Wilkinson · The Journal of physiology 2008 · Pre-post exercise training intervention study · n=?

Differential effects of resistance and endurance exercise in the fed state on signalling molecule phosphorylation and protein synthesis in human muscle.

Cited 632 times in the scientific literature.

Level 3 - non-randomized controlled study

Non-randomized or unspecified-allocation interventional exercise training study in humans

PubMed 18556367 · doi:10.1113/jphysiol.2008.153916 · record verified 2026-08-29

What was done

In young healthy men in the fed state, researchers measured myofibrillar and mitochondrial protein synthesis rates alongside Akt-mTOR-p70S6K signaling pathway activation at rest and following an acute bout of resistance exercise (RE) or endurance exercise (EE). Measurements were taken in the untrained state and repeated after 10 weeks of dedicated RE or EE training.

What was found

In the untrained state, acute RE increased both myofibrillar (67%, P < 0.02) and mitochondrial protein synthesis (69%, P < 0.02). After 10 weeks of training, RE only increased myofibrillar protein synthesis (36%, P = 0.05). In contrast, EE increased mitochondrial protein synthesis in both untrained (154%, P < 0.05) and trained states (105%, P < 0.05), but did not increase myofibrillar protein synthesis in either state. Acute RE and EE both elevated Akt-mTOR-p70S6K phosphorylation with minor differences between modes, whereas 10 weeks of RE training increased basal Akt-mTOR-p70S6K phosphorylation but EE training did not.

Why it matters

This study demonstrates that chronic training refines muscle protein synthesis from a broad, non-specific response in untrained muscle to a phenotype-specific adaptation tailored to the exercise modality.

Limits

The abstract does not disclose the sample size or whether participants were randomized to training modes. The cohort was restricted to young healthy men, limiting generalizability to women, older individuals, or clinical populations. Upstream signaling phosphorylation failed to fully explain the fraction-specific divergence in protein synthesis.

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