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Revision as of 19:07, 26 June 2013 editZad68 (talk | contribs)Extended confirmed users20,355 edits antioxidant effects/catechin - insufficient fidelity to source, which states only that epicatechin is present but not an "active" component, no health effects described in source given← Previous edit Revision as of 19:14, 26 June 2013 edit undoZad68 (talk | contribs)Extended confirmed users20,355 edits Anti-depressant effects - rm speculative effects based on primary mouse studyNext edit →
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==Medicinal uses== ==Medicinal uses==
Kratom has seen therapeutic use in Thai ] as an ], as a treatment for ], and rarely to increase the duration of ].<ref name="Suwanlert 1975">{{cite journal | title = A Study of Kratom Eaters in Thailand | journal = Bulletin on Narcotics | year = 1975 | first = Sangun | last = Suwanlert | volume = 27 | issue = 3 | pages = 21–27 | accessdate = 2012-10-26}}</ref><ref name="Jansen 1988-01-04">{{cite journal | title = Ethnopharmacology of Kratom and the Mitragyna Alkaloids | journal = Journal of Ethnophamacology | date = 1988-01-04 | first = Karl L.R. | last = Jansen | coauthors = Colin J. Prast | volume = 23 | issue = 1 | pages = 115–119 | pmid = 3419199 | issn = 0378-8741| accessdate = 2012-10-26}}</ref><ref name="Reanmongkol 2007">{{cite journal | title = Effects of the extracts from Mitragyna speciosa Korth. leaves on analgesic and behavioral activities in experimental animals | journal = Songklanakarin Journal of Science and Technology | date = March 2007 | first = Wantana | last = Reanmongkol | coauthors = Niwat Keawpradub, Kitja Sawangjaroen | volume = 29 | issue = 1 | pages = 39–48 | url = http://www.thaiscience.info/journals/Article/Effects%20of%20the%20extracts%20from%20mitragyna%20speciosa%20korth%2E%20leaves%20on%20analgesic%20and%20behavioral%20activities%20in%20experimental%20animals.pdf | format = PDF | accessdate = 2012-10-26}}</ref> A general consensus exists in Thailand among leaders, public health officials, academics and policymakers that kratom use and dependence causes little, if any, health risks.<ref name="Decriminalization and Community Control?"/> Kratom has seen therapeutic use in Thai ] as an ], as a treatment for ], and rarely to increase the duration of ].<ref name="Suwanlert 1975">{{cite journal | title = A Study of Kratom Eaters in Thailand | journal = Bulletin on Narcotics | year = 1975 | first = Sangun | last = Suwanlert | volume = 27 | issue = 3 | pages = 21–27 | accessdate = 2012-10-26}}</ref><ref name="Jansen 1988-01-04">{{cite journal | title = Ethnopharmacology of Kratom and the Mitragyna Alkaloids | journal = Journal of Ethnophamacology | date = 1988-01-04 | first = Karl L.R. | last = Jansen | coauthors = Colin J. Prast | volume = 23 | issue = 1 | pages = 115–119 | pmid = 3419199 | issn = 0378-8741| accessdate = 2012-10-26}}</ref><ref name="Reanmongkol 2007">{{cite journal | title = Effects of the extracts from Mitragyna speciosa Korth. leaves on analgesic and behavioral activities in experimental animals | journal = Songklanakarin Journal of Science and Technology | date = March 2007 | first = Wantana | last = Reanmongkol | coauthors = Niwat Keawpradub, Kitja Sawangjaroen | volume = 29 | issue = 1 | pages = 39–48 | url = http://www.thaiscience.info/journals/Article/Effects%20of%20the%20extracts%20from%20mitragyna%20speciosa%20korth%2E%20leaves%20on%20analgesic%20and%20behavioral%20activities%20in%20experimental%20animals.pdf | format = PDF | accessdate = 2012-10-26}}</ref> A general consensus exists in Thailand among leaders, public health officials, academics and policymakers that kratom use and dependence causes little, if any, health risks.<ref name="Decriminalization and Community Control?"/>

===Anti-depressant effects===
Kratom is traditionally used to treat symptoms of depression. A study of mitragynine, isolated from ''Mitragyna speciosa'', concluded that the substance showed significant anti-depressant effects in mice, improving their performance in the Forced Swim Test and Tail Suspension Test.<ref>{{Cite pmid|20869223}}</ref>


===Improving high blood-pressure=== ===Improving high blood-pressure===

Revision as of 19:14, 26 June 2013

Mitragyna speciosa
Scientific classification
Kingdom: Plantae
Division: Magnoliophyta
Class: Magnoliopsida
Order: Gentianales
Family: Rubiaceae
Genus: Mitragyna
Species: M. speciosa
Binomial name
Mitragyna speciosa
(Korth.) Havil.
Synonyms
  • Nauclea korthalsii Steud. nom. inval.
  • Nauclea luzoniensis Blanco
  • Nauclea speciosa (Korth.) Miq.
  • Stephegyne speciosa Korth.

