Botanical species · safety record

Mitragyna speciosa

The EFSA Compendium of Botanicals holds 39 constituent measurements, 19 adverse-effect records and 1 genotoxicity assay for Mitragyna speciosa. 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: Mitragyna speciosa (Korth. ) Havil.

39Constituent measurements
20Safety records
11Cited sources
2Licensed products (Canada)

Regulatory presence

Health Canada's Licensed Natural Health Products Database holds 2 licensed products naming Mitragyna speciosa as a medicinal ingredient, matched on the exact Latin binomial. A licence records that a product met the regulator's requirements for sale in Canada. It is not evidence that the product works.

Source material stated

  • Leaf

What the records describe

Constituents measured

  • Alkaloids14
  • Mitragynine12
  • 7-hydroxymitragynine5
  • Acetaldehyde3
  • Ajmalicine1
  • Epigallocatechin1
  • Gallic acid1
  • Methanoic acid1
  • Triterpene saponins1

Plant parts

  • Leaves50
  • Unspecified4
  • Stem3
  • stalk3
  • Roots and other underground parts1

Preparations

  • Solvent extraction39

Effect types

  • Pulmonary and cardiac5
  • Systemic3
  • Hepatotoxicity2
  • Neurotoxicity2
  • Developmental1
  • Digestive1
  • Hemopoietic1
  • Musclo-skeletal1
  • Nephrotoxicity1
  • Other toxicities1

Target tissues

  • Lung4
  • Liver3
  • Digestive2
  • Skin2
  • subcutis2
  • Brain1
  • Muscle, skeletal1
  • Neurologic1
  • Neurologic: central nervous system1
  • Urogenital: kidneys1

