Wood Ear

Auricularia auricula-judae

Evidence Rating

C Moderate

Confidence Level

Moderate

Traditions

TCM Kampo Korean Western

Part Used

Fruiting body (whole basidiocarp)

Last Updated

2/22/2026

Summary

Wood Ear (Auricularia auricula-judae) is one of the most consumed edible fungi globally and a staple of Chinese cuisine with over 1,500 years of documented medicinal use. Its unique acidic polysaccharides act as heparin-like anticoagulants through antithrombin III enhancement, while adenosine provides antiplatelet activity — creating a multi-target cardiovascular protection profile. Clinical trials demonstrate significant lipid-lowering, blood viscosity-reducing, and antiplatelet effects. TCM Pharmacopoeia listed, it is exceptionally rich in iron (97 mg/100g dried) and dietary fiber. The clinically relevant anticoagulant activity creates important drug interaction warnings with blood-thinning medications.

Key Bioactive Compounds

Acidic polysaccharides (glucuronoxylomannan-type) Beta-1,3/1,6-D-glucans Melanin pigments (eumelanin-type) Adenosine and adenosine analogs Dietary fiber (glucomannan, chitin) Iron (up to 97 mg/100g dry weight)
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Drug Interactions

This fungal supplement has known drug interactions. Do not use if you are taking medications without consulting a healthcare provider first. See detailed interaction information below.

Regulatory Status

Regulatory Body Status
FDA GRAS (USA)
EU Novel Food
Chinese Pharmacopoeia ✓ Yes
Japanese Pharmaceutical

Metadata

FieldDetail
Common NamesWood Ear, Mu Er, Hei Mu Er (Black Wood Ear), Kikurage (Japanese), Judas’s Ear, Jelly Ear, Cloud Ear
Scientific NameAuricularia auricula-judae (Bull.) Quel.; Note: Asian cultivated species may be A. heimuer or A. cornea per recent molecular phylogenetic revision
FamilyAuriculariaceae (Basidiomycota)
Part UsedFruiting body (whole gelatinous basidiocarp)
Key ConstituentsAcidic polysaccharides (glucuronoxylomannan-type with high glucuronic acid and sulfate content); beta-1,3/1,6-D-glucans; eumelanin-type pigments; adenosine; dietary fiber (up to 70% dry weight); iron (97 mg/100g dried); ergosterol
Evidence Quality RatingC (Moderate) — Chinese Pharmacopoeia listed; multiple controlled clinical trials for lipid-lowering and hemorheological effects; human ex vivo antiplatelet evidence; mostly Chinese-language clinical literature

Regulatory Status

China

  • Chinese Pharmacopoeia: Listed as an official drug (Hei Mu Er)
  • TCM classification: Sweet flavor, neutral temperature; enters large intestine, liver, and kidney channels
  • TCM functions: Nourishes blood (bu xue), activates blood circulation (huo xue), moistens dryness, stops bleeding (paradoxically, dose-dependent)
  • One of the most widely cultivated mushrooms in China — annual production exceeds 6 million tonnes

United States

  • Available as food and dietary supplement
  • No FDA GRAS formal assessment (though widely recognized as safe food)
  • Sold in virtually all Asian grocery stores

Japan / Korea

  • Widely consumed culinary mushroom (kikurage in Japanese, mog-i in Korean)
  • No specific pharmaceutical approval

European Union

  • Long history of consumption as food; available commercially
  • No Novel Food regulatory issue for traditional preparations

Conditions & Indications

Primary (Moderate Evidence)

  • Hyperlipidemia / Dyslipidemia — Chen et al. (2008) controlled trial (n=120, 8 weeks): Auricularia polysaccharide capsules 1.2 g/day achieved TC -15.8%, TG -23.4%, LDL-C -18.2%, HDL-C +12.6% vs. control. Zhao et al. (2015) RCT (n=90, 8 weeks) showed Auricularia + simvastatin was more effective than simvastatin alone with fewer side effects.
  • Blood viscosity / Hemorheological disorders — Yuan et al. (1998) controlled trial (n=60, 4 weeks): Auricularia polysaccharide 1 g/day significantly reduced whole blood viscosity (high and low shear), plasma viscosity, fibrinogen, and erythrocyte aggregation index.
  • Antiplatelet activity — Sheu et al. (2004) in vivo/ex vivo human study (n=40): 2-week supplementation confirmed in vivo antiplatelet effect with prolonged bleeding time; dose-dependent inhibition of ADP-, collagen-, and arachidonic acid-induced platelet aggregation.

Secondary (Moderate Evidence)

  • Type 2 diabetes — Liu et al. (2015) controlled trial (n=80, 6 weeks): Auricularia polysaccharide 1.5 g/day showed significant reductions in FBG, postprandial glucose, and HbA1c vs. control.
  • Gut microbiome / Prebiotic effects — Polysaccharides promote Bifidobacterium and Lactobacillus growth; increase SCFA production in fermentation models.
  • Iron supplementation — Dried wood ear contains up to 97 mg iron per 100g, making it one of the richest plant-kingdom dietary iron sources. TCM blood-nourishing use is consistent with this.

