Side-by-side comparison of mechanisms, dosing, interactions, and stacking potential.
| Alpha-GPC | Gotu Kola (Centella asiatica) | |
|---|---|---|
| Category | Nootropics | Nootropics |
| Standard Dose | 300-600 mg/day | 500-1000 mg/day of standardized extract (35-45% triterpenes) or 750-1500 mg/day of whole herb extract |
| Timing | Morning or pre-workout. Can be taken with or without food. Split into 1-2 doses. | Morning or split morning/afternoon. With or without food. Acute mood effects (alertness, reduced anger) noted within 1 hour of dosing. |
| Cycle Duration | Ongoing; no cycling required for standard doses | Ongoing; traditional use suggests no cycling required. Clinical trials run 2-6 months. |
| Evidence Level | strong_human | moderate_human |
Highly bioavailable choline source that crosses the blood-brain barrier efficiently via passive diffusion. Serves as a direct precursor for acetylcholine synthesis and phosphatidylcholine, a major structural component of neuronal membranes. Also stimulates growth hormone release via cholinergic activation of GHRH-releasing neurons in the hypothalamus. Contains ~40% choline by weight.
300-600 mg/day
Morning or pre-workout. Can be taken with or without food. Split into 1-2 doses.
Ongoing; no cycling required for standard doses
Pentacyclic triterpenes — asiaticoside, madecassoside, asiatic acid, and madecassic acid — provide neuroprotection through multiple mechanisms: inhibition of acetylcholinesterase activity and enhancement of cholinergic transmission; reduction of phospholipase A2 (PLA2) activity to attenuate neuroinflammation; protection against beta-amyloid aggregation and tau hyperphosphorylation; and upregulation of BDNF to promote neuronal growth and synaptic plasticity. Asiaticoside enhances collagen synthesis and wound healing, while asiatic acid activates the MAPK/ERK pathway to promote neurite outgrowth.
500-1000 mg/day of standardized extract (35-45% triterpenes) or 750-1500 mg/day of whole herb extract
Morning or split morning/afternoon. With or without food. Acute mood effects (alertness, reduced anger) noted within 1 hour of dosing.
Ongoing; traditional use suggests no cycling required. Clinical trials run 2-6 months.
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