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Print version ISSN 1517-8692
Rev Bras Med Esporte vol.13 no.5 Niterói Sept./Oct. 2007
Creatine supplementation and strength training: alterations in the resultant of dynamic maximum strength and anthropometric variables in college students submitted to 8 weeks of strength training (hypertrophy)
Tácito Pessoa de Souza JúniorI, IV; João Paulo DubasIII; Benedito PereiraII; Paulo Roberto de OliveiraIV
Universidade Metropolitana de Santos Faculdade de Educação
IIEEFUSP Escola de Educação Física e Esporte da Universidade de São Paulo
IVUNICAMPFEF Universidade Estadual de Campinas Faculdade de Educação Física
To verify the alterations promoted by creatine supplementation in the anthropometric
variables and the resultant of dynamic maximum strength (RDMS) in college students
submitted to 8 wk of strength training.
METHODOLOGY: The sample consisted of 18 male college students, aged between 19 to 25 years. Height (cm), body mass (kg) and tests of maximum voluntary muscular action (1MVMA) weight in the squat were determined prior to the training. The subjects were divided in two groups: A (creatine) or B (placebo). The doubleblind protocol was adopted. After 8 weeks of strength training, the tests battery from the pretraining was repeated.
RESULTS: After 8 wk of training, it was verified that both groups had statistically significant (SS) alterations in the RDMS in all the exercises (p = 0.007 / 0.008). The analysis of the percentile improvement (PI) and the RDMS delta in the squat exercises, military press and closegripextensions, showed that group A had positive SS alterations higher than group B (p = 0.008 / 0.038). Lean body mass only SS increased in group A (p = 0.038). However, the percentage of body fat did not show alterations in none of the groups. The relationship between the PI of the arm and forearm circumferences (C) and the PI in the RDMS of the development exercise was SS (r = 0.481 and 0.546, respectively), as well as between the PI in the thigh C and the PI of the RDMS of the squat exercise (r = 0.619).
CONCLUSION: Regardless the substance ingested, strength training was able to increase in RDMS; however, creatine supplementation was shown to be more efficient that the placebo, showing higher percentual and delta improvement in strength.
Keywords: Sports nutrition. Physical training. Ergogenic aid.
Due to the increase of commercialization of nutritional products with the purpose to play an ergogenic effect in sports performance, many physical activities practitioners, especially bodybuilders, have been using them in order to promote strength and muscular mass increase. Thus, several nutritional supplements can be found in the market, from amino acids to zinc, which have been sold as effective ergogenics for physically active individuals. With a few exceptions, such as the carbohydrates supercompensation (overload), wellelaborated research does not support the ergogenic effect for the majority of the nutritional supplements when added to a healthy and suitable diet(13).
In the end of the 80's and beginning of the 90's, creatine supplementation (Cr) has been an important ergogenic aid in the worldwide sports scenario, as well as for practitioners of endurance exercises with the purpose to increase strength and muscular mass(45). The success of British runners and jumpers in the beginning of the 90's was associated with Cr supplementation(3,67). Nowadays, this practice has been used by many athletes with maximal strength, explosive strength and velocity, such as bodybuilders, fighters, cyclists, footballers, swimmers, amateur and professional athletes and fitness centers goers.
According to what has been discussed in the investigations by Pereira and Souza Junior(810), the term adaptation should not be used to explain structuralfunctional alterations concerned with physical training, once they are reversible. Therefore, we have adopted the term alteration to explain the alterations occurred in this study.
According to proposals by Phillips(11), also supported by Pereira and Souza Júnior(910,12) and Souza Junior et al.(1314), the correct use of the terminology applied to the maximal load test would be 'Maximal Voluntary Muscular Action' (MVMA), which will be able to evaluate the highest strength voluntarily generated by a maximal dynamic voluntary muscular action (MDVMA) or maximal static voluntary muscular action (MSVMA). Although the terminology proposed by DeLorme and Watkins(15) is internationally accepted (1RM), the understanding of 'repetition' would be showing more than one performance and, since we are expressing the maximal muscular action in a single movement, we will be using in this investigation the terminology proposed here. However, when the number of bouts is equal or higher than two, we will be using the terminology maximal repetition (MR).
The aim of this study was to verify the alterations promoted in the anthropometric variables and in the maximal dynamic strength resultant (MDSR) between the creatine supplemented and placebo groups, after 8 weeks of strength training (hypertrophy).
