Comparison of erythrocyte and skeletal muscle creatine accumulation following creatine loading
Preen DB, Dawson BT, Goodman C, Beilby J, Ching S
International journal of sport nutrition and exercise metabolism · 5 citas
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Cómo se estudió
- Diseño
- Ensayo controlado aleatorizado (indexado por PubMed)
- Estudiado en
- Personas
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Quién lo pagó
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- Financiación no declarada
Publicación
- Publicado
- 2005-02-01 · Int J Sport Nutr Exerc Metab · vol. 15 · número 1 · págs. 84–93
- Editorial
- Human Kinetics
- Citado
- 7 citas · más que el 55% de estudios similares · 0.2× el promedio de su campo
- Referencias
- 0 trabajos
- Acceso
- De pago
- Áreas de investigación
- Muscle metabolism and nutrition · Biochemical effects in animals · Sports Performance and Training
- Palabras clave
- creatine supplementation, creatine loading, phosphocreatine, total creatine, muscle biopsy, non-invasive biomarkers
- MeSH
- muscle, skeletal, erythrocytes, humans, creatine, phosphocreatine, exercise, administration, oral, cross-over studies, dietary supplements, adult, male
5 autores
- David Brian Preen🇦🇺The University of Western Australia
- BRIAN T. DAWSON
- Carmél Goodman
- John P. Beilby
- Simon Ching
Resumen
El texto original del estudio, en el idioma en que se publicó.
This study attempted to determine the relationship between creatine (Cr) accumulation in human skeletal muscle and erythrocytes following Cr supplementation. If a strong relationship exists, a blood test might provide a practical, less invasive alternative than muscle biopsy for evaluating cellular Cr accumulation. Eighteen active, but not well-trained males were supplemented with Cr (4 x 5 g/d) for 5 d. Muscle biopsies (vastus lateralis) were obtained pre- and post-loading and analyzed for Cr, phosphocreatine (PCr), and total Cr (TCr) content. Venous blood was also drawn at these times to determine erythrocyte Cr concentrations. Muscle Cr, PCr, and TCr concentrations were elevated (P < 0.05) by 39.8%, 7.5%, and 20.1% respectively following supplementation. Erythrocyte Cr concentrations were also elevated (P < 0.01) following the loading period, although to a greater relative degree than tissue concentrations (129.6%). Pre- and post-loading erythrocyte Cr concentrations were poorly and nonsignificantly correlated with that observed in skeletal muscle. Further, loading-mediated increases in erythrocyte Cr concentrations were poorly correlated with elevations in muscle Cr (r = 0.07), PCr (r = 0.06) or TCr (r = 0.04) concentrations. Erythrocyte Cr concentrations can be augmented by 5 d of Cr supplementation, however, this elevation does not reflect that observed in skeletal muscle obtained by muscle biopsy. Consequently, erythrocyte response to Cr loading is not a reliable measure of skeletal muscle Cr/TCr accumulation.
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