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
7-hydroxymitragynineLeavesSolvent extraction≤ 0.361 Milligram/gramChromatographic testsResolve DOI
7-hydroxymitragynineLeavesSolvent extraction≥ 0.114 Milligram/gramChromatographic testsResolve DOI
7-hydroxymitragynineLeavesSolvent extractionGC-MSResolve DOI
7-hydroxymitragynineLeaves2 PercentUnspecifiedResolve DOI
AlkaloidsLeavesSolvent extractionGC-MSResolve DOI
AlkaloidsLeaves≤ 9 PercentUnspecifiedResolve DOI
AlkaloidsLeaves< 1 PercentUnspecifiedResolve DOI
AlkaloidsLeavesSolvent extractionGC-MSResolve DOI
AlkaloidsLeaves< 1 PercentUnspecifiedResolve DOI
AlkaloidsLeaves< 1 PercentUnspecifiedResolve DOI
AlkaloidsLeaves< 1 PercentUnspecifiedResolve DOI
AlkaloidsLeavesSolvent extractionGC-MSResolve DOI
AlkaloidsLeaves10 PercentUnspecifiedResolve DOI
AlkaloidsLeaves< 1 PercentUnspecifiedResolve DOI
AlkaloidsLeavesSolvent extractionGC-MSResolve DOI
AlkaloidsLeaves≥ 7 PercentUnspecifiedResolve DOI
MitragynineLeaves60 PercentUnspecifiedResolve DOI
MitragynineLeavesSolvent extraction1.6 PercentGC-MSResolve DOI
MitragynineLeavesSolvent extraction≤ 21.2 Milligram/gramChromatographic testsResolve DOI
MitragynineLeavesSolvent extraction≥ 0.8 Milligram/gramChromatographic testsResolve DOI
MitragynineLeavesSolvent extraction≤ 3.04 Milligram/gramGC-MSResolve DOI
MitragynineLeavesSolvent extraction≥ 0.64 Milligram/gramGC-MSResolve DOI
7-hydroxymitragynineLeavesSolvent extractionChromatographic testsNo resolvable identifier
AcetaldehydeLeavesSolvent extraction9.36 Milligram/gramHigh Performance Liquid Chromatography (HPLC)/Liquid Chromatography (LC)No resolvable identifier
AcetaldehydeRoots and other underground partsSolvent extraction4.11 Milligram/gramHigh Performance Liquid Chromatography (HPLC)/Liquid Chromatography (LC)No resolvable identifier
AcetaldehydeStem / stalkSolvent extraction4.11 Milligram/gramHigh Performance Liquid Chromatography (HPLC)/Liquid Chromatography (LC)No resolvable identifier
AjmalicineLeavesSolvent extractionChromatographic testsNo resolvable identifier
AlkaloidsLeavesSolvent extractionHigh Performance Liquid Chromatography (HPLC)/Liquid Chromatography (LC)No resolvable identifier
AlkaloidsLeavesSolvent extractionChromatographic testsNo resolvable identifier
EpigallocatechinLeavesSolvent extractionNuclear Magnetic Resonance (NMR) and Electron Spin Resonance (ESR) spectroscopyNo resolvable identifier
Gallic acidLeavesSolvent extractionNuclear Magnetic Resonance (NMR) and Electron Spin Resonance (ESR) spectroscopyNo resolvable identifier
Methanoic acidLeavesSolvent extractionNuclear Magnetic Resonance (NMR) and Electron Spin Resonance (ESR) spectroscopyNo resolvable identifier
MitragynineLeavesSolvent extraction0.4 Microgram/millilitreHigh Performance Liquid Chromatography (HPLC)/Liquid Chromatography (LC)No resolvable identifier
MitragynineLeavesSolvent extraction≤ 4.01 Milligram/gramHigh Performance Liquid Chromatography (HPLC)/Liquid Chromatography (LC)No resolvable identifier
MitragynineLeavesSolvent extraction≥ 3.96 Milligram/gramHigh Performance Liquid Chromatography (HPLC)/Liquid Chromatography (LC)No resolvable identifier
MitragynineStem / stalkSolvent extraction≤ 1.22 Milligram/gramHigh Performance Liquid Chromatography (HPLC)/Liquid Chromatography (LC)No resolvable identifier
MitragynineStem / stalkSolvent extraction≥ 0.78 Milligram/gramHigh Performance Liquid Chromatography (HPLC)/Liquid Chromatography (LC)No resolvable identifier
MitragynineLeavesSolvent extractionChromatographic testsNo resolvable identifier
Triterpene saponinsLeavesSolvent extractionChromatographic testsNo 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
DevelopmentalDigestiveLeavesSolvent extractionRat (as animal)Short-term toxicityResolve DOI
DigestiveDigestiveLeavesHuman (as organism)Acute toxicityResolve DOI
HemopoieticLeavesSolvent extractionRat (as animal)Acute toxicityResolve DOI
HepatotoxicityLiverLeavesSolvent extractionRat (as animal)Short-term toxicityResolve DOI
HepatotoxicityLiverLeavesSolvent extractionRat (as animal)Short-term toxicityResolve DOI
Musclo-skeletalMuscle, skeletalLeavesHuman (as organism)Acute toxicityResolve DOI
NephrotoxicityUrogenital: kidneysLeavesSolvent extractionRat (as animal)Short-term toxicityResolve DOI
NeurotoxicityBrainLeavesSolvent extractionRat (as animal)Short-term toxicityResolve DOI
NeurotoxicityNeurologicLeavesHuman (as organism)Acute toxicityResolve DOI
Other toxicitiesLeavesHuman (as organism)Acute toxicityResolve DOI
Pulmonary and cardiacLeavesHuman (as organism)Acute toxicityResolve DOI
Pulmonary and cardiacLungUnspecifiedHuman (as organism)Case reportResolve DOI
Pulmonary and cardiacLungUnspecifiedHuman (as organism)Case reportResolve DOI
Pulmonary and cardiacLungUnspecifiedHuman (as organism)Case reportResolve DOI
Pulmonary and cardiacLungUnspecifiedHuman (as organism)Case reportResolve DOI
SystemicSkin/subcutisLeavesSolvent extractionRat (as animal)Short-term toxicityResolve DOI
SystemicNeurologic: central nervous systemLeavesSolvent extractionRat (as animal)Short-term toxicityResolve DOI
SystemicSkin/subcutisLeavesSolvent extractionRat (as animal)Short-term toxicityResolve DOI
Not statedLiverLeavesSolvent extractionRat (as animal)Acute toxicityResolve DOI