Eighteen male university students, aged 1925 years were volunteers in this study. The inclusion criteria were: (a) to have practical experience of at least 1 (one) year in overload exercises; (b) not to smoke and/or drink alcohol; (c) not to make use of androgenic anabolic steroids or similar substances and (d) not to present pathological history. The study was approved by the Ethics Committee of the College of Medical Sciences of UNICAMP (Project: # 260/2005 CAAE: 0078.0.146.00005), according to the norms of the Resolution 196/96 from the National Health Board on research involving humans.
After having signed a written consent form, the aims and procedures of the study, as well as the involved risks were explained. After the tests battery, the subjects were randomly placed in one of the two groups of the study: creatine group (A; n = 09) and placebo group (B; n = 09).
Evaluation protocol of the maximal dynamic muscular strength resultant
The 1MDVMA tests for exercises of the upper and lower extremities were performed at different days, so that the volunteers could have a longer recovery interval between tests.
1MDVMA test for the bench press exercise
For the 1MDVMA test performed in the bench press exercise (flat and incline), the volunteers had a previous warmup and could perform three tries (when not determined in a single try) to determine the 1MDVMA. It was considered 1MDVMA when the volunteer was able to repeat a complete movement, having the elbow flexion until the bar touched the chest and immediately after, extending elbow until returning to initial position, using its maximal dynamic voluntary strength, with no external aid (only for safety) of the proposed exercise. In case the volunteer was able to repeat the same movement more than once, the test was stopped and after 5 minutes of rest, it was resumed with load increase to the exercise.
1MDVMA test for the squatting exercise
The 1MDVMA determination in the squatting exercise was measured with simultaneous knee flexing, with the barbell rested on shoulders until reaching a 90° angle. For volunteers' safety, a bench was placed behind each of them, so that they could bend knees until the proposed angle and immediately return to initial position, as soon as the gluteus touched the bench. It was considered 1MDVMA when the volunteer, using his maximal volunteer strength, was able to bend knees until touching the gluteus on the bench and return to initial position without external help (just for safety).
1MDVMA test for knee flexion and extension exercises
The remaining exercises for lower extremities, knee flexion and extension, were performed with specific machines (extensor chair and flexor table), always with three tries for determination of the 1MDVMA and always with 5minute rest between tries, in case the test had not been determined in a single try.
1MDVMA test for shoulder exercises
In the exercises selected for the shoulders (development and lateral arms lift), the volunteers were instructed to perform 1MDVMA without body balancing ('stolen' repetition), totally starting from inertia. The 1MDVMA test for development was performed as following: a) the volunteer was helped to remove the barbell from the ground with the aid of the evaluators; b) the barbell was placed on the posterior part of the deltoids; and c) the volunteers should lift the proposed load in a single time, making total elbow extension without external help. In the determination of 1MDVMA for the lateral arms lift exercise, the subject started the movement with the dumbbells touching the thigh, in total inertia, making abduction of upper extremities up to the shoulders height. In case there was need for another try, the procedure would be performed according to what was previously described.
1MDVMA test for arm exercises (biceps and triceps)
The exercises called 'barbell curl' and 'dumbbell curl' elbow flexion with forearms lift in prone position, lifting the barbell towards the trunk and elbow alternated flexion with forearm lift in prone position with wrist rotation for the exterior, lifting the dumbbell towards the shoulder, respectively, were also performed with the movement starting from initial position, with total lack of movement. In order to determine 1MDVMA in the selected exercises for the triceps, pulley triceps extension and closed bench press, respectively, the volunteers performed the following procedures: a) pulley triceps: the volunteers faced the machine and were told to perform 1MDVMA extending the elbow, holding the barbell with the two hands and returning to initial position without external help; b) closed bench press: the volunteers started the exercise laid on the bench, holding the barbell with a slight space between hands (distance between thumbs), removing the barbell from the rest with the evaluators' aid and performed 1MDVMA, flexing the elbow until the barbell touched the chest and later extending the elbow until initial position without external help (only for safety).