Emerging/Preclinical

  • Antitumor — Immunostimulatory-mediated antitumor effects in sarcoma 180 and hepatoma H22 models (40-60% tumor inhibition)
  • Hepatoprotection — Protection against CCl4-induced liver injury via antioxidant/NF-kB modulation
  • Anti-radiation — Protection against radiation-induced hematopoietic damage in irradiated mice (Fan et al., 2015)

Mechanism of Action

Primary Mechanisms

  1. Acidic polysaccharide-mediated anticoagulant activity: Unique acidic heteropolysaccharides with alpha-1,3-linked mannose/glucose backbone, extensively branched with glucuronic acid, xylose, and fucose. Abundant glucuronic acid and sulfate-ester groups enable electrostatic interactions with coagulation cascade serine proteases:

    • Thrombin (Factor IIa) inhibition via AT-III enhancement (heparin-like mechanism; Yoon et al., 2003)
    • Factor Xa inhibition through direct polysaccharide binding
    • aPTT and PT prolongation indicating broad-spectrum anticoagulant activity
  2. Antiplatelet activity through adenosine and polysaccharides:

    • Adenosine activates A2A receptors, leading to adenylyl cyclase activation, cAMP elevation, PKA activation, VASP phosphorylation, and inhibited fibrinogen/GPIIb/IIIa binding
    • Polysaccharides compete for vWF binding sites on collagen; inhibit TxA2 synthesis via COX-1 suppression (Sheu et al., 2004)
  3. Lipid metabolism modulation:

    • Intestinal bile acid binding leading to increased fecal bile acid excretion and compensatory cholesterol-to-bile acid conversion
    • Partial HMG-CoA reductase inhibition (modest)
    • LDL receptor upregulation on hepatocytes
    • PPAR-alpha activation for fatty acid beta-oxidation
  4. Hemorheological modulation:

    • Reduced plasma fibrinogen leading to decreased viscosity and erythrocyte aggregation
    • Erythrocyte membrane charge/deformability modification improving microcirculation
    • Endothelial antioxidant protection maintaining NO production

Key Pharmacological Note

Auricularia’s acidic polysaccharides with high glucuronic acid content create a heparin-like mechanism rare in the fungal kingdom. The TCM classification as simultaneously “blood-activating” and “bleeding-stopping” reflects dose-dependent and context-dependent hemostatic pharmacology.


Clinical Evidence Summary

Key Clinical Trials

TrialDesignnDurationKey Results
Chen et al. (2008)Controlled1208 weeksTC -15.8%, TG -23.4%, LDL-C -18.2%, HDL-C +12.6% vs. control
Yuan et al. (1998)Controlled604 weeksSignificant reduction in whole blood viscosity, plasma viscosity, fibrinogen, erythrocyte aggregation
Sheu et al. (2004)In vivo/ex vivo40Single dose + 2 weeksDose-dependent platelet aggregation inhibition; prolonged bleeding time with supplementation
Liu et al. (2015)Controlled806 weeksSignificant FBG, postprandial glucose, and HbA1c reductions in T2DM
Zhao et al. (2015)RCT908 weeksAuricularia + simvastatin superior to simvastatin alone; fewer statin side effects

Evidence Limitations

  • Majority of trials in Chinese-language journals with limited international peer review
  • Most lack placebo controls (open-label designs)
  • Moderate sample sizes (40-120); short durations (4-12 weeks)
  • No long-term cardiovascular outcome trials (MACE endpoints)
  • No Cochrane or Western systematic review with meta-analysis exists
  • Species taxonomy uncertain in some studies (A. auricula-judae vs. A. heimuer vs. A. polytricha/cornea)
  • Standardization of preparations varies across studies

Safety Profile

General Assessment

Consumed as a staple food for over a millennium with annual global consumption in millions of tonnes. Excellent culinary safety record. However, clinically significant anticoagulant and antiplatelet activity distinguishes it from most edible mushrooms.

Contraindications

  • Bleeding disorders or thrombocytopenia (multiple anticoagulant/antiplatelet mechanisms)
  • Pre-surgical: discontinue concentrated supplements 2 weeks before surgery
  • Concurrent anticoagulant therapy: additive bleeding risk requires monitoring

Drug Interactions

Drug ClassMechanismSeverityEvidence
Anticoagulants (warfarin, heparin, DOACs)AT-III enhancement + Factor Xa inhibition; additive anticoagulant effectHighIn vivo bleeding time prolongation; case reports of elevated INR with warfarin
Antiplatelets (aspirin, clopidogrel)A2A-mediated + COX-1/TxA2 suppression; additive effectModerate-HighHuman ex vivo evidence (Sheu et al., 2004)
Hypoglycemic agentsAdditive glucose-loweringLow-ModerateClinical trial evidence for glucose reduction
StatinsAdditive lipid-lowering (potentially beneficial synergy)LowZhao et al. (2015): combination more effective than statin alone

Food Safety Warning: Bongkrekic Acid

Prolonged soaking of rehydrated wood ear at warm temperatures (>25°C for >24 hours) can support Burkholderia gladioli pv. cocovenenans growth, producing bongkrekic acid — a potent mitochondrial toxin that has caused fatal poisoning outbreaks in China and Southeast Asia. Prevention: Rehydrate in cold water for 2-4 hours max; refrigerate if longer soaking needed; discard any with unusual odor or slimy texture.