Mitragyna speciosa (kratom, kratum, krathom, Thai: กระท่อม) is a tropical deciduous and evergreen tree in the coffee family (Rubiaceae) native to Southeast Asia in the Indochina and Malesia floristic regions. Its leaves are used for medicinal properties. It is psychoactive, and leaves are chewed to uplift mood and to treat health problems. M. speciosa is indigenous to Thailand and, despite growing naturally in the country, has been outlawed for 70 years and was originally banned because it was reducing the Thai government's tax revenue from opium distribution.

Most side effects of Mitragyna speciosa are thought to be mild, although serious adverse effects such as psychosis, convulsions, hallucinations, and confusion have been reported. Chronic use of M. speciosa has been associated with bowel obstruction, and the plant carries the potential for addiction and can lead to withdrawal symptoms. M. speciosa may be mixed or co-ingested with dextromethorphan-containing cough syrup, amphetamines, or benzodiazepines with harmful results.

Taxonomy and description

It was first formally described by the Dutch colonial botanist Pieter Korthals. The genus was named Mitragyna by Korthals because the stigmas in the first species he examined resembled the shape of a bishop's mitre. It is botanically related to the genera Corynanthe and Uncaria and shares some similar biochemistry.

Close up of Healthy dark green Kratom leaf

Mitragyna speciosa trees usually grow to a height of 12–30 ft (3.7–9.1 m) tall and 15 ft (4.6 m) wide, although some species can reach 40–100 ft (12–30 m) in height. Mitragyna speciosa can be either evergreen or deciduous depending on the climate and environment in which it is grown. The stem is erect and branching. The leaves of the kratom tree are a dark green colour and can grow to over 7 inches (180 mm) long and 4 inches (100 mm) wide, are ovate-acuminate in shape, and opposite in growth pattern. The flowers are yellow and round and tend to grow in clusters at the end of the branches. The leaves of M. Speciosa are elliptic and are smaller at the end of the branchlets and are pointed at the tip. The leaves have a round and heart-shape at the base with the petioles between 2 to 4 centimeters long. The flowers are crowded in a round terminal inflorescences which are three to five centimeters long. The calyx-tube is short and cup-shaped, with round lobes. The corolla-tube is five millimeters long with three millimiter long lobes and smooth and revolute in between.

Chemistry

Kratom leaves
Young M. Speciosa tree

There are 40 compounds in M. Speciosa leaves, including many alkaloids including mitragynine (once thought to be the primary active constituent), mitraphylline, and 7-hydroxymitragynine (which is currently the most likely candidate for the primary active chemical in the plant). Other active chemicals in M. Speciosa include raubasine (best known from Rauwolfia serpentina) and some yohimbe alkaloids such as corynantheidine.

Mitragyna Speciosa also contains at least one alkaloid (rhynchophylline) that is a calcium channel blocker, and reduces NMDA-induced current. There is considerable research as to the role of NMDA receptor activity in the formation of dependence, and the symptoms of withdrawal. In 2005, Inturrisi demonstrated that co-administration of d-methadone (the isomer that lacks opioid activity, but is an NMDA antagonist) in small doses with morphine prevented the development of morphine tolerance in rats. The presence of mitragynine can be detected in urine by non-conventional immunological screenings.

The amount of mitragynine within the leaves depends highly on many factors, one major factor is the location of the tree. When trees are grown in Southeast Asia, the levels tend to be higher but when grown elsewhere (even in greenhouses) the levels tend to be low or non-existent. One analysis of products marketed as kratom leaf found, using liquid chromatography-electrospray ionization mass spectrometry (LC-ESI-MS), mitragynine at levels of 1-6% and 7-hydroxymirtrogynine at levels of 0.01-0.04%. The chemical structure of mitragynines incorporate the nucleus of the tryptamine, and these may be responsible for the molecules which are observed in the serotonin and adrnergic systems. In mitragynine, the phenolic methyl ether is considered to be stronger in analgesic paradigms according to some studies. Moreover, studies concerning the pharmacokinetics of M. Speciosa in humans has not been well studied and various aspects such as the half-life, protein binding properties and other properties such as the elimination or metabolism is not known.

