Botanical species · safety record

Xanthium strumarium

The EFSA Compendium of Botanicals holds 5 constituent measurements, 27 adverse-effect records and 3 genotoxicity assays for Xanthium strumarium. This page reports what those source records contain and how to reach them. It carries no effect estimate, no dose and no recommendation.

Accepted name in source: Xanthium strumarium L.

5Constituent measurements
30Safety records
12Cited sources
0Licensed products (Canada)

Regulatory presence

No Health Canada licensed natural health product in the snapshot names this species as a medicinal ingredient under this exact binomial. Absence here means absence from this one register under this one name, not absence from trade, and not a safety verdict.

What the records describe

Constituents measured

  • Sesquiterpene lactones2
  • 3,4-dihydroxybenzoic acid1
  • Atractyloside1
  • Cyanogenic glycosides1

Plant parts

  • Seed10
  • Sprout7
  • Aerial part of plants6
  • Live plants4
  • Fruit unspecified3
  • Leaves2

Preparations

  • Solvent extraction16

Effect types

  • Hepatotoxicity12
  • Neurotoxicity6
  • Nephrotoxicity4
  • Other toxicities3
  • Digestive1
  • None1

Target tissues

  • Liver12
  • Neurologic8
  • Urogenital: kidneys4
  • Digestive3

Recorded constituents

What analytical work has found in this species, at which plant part and preparation. A measured constituent is a fact about material, not about effect.

SubstancePlant partPreparationConcentrationAnalytical methodSource
3,4-dihydroxybenzoic acidFruit unspecifiedSolvent extraction—Nuclear Magnetic Resonance (NMR)Resolve DOI
Sesquiterpene lactonesLeavesSolvent extraction—Nuclear Magnetic Resonance (NMR)Resolve DOI
Sesquiterpene lactonesLeavesSolvent extraction—Nuclear Magnetic Resonance (NMR)Resolve DOI
AtractylosideFruit unspecifiedSolvent extraction—GC-MSNo resolvable identifier
Cyanogenic glycosidesSeed———No resolvable identifier

Recorded adverse effects

Adverse effects reported in the source literature, most often in animal or laboratory models at a stated preparation and dose.

EffectTarget tissuePlant partPreparationTest organismTest typeSource
DigestiveDigestiveSeed—Human (as organism)Case reportResolve DOI
HepatotoxicityLiverSeed—Human (as organism)Case reportResolve DOI
HepatotoxicityLiverSeed—Cattle (as animal)Case reportResolve DOI
HepatotoxicityLiverSprout—Cattle (as animal)Case reportResolve DOI
NephrotoxicityUrogenital: kidneysSeed—Human (as organism)Case reportResolve DOI
NeurotoxicityNeurologicSeed—Human (as organism)Case reportResolve DOI
NeurotoxicityNeurologicSeed—Cattle (as animal)Case reportResolve DOI
NeurotoxicityNeurologicSprout—Cattle (as animal)Case reportResolve DOI
Other toxicitiesDigestiveFruit unspecifiedSolvent extraction—In vitroResolve DOI
HepatotoxicityLiverLive plantsSolvent extractionHuman (as organism)Case reportNo resolvable identifier
HepatotoxicityLiverLive plantsSolvent extractionHuman (as organism)Case reportNo resolvable identifier
HepatotoxicityLiverSprout—Pig (as animal)Short-term toxicityNo resolvable identifier
HepatotoxicityLiverSprout—Pig (as animal)OtherNo resolvable identifier
HepatotoxicityLiverSeed—Pig (as animal)SubchronicNo resolvable identifier
HepatotoxicityLiverSprout—Pig (as animal)OtherNo resolvable identifier
HepatotoxicityLiverSeed—Pig (as animal)SubchronicNo resolvable identifier
HepatotoxicityLiverAerial part of plantsSolvent extractionRat (as animal)Short-term toxicityNo resolvable identifier
HepatotoxicityLiverAerial part of plantsSolvent extractionRat (as animal)Short-term toxicityNo resolvable identifier
NephrotoxicityUrogenital: kidneysSprout—Pig (as animal)Short-term toxicityNo resolvable identifier
NephrotoxicityUrogenital: kidneysAerial part of plantsSolvent extractionRat (as animal)Short-term toxicityNo resolvable identifier
NephrotoxicityUrogenital: kidneysAerial part of plantsSolvent extractionRat (as animal)Short-term toxicityNo resolvable identifier
NeurotoxicityNeurologicSprout—Pig (as animal)Short-term toxicityNo resolvable identifier
NeurotoxicityNeurologicLive plantsSolvent extractionHuman (as organism)Case reportNo resolvable identifier
NeurotoxicityNeurologicLive plantsSolvent extractionHuman (as organism)Case reportNo resolvable identifier
NoneDigestiveSeedSolvent extractionHuman (as organism)In vitroNo resolvable identifier
Other toxicitiesNeurologicAerial part of plantsSolvent extractionRat (as animal)Short-term toxicityNo resolvable identifier
Other toxicitiesNeurologicAerial part of plantsSolvent extractionRat (as animal)Short-term toxicityNo resolvable identifier

Genotoxicity testing

Outcomes of genotoxicity assays as recorded in the source. A negative assay is a result under those test conditions, not a clearance.

