Quick Comparison
| Glycine | L-Theanine | |
|---|---|---|
| Half-Life | 1-2 hours (plasma) | 2.5-4.5 hours |
| Typical Dosage | For sleep: 3 g taken 30-60 minutes before bed. For general nootropic use: 1-3 g daily. For NMDA co-agonism (with racetams): 1-3 g daily. Sweet taste, dissolves easily. | Standard: 100-200 mg daily. With caffeine: 100-200 mg L-Theanine per 50-100 mg caffeine (2:1 or 1:1 ratio). Can be taken up to 400 mg daily safely. |
| Administration | Oral (powder, capsules). Sweet-tasting powder dissolves easily in water. | Oral (capsules, powder, naturally in green tea). 100% bioavailable orally. |
| Research Papers | 10 papers | 10 papers |
| Categories |
Mechanism of Action
Glycine
Glycine acts as an inhibitory neurotransmitter by binding to strychnine-sensitive glycine receptors (GlyR) in the brainstem, spinal cord, and retina, hyperpolarizing neurons via chloride influx. It also serves as a mandatory co-agonist at the glycine-binding site (NR1 subunit) of NMDA glutamate receptors — without glycine binding, NMDA receptors cannot open their ion channel even when glutamate is present. This dual role means glycine both calms neural activity (sleep, anti-anxiety via GlyR) and supports excitatory learning processes (NMDA-dependent LTP and memory consolidation). Glycine lowers core body temperature at night by promoting peripheral vasodilation through nitric oxide, which improves sleep onset. It is a precursor for glutathione synthesis and modulates the glycinergic system in the suprachiasmatic nucleus.
L-Theanine
L-Theanine (gamma-glutamylethylamide) crosses the blood-brain barrier via the large neutral amino acid transporter (LAT1/SLC7A5) and exerts anxiolytic effects through multiple pathways. It increases GABA synthesis by serving as a substrate for glutamate decarboxylase (GAD), elevating inhibitory tone without directly binding GABA-A receptors — avoiding sedation. It modulates serotonin by increasing tryptophan hydroxylase (TPH2) activity and raises dopamine levels in the prefrontal cortex via inhibition of dopamine reuptake. L-Theanine antagonizes glutamate binding at AMPA and kainate receptor subtypes (GluA1-4, GluK1-5), reducing excitatory neurotransmission and excitotoxicity risk. This glutamate antagonism, combined with increased GABA, drives the characteristic increase in alpha brain wave power (8-14 Hz) in the posterior parietal and occipital cortex — the EEG signature of relaxed alertness. When co-administered with caffeine, L-theanine attenuates caffeine-induced increases in blood pressure and anxiety by modulating sympathetic nervous system activation through alpha-2 adrenergic receptor pathways, while caffeine's dopaminergic and adenosine-blocking effects on focus and attention are preserved.
Risks & Safety
Glycine
Common
Essentially none at standard doses. Sweet taste makes it easy to take.
Serious
None documented. One of the safest supplements available.
Rare
Nausea, soft stools at very high doses (>10 g).
L-Theanine
Common
Very few side effects at standard doses. Mild drowsiness in some individuals.
Serious
None documented. Extremely safe with decades of human consumption data.
Rare
Headache, dizziness, gastrointestinal discomfort.
Full Profiles
Glycine →
The simplest amino acid, yet one of the most important for brain function and sleep quality. Glycine is an inhibitory neurotransmitter (like GABA), a co-agonist at NMDA receptors (enhancing learning), and a critical building block for glutathione (the body's master antioxidant). Taking 3g before bed reliably improves sleep quality and next-day cognitive performance.
L-Theanine →
An amino acid found naturally in green tea that promotes calm focus without drowsiness. L-Theanine is one of the most popular and well-studied nootropics, famous for its synergy with caffeine — the combination provides clean, jitter-free focus that neither compound achieves alone. It crosses the blood-brain barrier and modulates alpha brain waves associated with relaxed attention.