Traditional use

Kratom has been traditionally chewed, in raw leaf form, by people in Thailand and especially in the southern peninsula. Kratom is also used in neighboring countries in Southeast Asia where it grows naturally. As traditionally used, kratom is not seen as a drug and there is no stigma associated with kratom use or discrimination against kratom eaters. In southern Thailand, kratom has been a part of traditional culture for thousands of years and is common in traditional cultural performances and in agriculture. In southern Thailand, kratom chewers generally start at around the age of 25 and many continue to chew the leaves for the rest of their lives. The average number of leaves consumed is between 10 and 60 leaves consumed daily, but even more than this is common. In southern Thailand, upwards of 70% of the male population uses kratom on a daily basis in some areas. Traditional use of kratom is considered equivalent to drinking coffee.

M. Speciosa tree branch

As with any substance that is ingested, adulteration or contamination is also a risk. One product, Krypton that contained a mix of several different substances rather than natural kratom was linked to the deaths of nine people in Sweden during 2010-2011. Krypton contained O-desmethyltramadol which is the active metabolite in tramadol. O-desmethyltramadol is a considerably more potent μ-opioid agonist than Tramadol, its parent compound. Since it is possible to overdose on Tramadol alone, it can be assumed its more potent active metabolite, O-desmethyltramadol, causes fatalities as well.

However, there has never been a single documented lethal case of kratom overdose.

Medicinal uses

Kratom has seen therapeutic use in Thai ethnomedicine as an antidiarrhoeal, as a treatment for opioid dependence, and rarely to increase the duration of coitus. A general consensus exists in Thailand among leaders, public health officials, academics and policymakers that kratom use and dependence causes little, if any, health risks.

Improving high blood-pressure

One active alkaloid in M. speciosa is Ajmalicine, which is also known as "raubasine" or "δ-yohimbine" and is used as an antihypertensive drug used in the treatment of high blood pressure.

Media attention

Kratom, like other herbs with drug-like properties, is frequently a concern of politicians, journalists and regulatory officials. No scientific reports exist proving kratom alone results in lethal overdose. A recent incident involving a 27 year old woman from Kelso, Washington was blamed on kratom consumption. The woman was arrested after being caught naked running in the street with a hammer. According to reports she had smoked marijuana laced with chemicals prior to this incident in addition to consuming kratom.

Regulation

Kratom leaf

Kratom alone, when chewed or boiled into a tea, is indeed quite harmless according to the available literature. While additional research is needed, it has been said that the criminalization of kratom is unfounded and is based on economic control and disinformation. There are very few records available showing negative health or social consequences from kratom consumption, but despite this fact kratom is becoming increasingly subject to actions of law enforcement in numerous countries. The criminalization of kratom has created numerous barriers for research. In Thailand, the eradication campaigns have made it especially difficult for academics and researchers to adequately research the medicinal benefits of kratom. It has been recommended by the transnational institute that kratom be decriminalized and has concluded that the criminalization of kratom to be unnecessary, problematic and counter-productive. It also concluded that the evidence showing the health benefits of kratom, especially in treating drug and alcohol dependence, should serve as an important point to consider.

Thailand

Prohibition

Possession of kratom leaves is illegal in Thailand, despite the tree being native to the country. The Thai government passed the Kratom Act 2486 which went into effect on August 3, 1943. This law makes planting the tree illegal and requires existing trees to be cut down. This law was not found effective, since the tree is indigenous to the country. Today, kratom is scheduled in category 5 of the Narcotics Acts (1979), in the same category as cannabis and magic mushrooms (the least punitive category). A large aspect of Thai culture supports kratom, however despite this fact the Thai government has initiated a program of destroying kratom trees by burning forests or chopping large sections of kratom forests down. Eradication campaigns often destroy not only the trees but also other trees and wildlife in these areas, which are often untouched rainforests with sensitive ecosystems.

