ALCARvsHoly Basil (Tulsi)

ALCAR crosses the blood-brain barrier via the organic cation transporter (OCTN2) more effectively than L-carnitine. In neurons, it is hydrolyzed by carnitine acetyltransferase to donate its acetyl group to coenzyme A, forming acetyl-CoA—which can then be used for acetylcholine synthesis via choline acetyltransferase, effectively providing raw material for the memory neurotransmitter. ALCAR also transports long-chain fatty acids across the inner mitochondrial membrane via the carnitine palmitoyltransferase system for beta-oxidation and ATP production. ALCAR activates nerve growth factor (NGF) signaling, possibly through modulation of NGF receptor (TrkA) expression or downstream MAPK/ERK pathways. It has antioxidant properties, reducing lipid peroxidation in mitochondrial membranes and scavenging free radicals. These mechanisms support cognitive function and neuroprotection.

Holy basil's adaptogenic effects come from multiple compounds: eugenol (anti-inflammatory via COX-2 and 5-LOX inhibition, TRPV1 modulation), ursolic acid (cortisol modulation via 11beta-HSD inhibition and glucocorticoid receptor modulation), rosmarinic acid (antioxidant via Nrf2/ARE pathway, anti-allergic via mast cell stabilization), and ocimumosides A and B (anti-stress via CRH and corticosterone reduction). It modulates the HPA axis, normalizing cortisol and corticosterone levels through hypothalamic and adrenal effects. Ursolic acid inhibits acetylcholinesterase (AChE), mildly increasing synaptic acetylcholine. Eugenol provides direct anxiolytic effects through GABA-A receptor positive allosteric modulation (possibly at the beta2/3 subunit interface) and 5-HT1A partial agonism. Ocimumosides may reduce ACTH release from the pituitary.