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In plain terms

In plain terms: L-Tyrosine shows early signals in human research but the evidence is limited -- small trials, surrogate endpoints, or not yet independently replicated. It is an emerging area, not yet a proven one.

L-Tyrosine

C Limited: small, mixed or unreplicated trials
Category Supplements
Evidence Small randomized and controlled trials under acute stress
Reviewed July 2026
PMIDs 38975711 · 17585971 · 10230711 · 26285023 · 39820592 · 29168741
The endpoint this grade is based on: Objectively measured functional outcome, Working memory and reaction measures during acute environmental or operational stress, on small short trials: positive during severe cold exposure and a military combat course, null during exercise in heat, and null on stress markers in the one recent trial. Not a daily supplement claim: the positive trials gave 2 g doses or 150 to 300 mg per kilogram, far above a typical capsule.

The evidence as the record states it

McAllister et al. (Stress, 2024; PMID 38975711): 80 young adults randomized to 2,000 mg L-tyrosine, 200 mg L-theanine or placebo before a virtual-reality active-shooter drill and cognitive challenge; neither amino acid changed salivary alpha-amylase, secretory IgA, heart rate or state anxiety, and the only tyrosine result was fewer missed responses on the Stroop task. Mahoney et al. (Physiol Behav, 2007; PMID 17585971): 19 volunteers, double-blind within-subject, 300 mg/kg tyrosine in food bars during two 90-minute cold-water immersions at about 10 degrees Celsius; cold impaired a match-to-sample memory measure and tyrosine restored correct responses; US Army laboratory, indexed as a controlled trial rather than a randomized one. Deijen et al. (Brain Res Bull, 1999; PMID 10230711): 21 cadets during a combat training course, five daily 2 g doses in a protein drink against a carbohydrate drink; memory and tracking performance better on tyrosine, no mood effect; the control was a calorie-matched carbohydrate drink, not a matched placebo. Null: Coull et al. (Med Sci Sports Exerc, 2016; PMID 26285023), 150 mg/kg before a load-carriage protocol in 40 degree heat, 8 participants, no cognitive benefit; Donnan et al. (PLoS One, 2025; PMID 39820592), 150 mg/kg in 8 soccer players during intermittent exercise in 32 degree heat, no effect on decision making, power or affect. Harm signal in older adults: van de Rest et al. (Nutrients, 2017; PMID 29168741), 17 adults aged 60 to 75 given 100, 150 or 200 mg/kg; working memory declined with higher doses, most in those with the largest plasma rise. Grade C: small, short trials on objective tests under acute stress, positive in cold and combat settings, null in heat, with a dose-dependent decline in older adults. A 2017 tyrosine and brain-stimulation paper by another group was retracted and is not cited.

PMID 38975711 PMID 17585971 PMID 10230711 PMID 26285023 PMID 39820592 PMID 29168741

Why Grade C and not Grade B

Grade C reflects early or limited human evidence -- small trials, surrogate endpoints, or preliminary findings not yet independently replicated. The evidence points in a promising direction but does not yet meet the standard for Grade B. A single well-powered, independently replicated trial with a meaningful endpoint would move this to Grade B or higher.

What this grade covers and what it does not

Grade C on working memory and reaction measures during acute stress. The evidence is small and short: 19 volunteers in severe cold (Mahoney et al., 2007; PMID 17585971), 21 cadets in combat training (Deijen et al., 1999; PMID 10230711) and 80 young adults in a simulated shooting drill where only one Stroop measure moved and stress markers did not (McAllister et al., 2024; PMID 38975711). Two heat-stress trials were null (Coull et al., 2016; PMID 26285023; Donnan et al., 2025; PMID 39820592). Objective tests, inconsistent results across settings: C. WHAT THIS GRADE DOES NOT COVER: stress markers such as cortisol, alpha-amylase or anxiety scores, which did not change; any daily supplement dose, since the trials gave 2 g or 150 to 300 mg/kg; exercise in heat, where the trials were null; and older adults, in whom higher doses worsened working memory (van de Rest et al., 2017; PMID 29168741).

What would move this grade

A well-powered randomized trial with an objective, clinically meaningful primary endpoint and at least one independent replication would support Grade B or higher.

How to track whether this is working The positive trials measured working memory and reaction tasks during an acute stressor; outside such a setting there is no measured outcome on this record. Thyroid function (TSH, T3, T4) at baseline and 12 weeks if used long term, as tyrosine is a thyroid hormone precursor.