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Pharmacokinetics of mitragynine in man

BACKGROUND: Kratom, known botanically as Mitragyna speciosa (Korth.), is an indigenous tree in Southeast Asia. Kratom is currently easily available worldwide via special shops and the Internet to use as a drug of abuse, opioid alternative, or pain killer. So far, the pharmacokinetics of this plant h...

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Autores principales: Trakulsrichai, Satariya, Sathirakul, Korbtham, Auparakkitanon, Saranya, Krongvorakul, Jatupon, Sueajai, Jetjamnong, Noumjad, Nantida, Sukasem, Chonlaphat, Wananukul, Winai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4425236/
https://www.ncbi.nlm.nih.gov/pubmed/25995615
http://dx.doi.org/10.2147/DDDT.S79658
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author Trakulsrichai, Satariya
Sathirakul, Korbtham
Auparakkitanon, Saranya
Krongvorakul, Jatupon
Sueajai, Jetjamnong
Noumjad, Nantida
Sukasem, Chonlaphat
Wananukul, Winai
author_facet Trakulsrichai, Satariya
Sathirakul, Korbtham
Auparakkitanon, Saranya
Krongvorakul, Jatupon
Sueajai, Jetjamnong
Noumjad, Nantida
Sukasem, Chonlaphat
Wananukul, Winai
author_sort Trakulsrichai, Satariya
collection PubMed
description BACKGROUND: Kratom, known botanically as Mitragyna speciosa (Korth.), is an indigenous tree in Southeast Asia. Kratom is currently easily available worldwide via special shops and the Internet to use as a drug of abuse, opioid alternative, or pain killer. So far, the pharmacokinetics of this plant has been studied only in animals, and there is no such study in humans. The major abundant active alkaloid in Kratom, mitragynine, is one of the promising new chemical substances to be developed as a new drug. The aim of this study was to examine the pharmacokinetics of mitragynine and assess the linearity in pharmacokinetics in chronic users. METHODS: Since Kratom is illegal in Thailand, studies in healthy subjects would be unethical. We therefore conducted a prospective study by enrolling ten chronic, regular, healthy users. We adjusted the steady state in each subject by giving a known amount of Kratom tea for 7 days before commencement of the experiment. We admitted and gave different oral doses to subjects to confirm linearity in pharmacokinetics. The mitragynine blood concentrations at 17 times points and the urine concentrations during the 24-hour period were collected and measured by liquid chromatography-tandem mass spectrometry method. RESULTS: Ten male subjects completed the study without adverse reactions. The median duration of abuse was 1.75 years. We analyzed one subject separately due to the abnormal behavior of blood concentration. From data of nine subjects, the pharmacokinetic parameters established were time to reach the maximum plasma concentration (0.83±0.35 hour), terminal half-life (23.24±16.07 hours), and the apparent volume of distribution (38.04±24.32 L/kg). The urine excretion of unchanged form was 0.14%. The pharmacokinetics were observed to be oral two-compartment model. CONCLUSION: This was the first pharmacokinetic study in humans, which demonstrated linearity and was consistent with the oral two-compartment model with a terminal half-life of about 1 day. The pharmacokinetic linearity and parameters reported are necessary pharmacological information of Kratom, and there is a possibility for it to be developed medically as a pain killer or better opioid substitute in the future.
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spelling pubmed-44252362015-05-20 Pharmacokinetics of mitragynine in man Trakulsrichai, Satariya Sathirakul, Korbtham Auparakkitanon, Saranya Krongvorakul, Jatupon Sueajai, Jetjamnong Noumjad, Nantida Sukasem, Chonlaphat Wananukul, Winai Drug Des Devel Ther Original Research BACKGROUND: Kratom, known botanically as Mitragyna speciosa (Korth.), is an indigenous tree in Southeast Asia. Kratom is currently easily available worldwide via special shops and the Internet to use as a drug of abuse, opioid alternative, or pain killer. So far, the pharmacokinetics of this plant has been studied only in animals, and there is no such study in humans. The major abundant active alkaloid in Kratom, mitragynine, is one of the promising new chemical substances to be developed as a new drug. The aim of this study was to examine the pharmacokinetics of mitragynine and assess the linearity in pharmacokinetics in chronic users. METHODS: Since Kratom is illegal in Thailand, studies in healthy subjects would be unethical. We therefore conducted a prospective study by enrolling ten chronic, regular, healthy users. We adjusted the steady state in each subject by giving a known amount of Kratom tea for 7 days before commencement of the experiment. We admitted and gave different oral doses to subjects to confirm linearity in pharmacokinetics. The mitragynine blood concentrations at 17 times points and the urine concentrations during the 24-hour period were collected and measured by liquid chromatography-tandem mass spectrometry method. RESULTS: Ten male subjects completed the study without adverse reactions. The median duration of abuse was 1.75 years. We analyzed one subject separately due to the abnormal behavior of blood concentration. From data of nine subjects, the pharmacokinetic parameters established were time to reach the maximum plasma concentration (0.83±0.35 hour), terminal half-life (23.24±16.07 hours), and the apparent volume of distribution (38.04±24.32 L/kg). The urine excretion of unchanged form was 0.14%. The pharmacokinetics were observed to be oral two-compartment model. CONCLUSION: This was the first pharmacokinetic study in humans, which demonstrated linearity and was consistent with the oral two-compartment model with a terminal half-life of about 1 day. The pharmacokinetic linearity and parameters reported are necessary pharmacological information of Kratom, and there is a possibility for it to be developed medically as a pain killer or better opioid substitute in the future. Dove Medical Press 2015-04-29 /pmc/articles/PMC4425236/ /pubmed/25995615 http://dx.doi.org/10.2147/DDDT.S79658 Text en © 2015 Trakulsrichai et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Trakulsrichai, Satariya
Sathirakul, Korbtham
Auparakkitanon, Saranya
Krongvorakul, Jatupon
Sueajai, Jetjamnong
Noumjad, Nantida
Sukasem, Chonlaphat
Wananukul, Winai
Pharmacokinetics of mitragynine in man
title Pharmacokinetics of mitragynine in man
title_full Pharmacokinetics of mitragynine in man
title_fullStr Pharmacokinetics of mitragynine in man
title_full_unstemmed Pharmacokinetics of mitragynine in man
title_short Pharmacokinetics of mitragynine in man
title_sort pharmacokinetics of mitragynine in man
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4425236/
https://www.ncbi.nlm.nih.gov/pubmed/25995615
http://dx.doi.org/10.2147/DDDT.S79658
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