Tian Nan Xing
StarArisaema erubescens (Wall.) Schott; Arisaema heterophyllum Blume; Arisaema amurense Maxim.
Traditionally used for
- Dizziness
- Cough & breathing
- Nerves & recovery
Cautions & contraindications
- Pregnancy
- Kidney conditions
- Seizure disorders
- Toxic — professional use only
☯ TCM Properties
Dries Dampness and Transforms Phlegm; Transforms Wind-Phlegm and Stops Spasms; Disperses Swelling and Dissipates Nodules
Traditional Chinese Uses
Tian Nan Xing (arisaema rhizome) is a warm, pungent herb that dries Dampness and transforms stubborn Phlegm — particularly cold-type Phlegm that has become lodged in the channels and orifices. Its most significant applications are for Wind-Phlegm patterns causing convulsions, stroke sequelae with paralysis, facial deviation, numbness, and dizziness. Applied externally, it treats snake bites and carbuncles. It is highly toxic in its raw form and must be properly processed before internal use, with bile processing (Dan Nan Xing) creating a cool-natured form for heat Phlegm patterns.
Western Herbalism Properties
Relationships
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Botanical Description
Tian Nan Xing is the dried corm-like rhizome of several closely related species of Arisaema (Araceae), chiefly A. erubescens, A. heterophyllum, and A. amurense, all perennial tuberous herbs native to East Asia. Each year a single false stem (actually a long fleshy petiole) emerges from the depressed-globose corm, bearing one or two compound leaves with 7-19 radiating lance-shaped leaflets resembling a partly-opened hand. The inflorescence is a typical aroid spadix enclosed in a hooded green or purple-striped spathe with a long whip-like tip, ripening into a dense head of bright orange-red berries. The fresh corm is intensely acrid and irritant due to needle-like calcium oxalate raphides and must be processed (boiled with ginger, alum, or bile) before therapeutic use; raw material is considered toxic.
Active Constituents
Calcium oxalate raphides
Inorganic biomineral crystal (needle-shaped idioblast raphide)Concentration: Approximately 89.5 percent of the mass of raphides purified from Arisaema erubescens tubers; the remainder is protein (about 7.4 percent) and polysaccharide (about 0.5 percent)
The defining toxic principle of the raw drug. Scanning electron microscopy of raphides from A. erubescens shows needles sharp at both ends, grooved along both sides and in part barbed, so they mechanically pierce mucosa and act as a delivery vehicle for the co-packaged proteins. In humans this produces the acrid burning, hypersalivation, oropharyngeal oedema and, at worst, airway obstruction that make the unprocessed rhizome unsafe to swallow.
Arisaema erubescens lectin
Plant lectin (glycan-binding protein), agglutinatingConcentration: Component of the roughly 7.4 percent protein fraction of purified raphides
Purified from A. erubescens tubers and shown to be pro-inflammatory in its own right, identifying the protein rather than the crystal alone as a driver of the acrid irritant reaction. In the molluscicidal assay the intact raphide was more active than isolated calcium oxalate, which was in turn more active than the isolated lectin, so crystal and protein act together rather than either alone accounting for toxicity.
Schaftoside
Flavone C-glycoside (apigenin 6-C-glucosyl-8-C-arabinoside)Concentration: Isolated from the ethanol extract of A. erubescens tubers by bioassay-guided fractionation; no pharmacopoeial content limit assigned
One of the two principal flavone C-glycosides of the tuber and a practical chemical marker for the drug, since it is not destroyed by the processing that removes the raphides. Nematocidal against Meloidogyne incognita with an LC50 of 114.66 micrograms per millilitre.
Isoschaftoside
Flavone C-glycoside (apigenin 6-C-arabinosyl-8-C-glucoside)Concentration: Co-isolated with schaftoside from A. erubescens tubers
The positional isomer of schaftoside and the second major flavone C-glycoside of the tuber, roughly three-fold weaker in the same nematocidal assay (LC50 323.09 micrograms per millilitre). Of interest as an authentication marker rather than as a therapeutic principle.
beta-Sitosterol and daucosterol
Phytosterol and its 3-O-glucosideConcentration: Reported from Arisaema amurense rhizome, one of the three pharmacopoeial source species; not quantified
Ubiquitous non-toxic sterols recovered alongside mannitol in phytochemical work on A. amurense. They carry none of the acrid activity and are cited here for completeness of the chemical profile, not as active principles.