1MDVMA test for torso muscles
In order to determine the 1MDVMA value in the exercise for the torso muscles performed in the frontal pulldown, the volunteers seated facing the machine, holding the barbell on the extremities with extended elbows, and at the evaluator's command, performed elbows flexion, approaching the barbell towards the torso until touching it, using his maximal dynamic voluntary strength without external interference. In the determination of 1MDVMA in the low row exercise, the volunteer seated on the ground, knees slightly flexed and feet resting on the specific foot rest from the machine, extended elbows and holding the triangle. At the evaluator's command, the volunteer flexed the elbow, together with the shoulder extension, until touching the triangle on the torso, using his maximal dynamic voluntary strength.
1MDVMA tests for the abdomen
In the abdominal exercise (crunch), the 1MDVMA test was performed with volunteers facing the pulley, seated on their ankles, holding the triangle with fleeted elbows and flexing the spine until the elbows would touch the knees. In case other tries were needed, the procedures were equal to the ones previously described for all exercises.
The 1MDVMA load determination was performed in the pre and posttraining.
Strength training protocol
The training protocol was applied during 8 weeks. During the two first weeks (Phase A) the training had the aim to provide neuromuscular adjustments in the students; in the six subsequent weeks (Phase B) the training aimed to increase the MSR and muscular mass (hypertrophy).
The training was performed in 6 weekly sessions, from Monday to Saturday. Free weights and machines were used and the training was supervised by a group of students especially prepared for the task. Phase A consisted of exercises performed at 50% of 1MDVMA, with 120second pause between them (table 1 and table 2). Phase B consisted of exercises at 80% of 1MDVMA, performing 4 bouts with 8 to 10 repetitions with 120second pause between exercises from one muscular group to another (table 3, table 4, table 5). The pauses were decreasing during the subsequent training weeks, according to the protocol proposed by Souza Junior(1314,16), illustrated in table 6.
The protocol proposed by Souza Junior(16), from the study by Volek et al.(17) was applied. During the 3rd week of training (Phase B) the subjects from group A ingested 30 g of monohydrated creatine (CrH2O) a day, divided in five equal doses of 5 g at 3 to 4hour intervals. From week 4 to 8, 5 g of monohydrated creatine a day were administered, which corresponded to the maintenance phase. Group B received the same supplementation profile, where the placebo used was maltodextrine.
CrH2O was kindly provided by the Pro Tech Nutritional Systems of Brazil, while the placebo substance was bought at a store from the nutritional supplements market. The substances were stored and labeled in 0.5 g capsules by Pedrosa & Delsin Pharmacy LTDA. Neither the subjects nor the researchers would know which substance was being ingested until the end of the study.
Anthropometric measurement protocol
The anthropometric measurement was determined through weight, height, measurement of eight skinfolds and eight circumferences. The adopted procedures and materials are as follows:
For weight measurement, a Filizola mechanical with 0.1 kilogram scale was used. After the scale calibration, the subject would wear the minimum clothes as possible and stand in the center of the scale. The reading was performed when the scale lever reached balance. Weight was registered in kilograms (kg), with precision of 100 grams(18).
For height determination, Sanny mobile stadiometers with scale in 0.1 centimeter (cm) were used. According to Petroski(18), height comprises the distance between the vertex (highest point of the head) and the feet soles, with head being according to the Frankfurt plan. The subject would be barefeet or wearing socks and stand keeping heels, pelvic waist, scapular waist and occipital region touching the stadiometers; after the subject performed a maximal inspiration followed by apnea, height was registered in centimeters, with 0.1 cm precision.
For skinfolds measurement, a Lange adipometer with 1 millimeter scale (mm) and steady pressure in 10 grams per square millimeter (g/mm2) was used. The procedures described by Heyward and Stolarczyk(19) for determination of the eight skinfolds adopted were: subscapular skinfold, tricipital skinfold, medium axillary skinfold, torso skinfold, suprailiac skinfold, abdominal skinfold, thigh skinfold and medial calf skinfold, being them measured on the right side of the body and repeated three times in each point in rotational order.
For the circumferences determination, a Sanny metallic measuring tape with scale in 0.1 cm was used. The procedures presented by Heyward and Stolarczyk were followed(19).
Body fat percentage estimation
For estimation of the body density, the sum of seven skinfolds was used, namely: subscapular, tricipital, torso, medium axillary, suprailiac, abdominal and thigh. This sum was applied in the equation developed by Jackson and Pollock (1978) apud Petroski(18).
After determination of the body density, the equation by Siri (1961) apud Petroski(18), was used for determination of the body fat percentage.
