of Ramadan: AR: After Ramadan



Tables
[TableWrap ID: T0001] Table 1 

Mean (SD) Values for Daily Nutrient Consumption in the first week of Ramadan (1WR), in the fourth week of Ramadan (4WR) and after Ramadan (AR)


Parameters 1WR 4WR AR
Body Mass (Kg) 74.0 (4.2)* 71.5 (4.4)* 75. 3 (4.4)
Energy (Kcal/Kg/d) 32,9 (3,4)* 31,8 (3,7)* 46,3 (4,2)
Protein (g/d) 74.7 (9.08)* 76.4 (9.2)* 109.2 (17.2)
Protein (%) 12.2 (0.6) 13.4 (0.8) 12.5 (1.1)
Fat (g/d) 79.5 (11.2)* 71.5 (7.3)* 117.6 (13.8)
Fat (%) 29.3 (2.0) 28.2 (1.0) 30.3 (1.7)
Carbohydrate (g/d) 355.7 (33.7)* 319.4 (39.8)* 499.7 (31.5)
Carbohydrate (%) 58.41 (2.5) 56.1 (2.8) 57.2 (1.8)
Vitamin E (mg/d) 11.0 (0.2)* 8.9 (0.1)* 14.3 (0.1)
Vitamin C (mg/d) 41.4 (1.1)* 36.2 (0.9)* 51.7 (1.1)

*Significant difference in comparison with after Ramadan/SD: Standard Deviation


[TableWrap ID: T0002] Table 2 

Mean (ES) values for Ppeak and Pmean (n = 12) in the first week of Ramadan (1WR), in the fourth week of Ramadan (4WR) and after Ramadan (AR)


Parameter 1WR 4WR AR
Ppeak(W/kg) 9.80 (0.8) 9.7 (0.3) 10.2 (0.6)
Pmean(W/kg) 7.7 (0.2) 7.8 (0.2) 8.1 (0.5)
Fatigue index (%) 42.1 (3.5) 43.7 (4.2) 41.4 (4.8)

ER: Error Standard



Article Categories:
  • Original Article

Keywords: Ramadan, Wingate Test, Interleukin-12, Immunity, Sleep Deprivation.

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