⚠ Drug Interactions
Unprocessed (raw) Arisaema rhizome taken internally
This is a substitution hazard rather than a pharmacokinetic interaction, and it is the single most important safety fact about this drug. The raw rhizome carries intact calcium oxalate raphides that pierce oral, pharyngeal and oesophageal mucosa and release pro-inflammatory protein. A 60-year-old man who swallowed a raw Arisaema amurense rhizome as a herbal medicine developed oral pain, swelling and hypersalivation, lost the ability to speak, and required endotracheal intubation for airway protection. An analogous case in a 4-year-old who chewed Arisaema triphyllum root showed hypersalivation, pharyngeal congestion and uvular swelling within two hours. Reported human effects also include oral ulceration, oesophageal erosion and hypocalcaemia.
Clinical note: Never dispense raw Arisaema for internal use. Only the processed drug belongs in a decoction: Arisaematis Rhizoma Praeparatum (Zhi Tian Nan Xing, ginger juice plus alum) or Arisaema cum Bile (Dan Nan Xing, the bile-fermented product held as a separate record in this corpus). Raw material is reserved for external application. If a patient presents after ingesting raw material, treat as an airway emergency.
Arisaema cum Bile (Dan Nan Xing) supplied or substituted for Tian Nan Xing
This record is the rhizome drug Rhizoma Arisaematis and the ginger-and-alum processed form derived from it; the bile-processed drug Dan Nan Xing is held as a separate record in this corpus and is not described again here. What the bile step changes is substantial. The powdered rhizome is combined with ox, sheep or pig bile and fermented, and during fermentation conjugated bile acids are converted to free bile acids, so the finished drug carries a bile-acid profile the plain rhizome does not have at all: twelve bile acids have been quantified in it by UPLC-MS, with content varying markedly by producing region. Gas chromatography ion-mobility work identifies seventeen volatile organic compounds that distinguish fermentation stages, with Enterococcus and Staphylococcus implicated in producing them; reported optimal fermentation time differs between studies, 15 days by bile-acid chemometrics and 3 months by volatile profile. Pharmacologically the products diverge as well as chemically: the bile drug is the one with anticonvulsant evidence, reversing hot-water-bath-induced febrile seizures in rats at 2.8 g/kg orally with hippocampal neuron preservation, raised GABA-A receptor and lowered GRIA1 expression. Traditionally the bile form is cold rather than warm and is used for phlegm-heat and childhood convulsions, where the ginger-processed form is warm and drying.
Clinical note: Specify which processed form you intend on the prescription. Dan Nan Xing is not a stronger or safer Tian Nan Xing; it is a colder drug with a different indication and a bile-acid component absent from the plain rhizome. Do not extrapolate the febrile-seizure animal data to the ginger-processed drug.
CNS depressants (benzodiazepines, barbiturates, alcohol, sedating antihistamines)
Arisaema rhizome preparations are described in the pharmacological literature as sedative and anticonvulsant, and Arisaema cum Bile has demonstrated anticonvulsant and GABA-pathway effects in a rat febrile-seizure model. No human pharmacokinetic or pharmacodynamic interaction study exists, and the sedative effect has not been quantified in people, so additive CNS depression remains an inference from animal data rather than a documented event.
Clinical note: Reasonable to ask about sedative and anticonvulsant medication before prescribing, and to avoid initiating both at once, but do not overstate this: no case of clinically significant additive sedation has been published.
Nephrotoxic drugs (aminoglycosides, cisplatin, high-dose NSAIDs)
In rats, crude Arisaema erubescens caused vacuolar degeneration of renal tubular epithelium with raised IL-1 beta, TNF-alpha and malondialdehyde and depressed antioxidant enzymes, and untargeted metabolomics found 35 perturbed biomarkers in amino acid, glycerophospholipid and fatty acid pathways. Both traditional processing routes, ginger-plus-alum and bovine bile, attenuated these changes. Correctly processed drug should therefore carry little of this risk; the concern applies to underprocessed or adulterated material and is animal, not human, evidence.
