Alpha-GPCvsCDP-Choline

Alpha-GPC (L-alpha-glycerylphosphorylcholine) is hydrolyzed by phospholipases in the gut and brain to release free choline, which is transported across the blood-brain barrier via the choline transporter (CHT1) and taken up by neurons for acetylcholine synthesis via choline acetyltransferase (ChAT). It is the most efficient oral choline source for raising brain acetylcholine levels due to high bioavailability and direct utilization. Alpha-GPC also provides glycerophosphate (glycerol-3-phosphate), which enters the Kennedy pathway and supports phosphatidylcholine and cell membrane phospholipid synthesis. It may stimulate growth hormone release through cholinergic activation of the pituitary. Alpha-GPC enhances high-affinity choline uptake and supports muscarinic (M1, M2) and nicotinic receptor function.

CDP-Choline is hydrolyzed by nucleotidases and phosphatases into choline and cytidine after oral ingestion. Choline enters the acetylcholine synthesis pathway via choline acetyltransferase. Cytidine is phosphorylated to CTP and converted to uridine monophosphate (UMP), which enters the Kennedy pathway and stimulates the synthesis of phosphatidylcholine via the enzyme CTP:phosphocholine cytidylyltransferase — phosphatidylcholine is a critical component of neuronal cell membranes and synaptic vesicles. This dual mechanism simultaneously boosts neurotransmitter production and repairs membrane damage from oxidative stress or ischemia. CDP-Choline also increases dopamine D2 receptor density in the striatum and enhances dopamine release. It may modulate glutamate excitotoxicity and support mitochondrial function.