ACTN3genotype and modulation of skeletal muscle response to exercise in human subjects
| Autor: | Birgitta Glenmark, Mona Esbjörnsson, Håkan Rundqvist, Ted Österlund, Eva Jansson, Barbara Norman |
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| Rok vydání: | 2014 |
| Předmět: |
Adult
Male medicine.medical_specialty Genotype Physiology Biology Young Adult chemistry.chemical_compound Polymorphism (computer science) Physiology (medical) Internal medicine medicine Humans Actinin Muscle Skeletal Exercise Gene Retrospective Studies Fiber type Glycogen Skeletal muscle Cross-Sectional Studies medicine.anatomical_structure Endocrinology chemistry Female XX Genotype Muscle Contraction |
| Zdroj: | Journal of Applied Physiology. 116:1197-1203 |
| ISSN: | 1522-1601 8750-7587 |
| DOI: | 10.1152/japplphysiol.00557.2013 |
| Popis: | α-Actinin-3 is a Z-disc protein expressed only in type II muscle fibers. A polymorphism in the ACTN3 gene (R577X) results in lack of α-actinin-3 in XX genotype. The prevalence of the mutated X-allele is lower among power/sprint oriented athletes compared with controls, indicating that the lack of α-actinin-3 is detrimental in these sports, but a mechanistic link has not been established. Results from Actn3-knockout (KO) mouse model suggest that α-actinin-3 may affect muscle mass and muscle glycogen levels. In the present investigation we examined muscle fiber type composition, cross-sectional fiber area (CSA), and muscle glycogen levels at baseline in 143 human subjects with different ACTN3 genotypes. In addition, hypertrophy signaling and glycogen utilization in response to sprint exercise were studied in a subset of subjects. Glycogen utilization was analyzed in separate pools of type I and type II fibers. No differences in fiber type composition, CSA, or muscle glycogen levels were observed at baseline across the ACTN3 genotypes. However, the sprint exercise-induced increase in phosphorylation of mTOR and p70S6k was smaller in XX than in RR+RX ( P = 0.03 and P = 0.01, respectively), indicating a less pronounced activation of hypertrophy signaling in XX. Glycogen utilization during sprint exercise varied across ACTN3 genotypes in type II fibers ( P = 0.03) but not in type I fibers ( P = 0.38). The present results are in accordance with findings from the KO mice and reinforce the hypothesis that ACTN3 genotype-associated differences in muscle mass and glycogen utilization provide a mechanistic explanation for the modulation of human performance by the ACTN3 genotype. |
| Databáze: | OpenAIRE |
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