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Fo-Ti
Reynoutria multiflora (Polygonum multiflorum)
TL;DR
Fo-Ti (he shou wu) is a traditional tonic root sold for grey hair and longevity. Human efficacy evidence is essentially absent, while the liver-injury signal is not: multiple countries have issued warnings and there are dozens of published hepatotoxicity cases. The risk-benefit here does not favour use.
Ideal For
- Nobody, on current evidence — the documented liver risk is not offset by any controlled benefit
Avoid If
- You have any liver condition or raised liver enzymes
- You drink alcohol regularly
- You take other hepatotoxic medication
- You are pregnant or breastfeeding
Frequently Asked Questions
Overview
Fo-Ti is the root of Reynoutria multiflora, known in Chinese medicine as he shou wu and traditionally processed with black bean broth before use. Marketing leans on the legend of restored black hair; the pharmacology mostly points at stilbene glycosides and anthraquinones. What the modern literature actually contains is a substantial hepatotoxicity case series — idiosyncratic drug-induced liver injury with a hepatocellular pattern, documented in China, Korea, Japan, Australia and Europe, sometimes requiring transplant. Raw (unprocessed) root carries more anthraquinone and appears riskier, but processed preparations have also been implicated. There is no controlled human trial showing hair or longevity benefit that would offset this.
How It Works
- Stilbene glycoside (TSG) shows antioxidant activity in cell and rodent models
- Anthraquinone content contributes a laxative effect and is implicated in liver toxicity
- Proposed 5-alpha-reductase and hair-follicle effects rest on rodent and in-vitro work
- Idiosyncratic hepatotoxicity is not dose-predictable
Benefits & Outcomes
No linked outcomes yet. Research is ongoing.
Supporting Research9 studies
HLA-B*35:01 allele is a potential biomarker for predicting Polygonum multiflorum-induced liver injury in humans
Li C, Rao T, Chen X +2 more
This study aimed to identify the genetic basis of susceptibility to PM-drug-induced liver injury (PM-DILI) and to develop biological markers for predicting the risk of PM-DILI in humans.
Liver Damage Associated with Polygonum multiflorum Thunb.: A Systematic Review of Case Reports and Case Series
Lei X, Chen J, Ren J +7 more
Hepatocellular injury predominated among reported cases of liver damage associated with Polygonum multiflorum.
Single-nucleotide polymorphisms of HLA and Polygonum multiflorum-induced liver injury in the Han Chinese population
Yang WN, Pang LL, Zhou JY +2 more
We conducted a systematic study enrolling 382 participants from four independent hospitals, including 73 PM-DILI patients, 118 patients with other drug-induced liver injury (other-DILI) and 191 healthy controls.
Polygonum multiflorum-Induced Liver Injury: Clinical Characteristics, Risk Factors, Material Basis, Action Mechanism and Current Challenges
Wang Y, Wang L, Saxena R +6 more
Polygonum multiflorum liver injury is largely idiosyncratic and immune-mediated, with a strong association to the HLA-B*35:01 allele.
The hepatotoxicity of Polygonum multiflorum: the emerging role of the immune-mediated liver injury
Rao T, Liu YT, Zeng XC +2 more
However, most epidemiological and clinical evidence demonstrate that PM-DILI is immune-mediated idiosyncratic liver injury.
Drug-Induced Liver Injury: Twenty Five Cases of Acute Hepatitis Following Ingestion of Polygonum multiflorum Thunb
Jung KA, Min HJ, Yoo SS +7 more
Twenty-five patients developed acute hepatocellular hepatitis after ingesting Polygonum multiflorum, with a mean latency of about 30 days.
Overview of pharmacokinetics and liver toxicities of Radix Polygoni Multiflori
Li D, Yang M, Zuo Z
However, its safe and effective application in clinical practice could be hindered by its liver injury potential and lack of investigations on its hepatotoxicity mechanism.
Phytochemistry, pharmacology, toxicology and detoxification of Polygonum multiflorum Thunb.
Qian J, Feng C, Wu Z +2 more
While, PM also has some toxicity, its clinical drug safety has been concerned.
Hair growth promotion activity and its mechanism of Polygonum multiflorum
Li Y, Han M, Lin P +2 more
However, several crucial problems in its clinic usage and mechanisms are still unsolved or lack scientific evidences.
Safety Information
Potential Side Effects
Loose stools and abdominal cramping from anthraquinones. Most importantly, idiosyncratic drug-induced liver injury: jaundice, dark urine, fatigue and raised transaminases, occasionally severe.
Contraindications
Any existing liver disease, pregnancy, breastfeeding, children, concurrent hepatotoxic drugs, or heavy alcohol use.
Drug Interactions
- Any hepatotoxic drug (methotrexate, isoniazid, high-dose paracetamol) — additive liver risk
- Warfarin (anthraquinone effect on transit and reported bleeding cases)
Pregnancy & Breastfeeding
Pregnancy: likely_unsafe
Breastfeeding: likely_unsafe
Dosage Guidelines
Dosage Used in Studies
Consult healthcare provider
Best Time to Take
Not applicable — use is not recommended
Best Form
If used at all under practitioner supervision, processed root with baseline and follow-up liver enzymes
Bioavailability
Stilbene glycosides are absorbed and rapidly conjugated; anthraquinones act mainly in the gut
Dosing by Goal
| Goal | Dose | Notes |
|---|---|---|
| Historically 3-15 g/day of processed root as decoction | We do not recommend a dose; hepatotoxicity is idiosyncratic, not dose-dependent |
Forms Compared
Traditional black-bean processing; still implicated in liver injury cases
Higher anthraquinone content; greater reported risk
Concentrates the studied stilbene but not shown safe long term
Food & Timing
Not applicable
Medical Disclaimer
The information provided on this website is for educational and informational purposes only and is not intended as a substitute for professional medical advice, diagnosis, or treatment. Always seek the advice of your physician or other qualified health provider with any questions you may have regarding a medical condition or before starting any supplement regimen.
Individual results may vary. The statements on this website have not been evaluated by the Food and Drug Administration. Products and information are not intended to diagnose, treat, cure, or prevent any disease.