tuneTypical Dose
1000-3000 mg
Amino Acid
L-alanine
tuneTypical Dose
1000-3000 mg
watchEffect Window
No established isolated effect window
check_circleCompliance
WADA NOT PROHIBITED
Overview
Alanine is an amino acid or related metabolite involved in protein turnover and cellular signaling. It is taken to support exercise performance, recovery, or specific metabolic pathways.
Alanine is metabolically important, but isolated oral supplementation has almost no direct human outcome data. Its clearest role is nutritional context rather than a standalone nootropic or performance aid.
Glucose-alanine cycle support and nitrogen transfer. Direct nootropic efficacy as monotherapy remains unproven.
Outcomes
Safety
Evidence
Felig P. The glucose-alanine cycle. Metabolism. 1973;22(2). doi:10.1016/0026-0495(73)90269-2. PMID:4567003.
Population: Review of human and animal studies on the glucose-alanine metabolic cycle
Dose protocol: Review of the glucose-alanine cycle and amino acid metabolism during exercise and fasting states.
Key findings: Establishes alanine's metabolic shuttle role between muscle and liver but provides no evidence for standalone cognitive or performance benefits from isolated supplementation.
Notes: Foundational review of alanine metabolism. No controlled trials of isolated L-alanine for performance or cognition were available at time of publication, and none have emerged since.
This review describes the glucose-alanine cycle, a metabolic pathway in which alanine produced by muscle during amino acid transamination is transported to the liver for gluconeogenesis, with the resulting glucose returning to muscle. The cycle plays a key role in nitrogen transport and glucose homeostasis.
Bodamer OA, Halliday D, Leonard JV. The effects of l-alanine supplementation in late-onset glycogen storage disease type II. Neurology. 2000;55(5):710. doi:10.1212/wnl.55.5.710. PMID:10980742.
Population: Five subjects with late-onset GSD-II and seven healthy controls
Dose protocol: Oral L-alanine supplementation in five patients with late-onset GSD-II and seven healthy controls.
Key findings: L-alanine reduced protein turnover and catabolism in GSD-II patients. The supplement was tolerated at oral doses without reported serious adverse effects.
Notes: One of the few human studies using oral L-alanine as a standalone supplement. Small sample size limits generalizability but supports basic tolerability.
L-alanine supplementation in late-onset GSD-II patients significantly reduced resting energy expenditure, leucine flux, and leucine oxidation compared to healthy controls. These findings indicate that l-alanine reduces protein turnover and catabolism in GSD-II, suggesting a potential therapeutic role in managing this progressive myopathy.