Clinical note: Use only verified processed material, keep courses short, and avoid stacking with nephrotoxic drugs in patients with existing renal impairment. Renal injury from properly processed Arisaema has not been reported in humans.
Dosage
| Form | Amount | Frequency | Duration | Population | Notes |
|---|---|---|---|---|---|
| topical | Appropriate amount | — | — | — | ChP 2025. The raw drug is EXTERNAL only — 外用生品适量,研末以醋或酒调敷患处. The internal form is processed Zhi Tian Nan Xing; bile-processed Dan Nan Xing is a separate drug. Caution in pregnancy; raw internal use is hazardous. Corrected from a generic 6-15g decoction filler value generated from tcm_category. |
Dui Yao — Herb Pairs
The classical two-herb combinations this herb appears in, each with an action neither herb has alone.
Both expel wind-phlegm and stop spasms, together calming tetany and convulsions.
Tetanus. Both are toxic; the formula is traditionally also applied externally.
Core pair of a classical formula — Yu Zhen San, Wai Ke Zheng Zong (Chen Shigong, 1617)
Evidence Tier
Moderate evidence · 7 studiesRecorded studies by study design, strongest design at the top. This is a study-design tier only, not a GRADE rating: it does not weigh risk of bias, consistency or precision.
Systematic review / meta-analysis
0
Randomized controlled trial
0
Other clinical trial
0
Observational / case report
2
2 verified · 0 unverified
In vitro / animal
5
5 verified · 0 unverified
Show 5 studies
- Insight into Nephrotoxicity and Processing Mechanism of Arisaema erubescens (Wall.) Schott by Metabolomics and Network Analysis
- Revealing the optimal traditional processing methods and its protective effects against febrile seizures of Arisaema cum bile
- Purification of a Lectin from Arisaema erubescens (Wall.) Schott and Its Pro-Inflammatory Effects
- Main active constituents and mechanism of toxicity of raphides from Arisaema erubescens against Oncomelania hupensis
- Nematocidal Flavone-C-Glycosides against the Root-Knot Nematode (Meloidogyne incognita) from Arisaema erubescens Tubers
Other / unclassified
0
Verified: design read from PubMed for a DOI that resolves to the cited paper Unverified: taken from the study's recorded description
Clinical Studies
Oropharyngeal Airway Obstruction after the Accidental Ingestion of Arisaema Amurense
A 60-year-old man ingested a raw Arisaema amurense rhizome as a medicinal herb and developed oral pain and swelling that progressed to aphonia and hypersalivation; he required endotracheal intubation for airway protection and was managed with antihistamines and corticosteroids. The authors attribute the injury to calcium oxalate content and note that reported effects range from oral oedema through oesophageal erosion to hypocalcaemia. Human evidence, on one of the three species that supply this drug, that the unprocessed rhizome is dangerous by mouth.
Poisoning due to Arisaema triphyllum Ingestion
A 4-year-old presented two hours after chewing the root of an unidentified garden plant, later identified as Arisaema triphyllum, with excessive salivation, inability to speak, posterior pharyngeal congestion and uvular swelling. The authors attribute the picture to calcium oxalate crystals and note the range from minor oral oedema to lethal airway obstruction. A congener rather than a pharmacopoeial source species, included because it independently documents the raphide syndrome in a human.
Insight into Nephrotoxicity and Processing Mechanism of Arisaema erubescens (Wall.) Schott by Metabolomics and Network Analysis
Rat study comparing crude Arisaema erubescens with the two traditional processed products, Arisaematis Rhizoma Praeparatum (ginger juice and alum) and Arisaema cum Bile (bovine bile). Crude drug produced renal tubular vacuolar degeneration with raised IL-1 beta, TNF-alpha and malondialdehyde and reduced antioxidant enzymes; untargeted metabolomics identified 35 candidate biomarkers in amino acid, glycerophospholipid and fatty acid metabolism, and both processing methods attenuated the perturbation. This is the closest thing to experimental validation that processing detoxifies the drug, and it is animal-level.