OutcomeEndpointTestTested organismMetabolic activationSource
PositiveDNA damage and/or repairsingle cell gel/comet assay in mammalian cells for detection of DNA damageRat (as animal)WithoutResolve DOI
Positivechromosome aberrationsister chromatid exchange assay in mammalian cellsRat (as animal)WithoutResolve DOI
Positivechromosome aberrationchromosome aberration assayRat (as animal)WithoutResolve DOI

Cited sources

The literature the compendium cites for this species. Metatron Health has no relationship with these authors or journals and earns nothing from citing them.

  1. Botha, Christo J., Lessing, Dries., Roesemann, Magda., van Wilpe, Erna., Williams, June H. Analytical confirmation of Xanthium strumarium poisoning in cattle. Journal of veterinary diagnostic investigation, 2014, vol. 26, no. 5, p. 640-645. DOI
  2. Hwang, Seung Hwan., Wang, Zhiqiang., Yoon, Ha Na., Lim, Soon Sung. Xanthium strumarium as an Inhibitor of alpha-Glucosidase, Protein Tyrosine Phosphatase 1beta, Protein Glycation and ABTS(+) for Diabetic and Its Complication. . Molecules (basel, switzerland), 2016, vol. 21, no. 9. DOI
  3. Islam, Mohammad Rashedul., Uddin, Mohammad Zashim., Rahman, Mohammad Sharifur., Tutul, Ershad., Rahman, Mohammed Zakiur., Hassan, Md Abul., Faiz, M A., Hossain, Moazzem., Hussain, Maleeha., Rashid, Mohammad Abdur. Ethnobotanical, phytochemical and toxicological studies of Xanthium strumarium L. . Bangladesh medical research council bulletin, 2009, vol. 35, no. 3, p. 84-90.
  4. Masvingwe, C., Mavenyengwa, M. Toxicological evaluation of the plant Xanthium strumarium in pigs in Zimbabwe . Journal of venomous animals and toxins, 1998, vol. 4, no. 2 CITED APRIL 18, 2000, p. 1-8.
  5. Piloto Ferrer, Janet., Cozzi, Renata., Cornetta, Tommaso., Stano, Pasquale., Fiore, Mario., Degrassi, Francesca., De Salvia, Rosella., Remigio, Antonia., Francisco, Marbelis., Quinones, Olga., Valdivia, Dayana., Gonzalez, Maria L., Perez, Carlos., Sanchez-Lamar, Angel. Xanthium strumarium L. extracts produce DNA damage mediated by cytotoxicity in in vitro assays but does not induce micronucleus in mice. . Biomed research international, 2014, vol. 2014, p. 575197-575197. DOI
  6. STUART, BP., COLE, RJ., GOSSER, HS. COCKLEBUR (XANTHIUM-STRUMARIUM, L VAR STRUMARIUM) INTOXICATION IN SWINE - REVIEW AND REDEFINITION OF THE TOXIC PRINCIPLE . Veterinary pathology, 1981, vol. 18, no. 3, p. 368-383.
  7. Saidi, Hossein., Mofidi, Mani. TOXIC EFFECT OF XANTHIUM STRUMARIUM AS AN HERBAL MEDICINE PREPARATION. Excli journal, 2009, vol. 8, p. 115-117.
  8. Turgut, M., Alhan, CC., Gurgoze, M., Kurt, A., Dogan, Y., Tekatli, M., Akpolat, N., Aygun, D. Carboxyatractyloside poisoning in humans. Annals of tropical paediatrics, 2005, vol. 25, no. 2, p. 125-134. DOI
  9. ESASHI, Y., MATSUYAMA, S., ASHINO, H., OGASAWARA, M., HASEGAWA, R. BETA-GLUCOSIDASE ACTIVITIES AND HCN LIBERATION IN UNIMBIBED AND IMBIBED SEEDS, AND THE INDUCTION OF COCKLEBUR SEED-GERMINATION BY CYANOGENIC GLYCOSIDES . Physiologia plantarum, 1991, vol. 83, no. 1, p. 34-40.
  10. Chu, Chien-Hua., Chiu, Chi-Ming., Hu, Anren., Wu, Hui-Chung., Ye, Shu-Ping., Ho, Kuo-Chieh., Chen, Liang-Yu. Toxicity attenuation of atractyloside in traditional chinese medicinal herbs after hydrothermal processing . Botanical studies, 2012, vol. 53, no. 4, p. 459-465.
  11. McMillan, C., Chavez, P.I., Mabry, T.J. Sesquiterpene lactones of Xanthium strumarium in a texas population and in experimental hybrids. Biochemical systematics and ecology, 1975, vol. 3, no. 3, p. 137-141. DOI
  12. Kim, YS., Kim, JS., Park, SH., Choi, SU., Lee, CO., Kim, SK., Kim, YK., Kim, SH., Ryu, SY. Two cytotoxic sesquiterpene lactones from the leaves of Xanthium strumarium and their in vitro inhibitory activity on farnesyltransferase . Planta medica, 2003, vol. 69, no. 4, p. 375-377. DOI

Boundary

A constituent measurement is a fact about material at a stated preparation, not a statement about what that material does in a person. An adverse-effect or genotoxicity record is an observation reported in a source, most often in an animal or laboratory model. Neither is a Metatron Health conclusion about causality, human risk or benefit, and the absence of a record is not proof that a preparation is safe. Nothing here is diagnosis, prescribing or individual medical care.

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