The ShapiroWilk statistical proof was applied, as well as the inspection of the quantis charts (qqplot) in order to determine whether the dependent variables (BM, BMI, MDSR) followed or could be rounded up by the normal distribution. Once these variables could not be rounded up by the normal distribution, nonparametric statistics were chosen to be applied for description and inference of the observations.
Quartis 1, 2 and 3 were calculated as indicators of the central position measurement (quartil 2 or median) and the dispersion (quartis 1 and 3, as well as interquartil interval).
The nonparametric hypothesis analysis defined by Brunner and Langer was applied(20) in order to verify the significance of the difference between groups A and B, between pre and posttraining, as well as the interaction between these factors. The statistical significance was accepted in a £ 0.05.
In table 7 the anthropometric characteristics of the volunteers in each of the groups are described. According to what was described in this table, no statistically significant differences have been verified between groups A and B in any of the training moments for all anthropometric variables (BM, S8SF, BFP and FFM). However, when analyzing the training and used supplement effects, it was possible to observe that the group which made use of CrH2O presented statistically significant increase for BM and FFM, without significant alterations in the body fat profile. On the other hand, for the placebo group the alterations observed in these variables may be concerned with causal variations and not with training effects.
Besides the effect observed in the BM and FFM, concerning training for the creatine group, significant interaction between supplement and training was obtained for these variables, according to what was described in figure 1 and figure 2. When the supplement effect on the absolute and percentage BM alteration was analyzed, it was observed that the creatine group had alteration significantly higher than that obtained by the placebo group. The FFM percentage alteration was significantly higher in the creatine group comparing to the placebo group. For the BFP and S8SF statistically differences were not observed between groups, neither for absolute nor percentage alteration.
Alteration in the maximal dynamic strength resultant
The MDSR analysis showed that both groups improved significantly the maximal dynamic strength profile in all exercises (bench press, closed bench press, barbell curl, development and squatting). Moreover, significant differences between creatine and placebo groups have not been observed neither in the pre nor the posttraining, according to table 8.
Although significant differences between the groups have not been obtained when the absolute values of the MDSR in the different exercises are analyzed, the response of the absolute and relative alteration in the closed bench press, development and squatting exercises showed that the creatine group presented alterations significantly higher than those obtained in the placebo group. However, in straight seat bench press and the dumbbell curl exercises, there was not evidence that the observed differences between both groups could be due to the supplement used (figure 3 and figure 4).
The alterations both in groups A (creatine) and B (placebo) are due to modifications of the biological processes which occur in the body when it is submitted to strength training. Based mainly in the principles of overload and specialization, the physical training has been frequently organized so that it allows that the body energy supplies, as well as the processes responsible for their production are maximized(8). According to Viru(2122), this phenomenon is known as supercompensation. The imposing of work loads using the protocol of 80% of 1MDVMA, as demonstrated in this investigation, allowed to observe that regardless the nutritional supplementation used as ergogenic resource, these positive alterations occur more significantly. Nevertheless, the results of this study corroborate with others(16,2328), where positive alterations were found in the anthropometric variables (BMI, BM) and in the increase of the MDSR, confirming the theory that the CrH2O supplementation can promote positive physiological and biochemical alterations in the organism, causing morphological benefits and consequently promoting improvement in physical and sportive performance. Recent evidence demonstrated by Haussinger and Lang(29) and Haussinger et al.(30) show that the increase of the cellular volume is modulated by amino acids and hormones which regulate the activities of the transporter ions and the ionic channels present in the plasmatic membrane, affecting the potential of the membrane or regulating the substrates that are transported by dependence of Na+. Specifically, the anabolic effect of the hormone insulin and the anticatabolic effect of the amino acid glutamine may alter the cellular volume. This idea is supported by the fact that the anabolic effects are able to be quantitatively minimized by cells hydrated in hypoosmotic medium. According to Kreider(24); Ziegenfuss et al.(31); Vandenberghe et al.(32); Haussinger et al.(30); Bessman and Savabi(33) this alteration may be interpreted as one of the factors responsible for the increase of proteins synthesis (anabolism) or by the reduction of the protein degradation (catabolism), or when these mechanisms are observed associated with creatine supplementation. Corroborating this theory, Ingwall(34) has reported that the creatine addition to incubated skeletal muscular cells increases the in vitro myosin synthesis.
