Resveratrol
Resveratrol (trans-Resveratrol)
Evidence & Status
- Preliminary / Experimental
- Preliminary
At a Glance
Purified trans-resveratrol has limited short-term human metabolic research; it has not been shown to extend human lifespan.
Plain English
Resveratrol is a plant compound, but purified trans-resveratrol is not the same thing as drinking wine, eating grapes, using Japanese knotweed extracts, or taking pterostilbene. One cited human study was small and lasted only 30 days, so it cannot answer whether resveratrol prevents disease or extends lifespan. The body absorbs resveratrol but rapidly changes most of it into metabolites, leaving very little unchanged compound in circulation. Its connection with SIRT1 remains an active mechanistic question rather than a settled explanation for a longevity benefit.
Overview
This record is limited to purified trans-resveratrol and does not equate it with cis-resveratrol, pterostilbene, grape or wine consumption, Japanese knotweed extracts, or multi-ingredient supplements. In a randomized double-blind crossover study of 11 obese men, 150 mg/day resveratrol was evaluated for 30 days for short-term metabolic and mitochondrial outcomes. This small, short study does not establish disease prevention, calorie-restriction equivalence, or human longevity benefit. A human pharmacokinetic study found high absorption but very low oral bioavailability of unchanged resveratrol because of extensive metabolism. Resveratrol has been linked to SIRT1-related signaling, but direct SIRT1 activation is substrate- and assay-dependent and remains mechanistically debated. Resveratrol is marketed as a dietary-supplement ingredient, not an FDA-approved treatment represented by this record.
Research Summary
The cited human intervention was a randomized double-blind crossover study in 11 obese men using 150 mg/day for 30 days. It provides short-term metabolic and mitochondrial context only; it does not show disease prevention, calorie-restriction equivalence, or human longevity benefit. A separate human pharmacokinetic study found high absorption but very low oral bioavailability of unchanged resveratrol due to extensive metabolism. Resveratrol has been linked to SIRT1-related signaling, but direct activation claims were challenged with native substrates and remain substrate- and assay-dependent. Animal and pathway findings do not establish human lifespan extension.
Research Areas
- Longevity
- Sirtuin pathway
- Cardiovascular health
- Metabolic health
- Antioxidant
- Inflammation
- Neuroprotection
Safety & Risks
Serious Risks
- The cited human metabolic study was small and short-term; it does not establish disease prevention or human longevity benefit
- High absorption does not establish high systemic exposure to unchanged resveratrol; the cited human pharmacokinetic study found very low oral bioavailability of unchanged resveratrol
- Direct SIRT1 activation is substrate- and assay-dependent and remains mechanistically debated
- Human lifespan extension has not been established
Reported Side Effects
- The evidence represented here does not establish broad long-term safety across doses, formulations, or populations
- Human safety and interaction evidence varies by formulation, dose, co-medications, and population
Legal Status by Region
- United States
- Marketed as a dietary-supplement ingredient; not an FDA-approved treatment represented by this record.
- United Kingdom
- Jurisdiction-specific status is not assessed in this reference.
- Australia
- Jurisdiction-specific status is not assessed in this reference.
- Canada
- Jurisdiction-specific status is not assessed in this reference.
Citations & Sources
- Calorie restriction-like effects of 30 days of resveratrol supplementation on energy metabolism and metabolic profile in obese humans.
Cell Metabolism · 2011
PMID 22055504 · DOI 10.1016/j.cmet.2011.10.002
- High absorption but very low bioavailability of oral resveratrol in humans.
Drug Metabolism and Disposition · 2004
PMID 15333514 · DOI 10.1124/dmd.104.000885
- SRT1720, SRT2183, SRT1460, and resveratrol are not direct activators of SIRT1.
The Journal of Biological Chemistry · 2010
PMID 20061378 · DOI 10.1074/jbc.M109.088682