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 repairDNA damage and repair assay, unscheduled DNA synthesis in mammalian cells in vitroOtherResolve 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. Trakulsrichai, Satariya., Tongpo, Achara., Sriapha, Charuwan., Wongvisawakorn, Sunun., Rittilert, Panee., Kaojarern, Sming., Wananukul, Winai. Kratom Abuse in Ramathibodi Poison Center, Thailand: A Five-Year Experience . Journal of psychoactive drugs, 2013, vol. 45, no. 5, p. 404-408. DOI
  2. Karinen, Ritva., Fosen, Jan Toralf., Rogde, Sidsel., Vindenes, Vigdis. An accidental poisoning with mitragynine. Forensic science international, 2014, vol. 245, p. E29-E32. DOI
  3. Harizal, S. N., Mansor, S. M., Hasnan, J., Tharakan, J. K. J., Abdullah, J. Acute toxicity study of the standardized methanolic extract of Mitragyna speciosa Korth in Rodent . Journal of ethnopharmacology, 2010, vol. 131, no. 2, p. 404-409. DOI
  4. Charoonratana, Tossaton., Wungsintaweekul, Juraithip., Pathompak, Pathamaporn., Georgiev, Milen I., Choi, Young Hae., Verpoorte, Robert. Limitation of Mitragynine Biosynthesis in Mitragyna speciosa (Roxb.) Korth. through Tryptamine Availability . Zeitschrift fur naturforschung section c-a journal of biosciences, 2013, vol. 68, no. 9-10, p. 394-405.
  5. Kapp, Friedrich G., Maurer, Hans H., Auwarter, Volker., Winkelmann, Martin., Hermanns-Clausen, Maren. Intrahepatic cholestasis following abuse of powdered kratom (Mitragyna speciosa). . Journal of medical toxicology : official journal of the american college of medical toxicology, 2011, vol. 7, no. 3, p. 227-31. DOI
  6. Kikura-Hanajiri, Ruri., Kawamura, Maiko., Maruyama, Takuro., Kitajima, Mariko., Takayama, Hiromitsu., Goda, Yukihiro. Simultaneous analysis of mitragynine, 7-hydroxymitragynine, and other alkaloids in the psychotropic plant kratom (Mitragyna speciosa) by LC-ESI-MS . Forensic toxicology, 2009, vol. 27, no. 2, p. 67-74. DOI
  7. Oliveira, Ana Sofia., Fraga, Sonia., Carvalho, Felix., Araujo, Ana Margarida., Pereira, Cristiana Costa., Teixeira, Joao Paulo., Bastos, Maria de Lourdes., de Pinho, Paula Guedes. Chemical characterization and in vitro cyto- and genotoxicity of 'legal high' products containing Kratom (Mitragyna speciosa) . Forensic toxicology, 2016, vol. 34, no. 2, p. 213-226. DOI
  8. Warner, Marcus L., Kaufman, Nellie C., Grundmann, Oliver. The pharmacology and toxicology of kratom: from traditional herb to drug of abuse . International journal of legal medicine, 2016, vol. 130, no. 1, p. 127-138. DOI
  9. Kong Wai Mun., Chik Zamri., Mohamed Zahurin., Alshawsh Mohammed A. Physicochemical Characterization of Mitragyna speciosa Alkaloid Extract and Mitragynine Using In Vitro High Throughput Assays. Combinatorial chemistry & high throughput screening, 2017, p. Combinatorial chemistry & high throughput screening (2017).
  10. Sabetghadam, Azadeh., Ramanathan, Surash., Sasidharan, Sreenivasan., Mansor, Sharif Mahsufi. Subchronic exposure to mitragynine, the principal alkaloid of Mitragyna speciosa, in rats . Journal of ethnopharmacology, 2013, vol. 146, no. 3, p. 815-823. DOI
  11. Leon, Francisco., Habib, Eman., Adkins, Jessica E., Furr, Edward B., McCurdy, Christopher R., Cutler, Stephen J. Phytochemical Characterization of the Leaves of Mitragyna speciosa Grown in USA . Natural product communications, 2009, vol. 4, no. 7, p. 907-910.

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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