The literature is scarce on studies comparing strength gains and hypertrophy in the elbow flexor muscles (biceps). The results presented by Becque et al.(35), when evaluating the elbow flexors with the 1MDVMA test evidenced positive alterations in both groups (p = 001), with the creatine group presenting significantly positive alteration higher than the placebo group (16.77% against 6.25%, respectively). Vandenbergue et al.(32) compared the torque of elbow flexors in healthy bur sedentary women, in 5 bouts of 30 maximal voluntary repetitions with 2minute interval between bouts. However, significant differences were not found between the creatine and placebo groups (n = 19). Corroborating the specificity principle, the positive alterations caused by strength training with muscular hypertrophy joined with CrH2O supplementation as purpose do not seem to demonstrate positive alterations, when the training uses local muscular resistance protocols (LMR).
Based on the results presented in this study it is concluded that the training protocol proposed can promote positive alterations in the MDSR regardless the use of any ergogenic agent. Nevertheless, when joined with creatine supplementation, the positive alterations in the MDSR, as well as in weight, were more significant comparing with the placebo group.
It is suggested that in future studies the used protocol with decreasing pauses is compared with other protocols with different methodological design, and that the effects of creatine supplementation are verified together with carbohydrates supplementation, making use of other technologies, such as Magnetic Resonance. Additionally, the supplementation effects should be evaluated at cellular level.
1. Brazilian Society of Sports Medicine: Dietary changes, fluid replacement, food supplements and drugs: demonstration of ergogenic action and potential health risks. Rev Bras Med Esporte. 2003;9:43-56. [ Links ]
2. Tarnopolsky MA, Gibala M, Jeukendrup AE, Phillips SM. Nutritional needs of elite endurance athletes. Part I: carbohydrate and fluid requirements. Eur J Sports Sci. 2005;5:3-14. [ Links ]
3. Williams MH, Kreider RB, Branch JD. Creatina. São Paulo: Manole; 2000. [ Links ]
4. The American College of Sports Medicine. Roundtable: The physiological and health effects of oral creatine supplementation. Med Sci Sports Exerc. 2000; 32:706-17. [ Links ]
5. Mesa JLM, Ruiz JR, Gonzales-Gross MM, Sainz AG, Castillo Garzon MJ. Oral creatine supplementation and skeletal muscle metabolism in physical exercise. Sports Med. 2002;32:903-44. [ Links ]
6. Wyss M, Kaddurah-Daouk R. Creatine and creatinine metabolism. Physiol Rev. 2000;80:1107-213. [ Links ]
7. Bemben MG, Lamont HS. Creatine supplementation and exercise performance. Sports Med. 2005;35:107-25. [ Links ]
8. Pereira B, Souza Junior TP. Dimensões biológicas do treinamento físico. São Paulo: Phorte; 2002. [ Links ]
9. Pereira B, Souza Junior TP. Compreendendo a barreira do rendimento físico. São Paulo: Phorte; 2005a. [ Links ]
10. Pereira B, Souza Junior TP. Adaptação e rendimento físico considerações biológicas e antropológicas. Rev Bras Cien Mov. 2005b;13:145-52. [ Links ]
11. Phillips SM. Short-term training: when do repeated bouts of resistance exercise become training? Can J Appl Physiol. 2000;25:185-93. [ Links ]
12. Pereira B, Souza Junior TP. Metabolismo celular e exercício físico. Aspectos bioquímicos e nutricionais. São Paulo: Phorte; 2004. [ Links ]
13. Souza Junior TP, Dubas JP, Pereira B, Oliveira PR. Effect of creatine supplementation in the maximum strength of the bench press exercise in college students after 8 weeks of training. FIEP Bulletin. 2005a;75:562-5. [ Links ]
14. Souza Junior TP, Dubas JP, Pereira B, Oliveira PR. The effect of the creatine supplementation in the maximum dynamic strength of the squatting exercises in college students after eight weeks of training. FIEP Bulletin. 2005b;75:558-61. [ Links ]
15. DeLorme TL, Watkins A. Techniques of progressive resistance exercise. Arch Phys Med. 1948;29:263-73. [ Links ]
