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.
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
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.
| Substance | Plant part | Preparation | Concentration | Analytical method | Source |
|---|---|---|---|---|---|
| 7-hydroxymitragynine | Leaves | Solvent extraction | ≤ 0.361 Milligram/gram | Chromatographic tests | Resolve DOI |
| 7-hydroxymitragynine | Leaves | Solvent extraction | ≥ 0.114 Milligram/gram | Chromatographic tests | Resolve DOI |
| 7-hydroxymitragynine | Leaves | Solvent extraction | — | GC-MS | Resolve DOI |
| 7-hydroxymitragynine | Leaves | — | 2 Percent | Unspecified | Resolve DOI |
| Alkaloids | Leaves | Solvent extraction | — | GC-MS | Resolve DOI |
| Alkaloids | Leaves | — | ≤ 9 Percent | Unspecified | Resolve DOI |
| Alkaloids | Leaves | — | < 1 Percent | Unspecified | Resolve DOI |
| Alkaloids | Leaves | Solvent extraction | — | GC-MS | Resolve DOI |
| Alkaloids | Leaves | — | < 1 Percent | Unspecified | Resolve DOI |
| Alkaloids | Leaves | — | < 1 Percent | Unspecified | Resolve DOI |
| Alkaloids | Leaves | — | < 1 Percent | Unspecified | Resolve DOI |
| Alkaloids | Leaves | Solvent extraction | — | GC-MS | Resolve DOI |
| Alkaloids | Leaves | — | 10 Percent | Unspecified | Resolve DOI |
| Alkaloids | Leaves | — | < 1 Percent | Unspecified | Resolve DOI |
| Alkaloids | Leaves | Solvent extraction | — | GC-MS | Resolve DOI |
| Alkaloids | Leaves | — | ≥ 7 Percent | Unspecified | Resolve DOI |
| Mitragynine | Leaves | — | 60 Percent | Unspecified | Resolve DOI |
| Mitragynine | Leaves | Solvent extraction | 1.6 Percent | GC-MS | Resolve DOI |
| Mitragynine | Leaves | Solvent extraction | ≤ 21.2 Milligram/gram | Chromatographic tests | Resolve DOI |
| Mitragynine | Leaves | Solvent extraction | ≥ 0.8 Milligram/gram | Chromatographic tests | Resolve DOI |
| Mitragynine | Leaves | Solvent extraction | ≤ 3.04 Milligram/gram | GC-MS | Resolve DOI |
| Mitragynine | Leaves | Solvent extraction | ≥ 0.64 Milligram/gram | GC-MS | Resolve DOI |
| 7-hydroxymitragynine | Leaves | Solvent extraction | — | Chromatographic tests | No resolvable identifier |
| Acetaldehyde | Leaves | Solvent extraction | 9.36 Milligram/gram | High Performance Liquid Chromatography (HPLC)/Liquid Chromatography (LC) | No resolvable identifier |
| Acetaldehyde | Roots and other underground parts | Solvent extraction | 4.11 Milligram/gram | High Performance Liquid Chromatography (HPLC)/Liquid Chromatography (LC) | No resolvable identifier |
| Acetaldehyde | Stem / stalk | Solvent extraction | 4.11 Milligram/gram | High Performance Liquid Chromatography (HPLC)/Liquid Chromatography (LC) | No resolvable identifier |
| Ajmalicine | Leaves | Solvent extraction | — | Chromatographic tests | No resolvable identifier |
| Alkaloids | Leaves | Solvent extraction | — | High Performance Liquid Chromatography (HPLC)/Liquid Chromatography (LC) | No resolvable identifier |
| Alkaloids | Leaves | Solvent extraction | — | Chromatographic tests | No resolvable identifier |
| Epigallocatechin | Leaves | Solvent extraction | — | Nuclear Magnetic Resonance (NMR) and Electron Spin Resonance (ESR) spectroscopy | No resolvable identifier |
| Gallic acid | Leaves | Solvent extraction | — | Nuclear Magnetic Resonance (NMR) and Electron Spin Resonance (ESR) spectroscopy | No resolvable identifier |
| Methanoic acid | Leaves | Solvent extraction | — | Nuclear Magnetic Resonance (NMR) and Electron Spin Resonance (ESR) spectroscopy | No resolvable identifier |
| Mitragynine | Leaves | Solvent extraction | 0.4 Microgram/millilitre | High Performance Liquid Chromatography (HPLC)/Liquid Chromatography (LC) | No resolvable identifier |
| Mitragynine | Leaves | Solvent extraction | ≤ 4.01 Milligram/gram | High Performance Liquid Chromatography (HPLC)/Liquid Chromatography (LC) | No resolvable identifier |
| Mitragynine | Leaves | Solvent extraction | ≥ 3.96 Milligram/gram | High Performance Liquid Chromatography (HPLC)/Liquid Chromatography (LC) | No resolvable identifier |
| Mitragynine | Stem / stalk | Solvent extraction | ≤ 1.22 Milligram/gram | High Performance Liquid Chromatography (HPLC)/Liquid Chromatography (LC) | No resolvable identifier |
| Mitragynine | Stem / stalk | Solvent extraction | ≥ 0.78 Milligram/gram | High Performance Liquid Chromatography (HPLC)/Liquid Chromatography (LC) | No resolvable identifier |
| Mitragynine | Leaves | Solvent extraction | — | Chromatographic tests | No resolvable identifier |
| Triterpene saponins | Leaves | Solvent extraction | — | Chromatographic tests | 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.