Proposed decriminalization

In 2010, the Thai Office of the Narcotics Control Board proposed decriminalizing kratom and affirmed its use as an integral part of Thai culture. The ONCB concluded that decades of unproblematic use, and an absence of health and social harm, make prohibiting the leaf unnecessary and counterproductive. According to the ONCB's report, kratom was in fact banned for economic reasons, not for health or social concerns. In a snippet from a book written by Cassandra Hoffman:

"In Thailand, kratom was first scheduled for control in 1943 under the Kratom Act. At the time, the government was levying taxes from users and shops involved in the opium trade. Because of the increasing opium costs, many users were switching to kratom to manage their withdrawal symptoms. However, the launch of the Greater East Asia War in 1942 and declining revenues from the opium trade pushed the Thai government into action to curb and suppress competition in the opium market by making kratom illegal."

While additional research is needed kratom proponents argue that the criminalization of kratom is unfounded and is based on economic control and misinformation. The criminalization of kratom has made research more difficult, especially in Thailand. It has been recommended by the Transnational Institute that kratom be decriminalized and that the criminalization of kratom to be unnecessary, problematic and counter-productive. The Institute also argues that the evidence showing the health benefits of kratom, particularly in treating drug and alcohol dependence, are worth exploring further.

United States

Kratom itself is not regulated by the United States federal government, though the Drug Enforcement Administration includes the tree in its "Drug and Chemical of Concern" list.

Indiana House of Representatives HB1196, sponsored by Edward DeLaney, Steve Davisson, Terri Austin, Vernon G. Smith, and David Yarde during the 2012 regular session as a response to increasing synthetic drug use, made Indiana the first and only state to ban kratom, although indirectly. The text of the bill added kratom's two active alkaloids—mitragynine and 7-hydroxymitragynine—to the state's list of controlled substances, though kratom itself is not synthetic and was not specifically addressed by the authors of the bill. Petitioners on Change.org subsequently sought delisting of kratom's alkaloids by raising the issue with Indiana Governor Mitch Daniels.

Iowa legislators grouped Mitragyna speciosa as a synthetic cannabinoid when a bill was proposed that would reclassify nearly all controlled substances in their state. The Louisiana legislature proposed an age limit of 18 to be able to legally purchase, possess and consume kratom. Violators would have been assessed a penalty of no more than $500, or sentenced to six months in jail, or both. Massachusetts Representative Daniel K. Webster sponsored legislation in 2011 that would have included compounds of Mitragyna speciosa in the state's controlled substance classification list.