16. Souza Junior TP. Suplementação de creatina e treinamento de força: alteração da resultante de força máxima maximorum, hipertrofia muscular e variáveis antropométricas. [Dissertação de Mestrado em Ciências do Esporte]. Campinas: Faculdade de Educação Física, Universidade Estadual de Campinas; 2002. [ Links ]
17. Volek JS, Duncan ND, Mazzetti SA, Staron RS, Putukian M, Gomez AL, et al. Performance and muscle fiber adaptations to creatine supplementation and heavy resistance training. Med Sci Sports Exerc. 1999;31:1147-56. [ Links ]
18. Petroski EL. Desenvolvimento e validação de equações generalizadas para a estimativa da densidade corporal em adultos. [Tese de Doutorado em Educação Física]. Santa Maria: Centro de Educação Física e Desportos, Universidade Federal de Santa Maria; 1995. [ Links ]
19. Heyward VH, Stolarczyk LM. Applied body composition assessment. Champaign: Human Kinetics; 1996. [ Links ]
20. Brunner E, Langer F. Nonparametric analysis of ordered categorical data in designs with longitudinal observations and small sample sizes. Biometrical J. 2000; 42(6):663-75. [ Links ]
21. Viru A. Mobilization of the possibilities of the athlete's organism: a problem. J Sports Med Phys Fitness. 1993; 33:413-25. [ Links ]
22. Viru A. Differences in effects of various training regimes on metabolism of skeletal muscles. J Sports Med Phys Fitness. 1994;34:217-27. [ Links ]
23. Volek JS, Kraemer WJ, Bush JA, Boetes M, Incledon T, Clark KL, et al. Creatine supplementation enhances muscular performance during high-intensity resistance exercise. J Am Diet Assoc. 1997;97:765-70. [ Links ]
24. Kreider RB, Ferreira M, Wilson M, Grindstaff P, Plisk S, Reinhardy J, et al. Effects of creatine supplementation on body composition strength, and sprint performance. Med Sci Sports Exerc. 1998;30:73-82. [ Links ]
25. Green AL, Simpson EJ, Littlewood JJ, MacDonald IA, Greenhaff PL. Carbohydrate ingestion augments creatine retention during creatine feeding in humans. Acta Physiol Scand. 1996;158:195-202. [ Links ]
26. Soderlund K, Balsom PD, Ekblom BP. Creatine supplementation and high intensity exercise: influence on performance and muscle metabolism. Clin Sci. 1994; 87:120-1. [ Links ]
27. Balson PD, Ekblom B, Soderlund B, Sjodin B, Hultman E. Creatine supplementation and dynamic high-intensity intermittent exercise. Scand J Med Sci Sports Exerc. 1993;3:143-9. [ Links ]
28. Birch R, Noble D, Greenhaff PL. The influence of dietary creatine supplementation on performance during repeated bouts of maximal isokinetic cycling in man. Eur J Appl Physiol. 1994;69:268-70. [ Links ]
29. Haussinger D, Lang F. Cell volume in the regulation of hepatic function: a mechanism for metabolic control. Biochem Biophys Acta. 1991;1071:331-50. [ Links ]
30. Haussinger D, Roth E, Lang F, Gerok W. Cellular hydration state: An important determinant of protein catabolism in health and disease. Lancet. 1993;341:1330-2. [ Links ]
31. Ziegenfuss TN, Lowery LM, Lemon PWR. Acute fluid volume changes in men during three days of creatine supplementation. JEPonline. 1998;1:1-9. Available at: http://css.edu/users/tboone2/asep/jan13d.htm. [ Links ]
32. Vandenberghe KM, Goris M, Van Hecke P, Van Leemputte M, Vangerven L, Hespel P. Long-term creatine intake is beneficial to muscle performance during resistance training. J Appl Physiol. 1997;83:2055-63. [ Links ]
33. Bessman SP, Savabi F. The role of the phosphocreatine energy shuttle in exercise and muscle hypertrophy. In: Biochemistry of Exercise VII. Champaign, IL: Human Kinetics; 1990. p. 167-77. [ Links ]
34. Ingwall JS, Weiner CD, Morales MF, Davis E, Stockdale FE. Specificity of creatine in the control of muscle protein synthesis. J Cell Biol. 1974;63:145-51. [ Links ]
35. Becque MD, Lochmann JD, Melrose DR. Effects of oral creatine supplementation on muscular strength and body composition. Med Sci Sports Exerc. 2000; 32:654-8. [ Links ]
Correspondence to: Approved in 14/6/07. All the authors
declared there is not any potential conflict of interests regarding this article.
Rua Roberto Sandall, 28, apto. 72
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Approved in 14/6/07.
All the authors declared there is not any potential conflict of interests regarding this article.