| Effect | Target tissue | Plant part | Preparation | Test organism | Test type | Source |
|---|---|---|---|---|---|---|
| Developmental | Digestive | Leaves | Solvent extraction | Rat (as animal) | Short-term toxicity | Resolve DOI |
| Digestive | Digestive | Leaves | — | Human (as organism) | Acute toxicity | Resolve DOI |
| Hemopoietic | — | Leaves | Solvent extraction | Rat (as animal) | Acute toxicity | Resolve DOI |
| Hepatotoxicity | Liver | Leaves | Solvent extraction | Rat (as animal) | Short-term toxicity | Resolve DOI |
| Hepatotoxicity | Liver | Leaves | Solvent extraction | Rat (as animal) | Short-term toxicity | Resolve DOI |
| Musclo-skeletal | Muscle, skeletal | Leaves | — | Human (as organism) | Acute toxicity | Resolve DOI |
| Nephrotoxicity | Urogenital: kidneys | Leaves | Solvent extraction | Rat (as animal) | Short-term toxicity | Resolve DOI |
| Neurotoxicity | Brain | Leaves | Solvent extraction | Rat (as animal) | Short-term toxicity | Resolve DOI |
| Neurotoxicity | Neurologic | Leaves | — | Human (as organism) | Acute toxicity | Resolve DOI |
| Other toxicities | — | Leaves | — | Human (as organism) | Acute toxicity | Resolve DOI |
| Pulmonary and cardiac | — | Leaves | — | Human (as organism) | Acute toxicity | Resolve DOI |
| Pulmonary and cardiac | Lung | Unspecified | — | Human (as organism) | Case report | Resolve DOI |
| Pulmonary and cardiac | Lung | Unspecified | — | Human (as organism) | Case report | Resolve DOI |
| Pulmonary and cardiac | Lung | Unspecified | — | Human (as organism) | Case report | Resolve DOI |
| Pulmonary and cardiac | Lung | Unspecified | — | Human (as organism) | Case report | Resolve DOI |
| Systemic | Skin/subcutis | Leaves | Solvent extraction | Rat (as animal) | Short-term toxicity | Resolve DOI |
| Systemic | Neurologic: central nervous system | Leaves | Solvent extraction | Rat (as animal) | Short-term toxicity | Resolve DOI |
| Systemic | Skin/subcutis | Leaves | Solvent extraction | Rat (as animal) | Short-term toxicity | Resolve DOI |
| Not stated | Liver | Leaves | Solvent extraction | Rat (as animal) | Acute toxicity | Resolve 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.
| Outcome | Endpoint | Test | Tested organism | Metabolic activation | Source |
|---|---|---|---|---|---|
| Positive | DNA damage and/or repair | DNA damage and repair assay, unscheduled DNA synthesis in mammalian cells in vitro | Other | — | Resolve 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.
- 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
- Karinen, Ritva., Fosen, Jan Toralf., Rogde, Sidsel., Vindenes, Vigdis. An accidental poisoning with mitragynine. Forensic science international, 2014, vol. 245, p. E29-E32. DOI
- 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
- 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.
- 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
- 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
- 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
- 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
- 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).
- 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
- 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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