See also

References

  1. "The Plant List: A Working List of All Plant Species".
  2. "USDA GRIN Taxonomy".
  3. ^ Kratom in Thailand: Decriminalization and Community Control? Proposal by the Thai Office of the Narcotics Control Board (PDF) Cite error: The named reference "Decriminalization and Community Control?" was defined multiple times with different content (see the help page).
  4. Philippine Department of Agriculture - Bureau of Plant Industry: Eintrag Mambog)
  5. Adkins, Jessica E. (2011-05-01). "Mitragyna speciosa, a psychoactive tree from Southeast Asia with opioid activity". Current Topics in Medicinal Chemistry. 11 (9): 1165–1175. doi:10.2174/156802611795371305. PMID 21050173. {{cite journal}}: |access-date= requires |url= (help); Unknown parameter |coauthors= ignored (|author= suggested) (help)
  6. Chittrakarn, S; Keawpradub, N; Sawangjaroen, K; Kansenalak, S; Janchawee, B (2010). "The neuromuscular blockade produced by pure alkaloid, mitragynine and methanol extract of kratom leaves (Mitragyna speciosa Korth.)". Journal of Ethnopharmacology. 129 (3): 344–349. doi:10.1016/j.jep.2010.03.035. PMID 20371282.
  7. ^ Prozialeck, WC; Jivan, JK; Andurkar, SV (2012). "Pharmacology of kratom: an emerging botanical agent with stimulant, analgesic, and opioid-like effects". The Journal of the American Osteopathic Association. 112 (12): 792–799. PMID 23212430.
  8. Takayama H, Ishikawa H, Kurihara M, Kitajima M, Aimi N, Ponglux D; et al. (2002). "Studies on the synthesis and opioid agonistic activities of mitragynine-related indole alkaloids: discovery of opioid agonists structurally different from other opioid ligands". J Med Chem. 45 (9): 1949–1956. doi:10.1021/jm010576e. PMID 11960505. {{cite journal}}: Explicit use of et al. in: |author= (help)CS1 maint: multiple names: authors list (link)
  9. Microgram Bulletin - Department of Justice
  10. Hendrickson, JB, Sims JJ. Mitragyna alkaloids - The structure of stipulatine. Tetrahedron Letters 1963;14:959-963.
  11. Inturrisi, CE. Minerva Anestesiology 71, 435-437. 2005.
  12. Kratom alkaloids and O-desmethyltramadol in urine of a "Krypton" herbal mixture consumer, doi:10.1016/j.forsciint.2010.10.025, PMID 21112167
  13. Leon, F; Habib, E; Adkins, Je (2009). "Phytochemical characterization of the leaves of Mitragyna speciosa grown in U.S.A." Nat Prod Commun. 112 (7): 907–910. PMID 19731590.
  14. Kikura-Hanajiri, Ruri (1). "Simultaneous analysis of mitragynine, 7-hydroxymitragynine, and other alkaloids in the psychotropic plant "kratom" (Mitragyna speciosa) by LC-ESI-MS". Forensic Toxicology. 27 (2): 67–74. doi:10.1007/s11419-009-0070-5. Retrieved 23 June 2013. {{cite journal}}: Check date values in: |date= and |year= / |date= mismatch (help); Unknown parameter |coauthors= ignored (|author= suggested) (help); Unknown parameter |month= ignored (help)
  15. Attention: This template ({{cite pmid}}) is deprecated. To cite the publication identified by PMID 22133323, please use {{cite journal}} with |pmid=22133323 instead.
  16. Asnangkornchai, S (2005). "Kratom Plant in Thai society; culture, behavior". Health Science Laws. {{cite journal}}: |access-date= requires |url= (help); Unknown parameter |coauthors= ignored (|author= suggested) (help)
  17. "Seizure and coma following Kratom (Mitragynina speciosa Korth) exposure". Journal of Medical Toxicology. 6 (4): 424–426. 2010. doi:10.1007/s13181-010-0079-5. PMID 20411370. {{cite journal}}: Unknown parameter |authors= ignored (help)
  18. "Kratom alkaloids and O-desmethyltramadol in urine of a "Krypton" herbal mixture consumer". Forensic Science International. 208 (1–3): 47–52. 2011. doi:10.1016/j.forsciint.2010.10.025. PMID 21112167. {{cite journal}}: Unknown parameter |authors= ignored (help)
  19. "Krypton—new, deadly Internet drug". Lakartidningen (in Swedish). 107 (50): 3196–3197. 2010. PMID 21294331. {{cite journal}}: Unknown parameter |authors= ignored (help)
  20. "Unintentional fatal intoxications with mitragynine and O-desmethyltramadol from the herbal blend Krypton, which is altered kratom and should not be confused with kratom". Journal of Analytical Toxicology. 35 (4): 242–247. 2011. PMID 21513619. {{cite journal}}: Unknown parameter |authors= ignored (help)
  21. "Intrahepatic cholestasis following abuse of powdered kratom (Mitragyna speciosa)". Journal of Medicinal Toxicology. 7 (3): 227–231. 2011. doi:10.1007/s13181-011-0155-5. PMID 21528385. {{cite journal}}: Unknown parameter |authors= ignored (help)
  22. "Mitragyna speciosa, a psychoactive tree from Southeast Asia with opioid activity". Current Topics in Medicinal Chemistry. 11: 1165–1175. 2011. doi:10.2174/156802611795371305. PMID 21050173. {{cite journal}}: Unknown parameter |authors= ignored (help)
  23. Dayer, P; Desmeules, J; Collart, L (1997). "Pharmacology of tramadol". Drugs. 53 (Suppl 2): 18–24. doi:10.2165/00003495-199700532-00006. PMID 9190321.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  24. Musshoff, F., and B. Madea. (2001). "Fatality due to ingestion of tramadol alone". Forensic Science International. 116 (6): 197–199. {{cite journal}}: Unknown parameter |month= ignored (help)CS1 maint: multiple names: authors list (link)
  25. Suwanlert, Sangun (1975). "A Study of Kratom Eaters in Thailand". Bulletin on Narcotics. 27 (3): 21–27. {{cite journal}}: |access-date= requires |url= (help)
  26. Jansen, Karl L.R. (1988-01-04). "Ethnopharmacology of Kratom and the Mitragyna Alkaloids". Journal of Ethnophamacology. 23 (1): 115–119. ISSN 0378-8741. PMID 3419199. {{cite journal}}: |access-date= requires |url= (help); Unknown parameter |coauthors= ignored (|author= suggested) (help)
  27. Reanmongkol, Wantana (March 2007). "Effects of the extracts from Mitragyna speciosa Korth. leaves on analgesic and behavioral activities in experimental animals" (PDF). Songklanakarin Journal of Science and Technology. 29 (1): 39–48. Retrieved 2012-10-26. {{cite journal}}: Unknown parameter |coauthors= ignored (|author= suggested) (help)
  28. Wink, Michael; Roberts, M. W. (1998). Alkaloids: biochemistry, ecology, and medicinal applications. New York: Plenum Press. ISBN 0-306-45465-3.{{cite book}}: CS1 maint: multiple names: authors list (link)
  29. "'Groovy new drug' Kratom gaining in popularity - and perfectly legal". KBOI. 2013-03-06. Retrieved 2013-03-06. {{cite news}}: |first= missing |last= (help); Missing pipe in: |first= (help)
  30. Saunders, Hannah (2013-04-04). "Enhanced Kratom: The next big drug". WZZM13. Retrieved 2013-03-05.
  31. "Kelso police restrain naked woman carrying an infant, swinging a hammer". TDN. 2013-04-03. Retrieved 2013-03-05. {{cite news}}: |first= missing |last= (help)
  32. Cassuto, Dan (2013-04-04). "100% natural, 100% potent, 110% party' but possibly dangerous". KATU. Retrieved 2013-03-05.
  33. Kratom as a Drug and Chemical of Concern
  34. Indiana HB1196
  35. Remove Mitragynine & 7-hydroxymitragynine from Indiana's HB 1196! Save Kratom from prohibition! Change.org.
  36. Iowa SF2341
  37. Kiley, Brendan (2012-04-10). "The Rush to Prohibit Kratom". The Stranger. Retrieved 2012-10-30.
  38. Louisiana SB130
  39. Massachusetts H526