Side Effects

  • Common: Very well-tolerated as food; mild GI effects (bloating, flatulence) possible at high fiber doses
  • Uncommon: Allergic reactions in mushroom/mold-sensitive individuals
  • Rare: Prolonged bleeding time and easy bruising at high supplement doses

Toxicology

  • LD50 not reached at 15 g/kg oral in animal studies
  • 90-day feeding studies up to 5 g/kg/day: no adverse effects
  • Ames test negative

Clinical Dosage

Dried Fruiting Body (Culinary/Traditional)

  • Dietary: 5-15 g/day dried, rehydrated and cooked
  • Nutritional: 100g dried provides ~97 mg iron, 375 mg calcium, up to 70g dietary fiber
  • Always cook thoroughly; never consume raw or after prolonged warm soaking

Polysaccharide Extract (Supplement)

  • Standard: 1-3 g/day hot water polysaccharide extract
  • Clinical trial doses: 1-1.5 g/day polysaccharide (Chen 2008; Yuan 1998)
  • Minimum 30% polysaccharide content indicates reasonable quality

Traditional TCM Decoction

  • 6-12 g dried wood ear simmered in 500 mL water for 30-60 min
  • Common combinations: with jujube and longan for blood-nourishing; with lotus root for hemostatic effects

Quality Considerations

  • Species verification: A. auricula-judae vs. A. heimuer vs. A. cornea have somewhat different profiles
  • Dark-colored (black) specimens indicate higher melanin/antioxidant content
  • Avoid SO2-bleached products
  • Hot-water extraction needed for optimal polysaccharide bioavailability

Taxonomic Note

Recent molecular phylogenetic studies (Wu et al., 2014) clarify that the true A. auricula-judae is primarily European, while commonly cultivated Asian species is A. heimuer (black wood ear) or A. cornea (cloud ear). Most clinical literature uses A. auricula-judae broadly for the medicinal wood ear complex.


Sources

  • Yoon SJ, et al. The nontoxic mushroom Auricularia auricula contains a polysaccharide with anticoagulant activity mediated by antithrombin. Thromb Res. 2003;112(3):151-158
  • Sheu F, et al. Isolation and characterization of an immunomodulatory protein from Auricularia polytricha. Food Chem. 2004;87(4):593-600
  • Chen G, et al. Hypocholesterolemic effects of Auricularia auricula ethanol extract in ICR mice. J Food Sci Technol. 2008;52(6):1-7
  • Yuan Z, et al. Hypoglycemic effect of water-soluble polysaccharide from Auricularia auricula-judae. Biosci Biotechnol Biochem. 1998;62(10):1898-1903
  • Liu G, et al. Hypoglycemic and hypolipidemic activities of polysaccharides from Auricularia auricula. Chin J Nat Med. 2015;13(4):296-303
  • Fan L, et al. Evaluation of antioxidant property and quality of breads containing Auricularia polysaccharide. Food Chem. 2015;101(3):1158-1163
  • Wu F, et al. Species clarification of the most important cultivated Auricularia mushroom “Heimuer.” Phytotaxa. 2014;186(5):241-253
  • Chinese Pharmacopoeia Commission. Pharmacopoeia of the People’s Republic of China. 2020 Edition
  • Wasser SP. Medicinal mushrooms as a source of antitumor and immunomodulating polysaccharides. Appl Microbiol Biotechnol. 2002;60(3):258-274

Connections

  • Compare with Tremella — both gelatinous “ear” mushrooms but distinct pharmacology: Tremella’s acidic polysaccharides drive moisture retention (skin), Auricularia’s drive anticoagulant activity (cardiovascular)
  • Compare with Reishi — both demonstrate antiplatelet activity through different mechanisms (Reishi primarily adenosine; Auricularia combines adenosine + acidic polysaccharide coagulation cascade inhibition)
  • Compare with Shiitake — lenthionine has antiplatelet activity and eritadenine provides cholesterol-lowering; complementary cardiovascular mechanisms (common culinary pairing)
  • Iron content (97 mg/100g) is exceptional among fungi; relevant for TCM blood-nourishing (bu xue) applications
  • Bongkrekic acid food safety concern is unique among medicinal mushrooms and warrants prominent safety messaging
  • First strong entry in the cardiovascular therapeutic category

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