Berberine

72
evidence score
supplement
318 studies
berberine HClberberine hydrochlorideberberine chloride

Berberine is an isoquinoline alkaloid found in plants including Berberis and goldenseal. Extensive clinical trial data (primarily from China) demonstrates efficacy comparable to metformin for type 2 diabetes blood glucose control. Activates AMPK — the primary cellular energy sensor — driving downstream effects on glucose metabolism, lipid metabolism, and inflammation. Also improves lipid profiles (LDL-C reduction comparable to low-dose statins in some studies). Increasingly recognized as a legitimate metabolic therapeutic. Used for blood glucose management, weight loss, PCOS, and cardiovascular risk reduction. Bioavailability is poor (5–20%) but active, and can be improved with lipid formulations. Generally well-tolerated.

Evidence

Moderate evidence

Safety

Unknown safety profile

Clinical Status

Phase II

Research Sync

Feb 19, 2026

Dosing

Typical
1000 mg
500 mgRange1500 mg
Frequency500mg 2–3x daily with meals

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Pharmacology

Half-life~4–6 hours
OnsetBlood glucose effects within days; lipid effects over 4–8 weeks
DurationEffects active during dosing; benefits may partially persist
Routes
oral

Evidence Score

72
Level BModerate
318 studies indexed · 6 meta-analyses
Scoring Factors
Volume(40%)~50/100
Quality(30%)~48/100
Sample Size(10%)~100/100
Consistency(10%)~100/100
Replication(5%)~100/100
Recency(5%)~100/100

Scores estimated from study counts. Exact breakdown computed after research sync.

Evidence Levels
AScore ≥75 with at least 1 meta-analysis and 3+ RCTs
BScore ≥50 with at least 1 RCT or meta-analysis
CScore ≥25 — observational or animal evidence only
DScore <25 — very limited or preclinical data

Plain-English Snapshot

Berberine is currently categorized as a supplement compound.

Evidence is moderate (72/100): promising signal from 318 indexed studies, but context and population still matter.

Safety scoring is incomplete. Start conservatively and monitor carefully.

Core mechanism

AMPK activator; inhibits complex I of mitochondrial respiratory chain (similar to metformin); reduces hepatic gluconeogenesis; activates GLUT4 translocation; reduces intestinal glucose absorption

Practical Context

Strongest current signals

  • Level A: The effect of berberine on obesity indices: a systematic review and meta-analysis.
  • Level A: Gegen Qinlian decoction ameliorates insulin resistance in type 2 diabetes: A systematic review and meta-analysis of RCTs with mechanistic insights into SIRT1/AMPK pathway activation.
  • Level B: The Pharmacokinetic Interaction Between Metformin and the Natural Product Goldenseal Is Metformin Dose-Dependent: A Three-Arm Crossover Study in Adults With Type 2 Diabetes.

Compound Profile