Further reading

  • Mitragynine on ToxNet CASRN: 4098-40-2
  • K. M. Babu, Ch. R. McCurdy, E.W. Boyer: Opioid receptors and legal highs: Salvia divinorum and Kratom, Clinical Toxicology * 46, 146-152
  • E.W. Boyer, K. M. Babu, G. E. Macalino, W. Compton, Self-Treatment of Opioid With-drawal with a Dietary Supplement, Kratom, The American Journal on Addictions, 16: 352-356, 2007
  • E.W. Boyer, K. M. Babu, J. E. Adkins, Ch. R. McCurdy, J. H. Halpern, Self-treatment of opioid withdrawal using kratom (Mitragynia speciosa korth), Addiction, 103 *. 1048-1050, 2008
  • European Monitoring Centre for Drugs and Drug Addiction. "Kratom (Mitragyna speciosa)". Retrieved 2013-03-08. {{cite journal}}: Cite journal requires |journal= (help)
  • K. S. Grewal, Observations on the pharmacology of mitragynine, J Pharmacology and Experimental Therapeutics 1932, 46:251-71 und K. S. Grewal, The Effect of Mitragynine on Man, British Journal of Medical Psychology 1932, 12: 41-58
  • http://www.usdoj.gov/dea/programs/forensicsci/microgram/mg0306/mg0306.pdf
  • S. Suwanlert, A study of kratom eaters in Thailand, UNODC – Bulletin on Narcotics Vol. 27*: 21-27, 1975
  • Jansen, Prast Psychoactive properties of mitragynine (kratom), Journal of Psychoactive Drugs 1988, 20*-457
  • Hiromitsu Takayama: Chemistry and Pharmacology of Analgetic Indole Alkaloids from the Rubiaceous Plant, Mitragyna speciosa; Review; Chem. Pharm. Bull. 52* 916-928 *
  • Suchitra Thongpradichote, et al.: Identification of opioid receptor subtypes in antino-ciceptive actions of supraspinally-administered mitragynine in mice; Life Sciences, Vol. 62, No. 16, Seite 1371-1378, 1998
  • UNITED NATIONS OFFICE ON DRUGS AND CRIME, Vienna, BULLETIN ON NARCOTICS, Volume LVII, Nos. 1 and 2, 2005, S. 249-256, UNITED NATIONS New York, 2007
  • Aekajit Chaiyawong: "Drugs Situation and the Drugs Information System in Thailand", Global Workshop on Drug Information Systems: Activities, Methods and Future Oppor-tunities, Wien, 3.-5. Dezember 2001, unterstützt durch das "United Nations International Drug Control Programme under the Global Assessment Programme on Drug Abuse" (GAP). United Nations, New York, 2002, Weitere Informationen sind auf der GAP Inter-netseite www.undcp.org zu finden.

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