Revealing the optimal traditional processing methods and its protective effects against febrile seizures of Arisaema cum bile
Concerns the bile-processed drug rather than this record's rhizome, and is cited to define the boundary between them. Gas chromatography ion-mobility spectrometry identified 17 volatile organic compounds separating fermentation stages, with three months proposed as the optimal time and Enterococcus and Staphylococcus as the likely producing organisms. Arisaema cum bile at 2.8 g/kg orally increased seizure latency and shortened seizure duration in hot-water-bath-induced febrile seizures in rats, preserved hippocampal neurons, raised GABA-A receptor and lowered GRIA1 expression, and shifted gut microbiota. No equivalent anticonvulsant evidence exists for the ginger-and-alum processed rhizome.
Purification of a Lectin from Arisaema erubescens (Wall.) Schott and Its Pro-Inflammatory Effects
Isolation and characterisation of a lectin from A. erubescens tubers, with demonstration of pro-inflammatory activity. Establishes that the acrid toxicity of the raw drug is not attributable to calcium oxalate crystals alone but also to protein packaged with them, which is why processing steps that denature protein reduce irritancy.
Main active constituents and mechanism of toxicity of raphides from Arisaema erubescens against Oncomelania hupensis
Raphides purified from A. erubescens tubers were 89.46 percent calcium oxalate, 7.4 percent protein and 0.48 percent polysaccharide, and were strongly molluscicidal against the schistosomiasis snail Oncomelania hupensis (48-hour LC50 70.95 mg/L, 72-hour LC50 44.25 mg/L). Potency ranked intact raphides above isolated calcium oxalate crystals above isolated lectin. Electron micrographs showed needles sharp at both ends, grooved on both sides and partly barbed. A molluscicide study, not a therapeutic one, but the best quantitative anatomy of the toxic principle.
Nematocidal Flavone-C-Glycosides against the Root-Knot Nematode (Meloidogyne incognita) from Arisaema erubescens Tubers
Bioassay-guided fractionation of an ethanol extract of A. erubescens tubers yielded schaftoside and isoschaftoside, with nematocidal LC50 values of 114.66 and 323.09 micrograms per millilitre against Meloidogyne incognita. Source of the identity and relative abundance of the tuber's flavone C-glycosides; no relevance to human dosing.
⚠ Safety & Contraindications
- Pregnancy
- Kidney conditions
- Seizure disorders
- Toxic — professional use only
Contraindications
Contraindicated in pregnancy. Not for use in dryness or in yin deficiency with heat.
Safety Warnings
- The raw rhizome is not taken internally; only processed forms are used.
- Handle the raw drug with care — it irritates skin.
⚠ Toxicity Information
Intense burning and swelling of the mouth and throat on contact with the raw drug, with salivation and possible airway obstruction; numbness of the tongue.
Historical Texts
Shen Nong Ben Cao Jing
Han dynasty, compiled c. 200 CEBen Cao Shi Yi (Chen Cangqi)
Tang dynasty, 739 CEKai Bao Ben Cao
Northern Song dynasty, 973-974 CEBen Cao Gang Mu (Li Shizhen)
Ming dynasty, 1596References
- Qi CY, Wang J, Wu X, He SR, Zhang Q, Wu JH, Zhao CB. Botanical, Traditional Use, Phytochemical, and Toxicological of Arisaematis rhizoma . Evidence-Based Complementary and Alternative Medicine (2021) [DOI]
- Ali H, Yaqoob U. Traditional uses, phytochemistry, pharmacology and toxicity of Arisaema (Areaceae): a review . Bulletin of the National Research Centre (2021) [DOI]
- Zhao Q, Shan G, Xu D, Gao H, Shi J, Ju C, Lin G, Zhang F, Jia T. Simultaneous Analysis of Twelve Bile Acids by UPLC-MS and Exploration of the Processing Mechanism of Bile Arisaema by Fermentation . Journal of Analytical Methods in Chemistry (2019) [DOI]
This information is for educational purposes only and is not intended to replace professional medical advice. Always consult a qualified healthcare provider before using any herbal remedy, especially if you are pregnant, nursing, or taking medications.
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