Creatine

Overview
Creatine is a nitrogen-containing compound that plays a critical role in cellular energy metabolism, particularly in tissues with high energy demands like the brain and muscles. It functions through the phosphocreatine system, which acts as a rapid energy buffer to recycle ATP, the primary energy currency of cells. In the brain, creatine helps support high-energy demand processes such as neurotransmitter synthesis, ion pumping, and synaptic transmission. It enhances mitochondrial energy buffering and supports cognitive function, particularly under conditions of increased cognitive load or energy stress.
Recipes
Foods
Biological Mechanisms and Implications
References
- Creatine supports ATP recycling via the phosphocreatine system and enhances working memory and cognitive processing speed, particularly under cognitive load Avgerinos et al. 2018
- Creatine supplementation improves cognitive performance in sleep-deprived adults McMorris et al. 2007
- Combinations of creatine and CoQ10 show additive neuroprotection in models of Parkinson's and Huntington's disease Yang et al. 2009
- While omnivore diets naturally supply creatine from beef, lamb, pork, salmon, tuna, cod, and scallops, vegan diets contain minimal amounts, making supplementation or fortified foods necessary for plant-based eaters
Foods supply the named dietary input. They are not shown as containing the downstream metabolite. Conversion evidence does not establish a new downstream PM admission, effective dose or equivalent food intervention.
Arginine → Human AGAT transfers the amidino group of arginine to glycine, yielding guanidinoacetate and ornithine. → GAMT methylates guanidinoacetate using S-adenosylmethionine to form creatine. → Creatine
BRS4-FM1-PM3: Enable rapid ATP buffering so high-energy-demand tissues can meet sudden metabolic spikes.
Existing admission: Type A / derived; versioned-assessment. The complete derived relationship is admitted for this PM.
Capacity of the endogenous synthesis route is distinct from a claim that extra amino-acid intake raises cerebral creatine, phosphocreatine buffering or cognition. AGAT feedback, GAMT methyl supply, organ exchange and SLC6A8-mediated tissue transport constrain delivery. Human renal GAA production is not a measurement of brain synthesis flux; rat arginine infusion and glycine null responses are not oral human efficacy experiments.
- Lupin Beans — supplies Arginine; verified; raw. Lupins, mature seeds, raw
Composition provenance
USDA SR Legacy April 2018
- Watermelon — supplies Arginine; verified; raw. Watermelon, raw
Composition provenance
USDA SR Legacy April 2018
Both co-substrates are required; this is not a fixed dietary yield or an assertion that extra intake is rate-limiting.
Dependencies: Functional AGAT; glycine co-substrate availability; Tissue access and feedback regulation
Reaction identity does not prove dietary precursor limitation or cerebral delivery; SAM participation creates no independent methionine admission.
Dependencies: Functional GAMT; S-adenosylmethionine methyl supply; Interorgan exchange and receiving-tissue creatine transport
Arginine → Human AGAT transfers the amidino group of arginine to glycine, yielding guanidinoacetate and ornithine. → GAMT methylates guanidinoacetate using S-adenosylmethionine to form creatine. → Creatine
BRS4-FM1-PM3: Enable rapid ATP buffering so high-energy-demand tissues can meet sudden metabolic spikes.
Existing admission: Type A / derived; versioned-assessment. The complete derived relationship is admitted for this PM.
Capacity of the endogenous synthesis route is distinct from a claim that extra amino-acid intake raises cerebral creatine, phosphocreatine buffering or cognition. AGAT feedback, GAMT methyl supply, organ exchange and SLC6A8-mediated tissue transport constrain delivery. Human renal GAA production is not a measurement of brain synthesis flux; rat arginine infusion and glycine null responses are not oral human efficacy experiments.
- Lupin Beans — supplies Arginine; verified; raw. Lupins, mature seeds, raw
Composition provenance
USDA SR Legacy April 2018
- Watermelon — supplies Arginine; verified; raw. Watermelon, raw
Composition provenance
USDA SR Legacy April 2018
Both co-substrates are required; this is not a fixed dietary yield or an assertion that extra intake is rate-limiting.
Dependencies: Functional AGAT; glycine co-substrate availability; Tissue access and feedback regulation
Reaction identity does not prove dietary precursor limitation or cerebral delivery; SAM participation creates no independent methionine admission.
Dependencies: Functional GAMT; S-adenosylmethionine methyl supply; Interorgan exchange and receiving-tissue creatine transport
Glycine → Human AGAT transfers the amidino group of arginine to glycine, yielding guanidinoacetate and ornithine. → GAMT methylates guanidinoacetate using S-adenosylmethionine to form creatine. → Creatine
BRS4-FM1-PM3: Enable rapid ATP buffering so high-energy-demand tissues can meet sudden metabolic spikes.
Existing admission: Type A / derived; versioned-assessment. The complete derived relationship is admitted for this PM.
Capacity of the endogenous synthesis route is distinct from a claim that extra amino-acid intake raises cerebral creatine, phosphocreatine buffering or cognition. AGAT feedback, GAMT methyl supply, organ exchange and SLC6A8-mediated tissue transport constrain delivery. Human renal GAA production is not a measurement of brain synthesis flux; rat arginine infusion and glycine null responses are not oral human efficacy experiments.
Input identity/conversion is recorded; usable food-composition mapping remains unresolved.
Both co-substrates are required; this is not a fixed dietary yield or an assertion that extra intake is rate-limiting.
Dependencies: Functional AGAT; arginine co-substrate availability; Tissue access and feedback regulation
Reaction identity does not prove dietary precursor limitation or cerebral delivery; SAM participation creates no independent methionine admission.
Dependencies: Functional GAMT; S-adenosylmethionine methyl supply; Interorgan exchange and receiving-tissue creatine transport
Glycine → Human AGAT transfers the amidino group of arginine to glycine, yielding guanidinoacetate and ornithine. → GAMT methylates guanidinoacetate using S-adenosylmethionine to form creatine. → Creatine
BRS4-FM1-PM3: Enable rapid ATP buffering so high-energy-demand tissues can meet sudden metabolic spikes.
Existing admission: Type A / derived; versioned-assessment. The complete derived relationship is admitted for this PM.
Capacity of the endogenous synthesis route is distinct from a claim that extra amino-acid intake raises cerebral creatine, phosphocreatine buffering or cognition. AGAT feedback, GAMT methyl supply, organ exchange and SLC6A8-mediated tissue transport constrain delivery. Human renal GAA production is not a measurement of brain synthesis flux; rat arginine infusion and glycine null responses are not oral human efficacy experiments.
Input identity/conversion is recorded; usable food-composition mapping remains unresolved.
Both co-substrates are required; this is not a fixed dietary yield or an assertion that extra intake is rate-limiting.
Dependencies: Functional AGAT; arginine co-substrate availability; Tissue access and feedback regulation
Reaction identity does not prove dietary precursor limitation or cerebral delivery; SAM participation creates no independent methionine admission.
Dependencies: Functional GAMT; S-adenosylmethionine methyl supply; Interorgan exchange and receiving-tissue creatine transport