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Ensayo controlado aleatorizado1998Financiación no declarada

Creatine and caffeine in anaerobic and aerobic exercise: effects on physical performance and pharmacokinetic considerations

Vanakoski J, Kosunen V, Meririnne E, Seppälä T

International journal of clinical pharmacology and therapeutics · 29 citas

Etiquetas de revisión

Financiación no declarada

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Cómo se estudió

Diseño
Ensayo controlado aleatorizado (indexado por PubMed)
Estudiado en
Personas
Resultado principal
Marcadores de salud y funcionamiento

Quién lo pagó

Financiación
Financiación no declarada

Publicación

Publicado
1998-05-01 · Int J Clin Pharmacol Ther · vol. 36 · número 5 · págs. 258–62
Editorial
National Institutes of Health
Citado
52 citas · más que el 70% de estudios similares · 0.8× el promedio de su campo
Referencias
1 trabajos
Acceso
De pago
Áreas de investigación
Muscle metabolism and nutrition · Coffee research and impacts · Sports Performance and Training
Palabras clave
creatine supplementation, caffeine, anaerobic exercise, aerobic exercise, physical performance, pharmacokinetics, trained athletes, cycling performance, blood lactate, heart rate, post-exercise recovery
MeSH
humans, creatine, caffeine, central nervous system stimulants, exercise, administration, oral, area under curve, cross-over studies, double-blind method, physical endurance, adolescent, adult, female, male

4 autores

  • Jyrki Vanakoski🇫🇮University of Helsinki
  • Valtteri Kosunen
  • Esa Meririnne
  • Toni T. Seppälä

Resumen

El texto original del estudio, en el idioma en que se publicó.

The pharmacokinetics and effects of creatine and caffeine administration on anaerobic and aerobic performance of 7 trained athletes were studied in a randomized, placebo-controlled, double-blind crossover design. The treatments were: placebo (PLA), a single oral dose (7 mg x kg(-1)) of caffeine (CAF), repeated oral doses (3 x 100 mg x kg(-1) x day(-1)) of creatine for 3 days (CRE), or the combination of caffeine and creatine (CAF + CRE) before physical exercise. In one session CAF was administered without exercise. Drug administration was followed by 3 repetitive 1-minute exercise bouts on a bicycle ergometer at maximal speed (anaerobic exercise) starting 70 min after drug administration. Anaerobic exercise was followed by 45 min of cycling at constant pedalling speed and workload (aerobic exercise). CRE and CAF, alone or in combination, did not improve maximal pedalling speed (rpm), maintenance of maximal speed (rpm) or total work output (kJ) during the 1 -minute bouts, when compared with PLA. In addition, no statistically significant differences in heart rate or blood lactate were observed between the treatments either during anaerobic or aerobic exercise bouts. Creatine was rapidly and efficiently absorbed, as reflected by plasma concentrations. The mean +/-SEM value for creatine Cmax was 1.22+/-0.14 mmol x l(-1), tmax 92+/-7 min and plasma half-life (t1/2beta) 172+/-21 min. Caffeine pharmacokinetics were not affected by concomitant administration of creatine or by physical exercise. In conclusion, neither maximal performance and subsequent recovery nor aerobic performance were enhanced by oral creatine supplementation in the study.

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