Cargando…

Physiological and pharmacokinetic effects of oral 1,3-dimethylamylamine administration in men

BACKGROUND: 1,3-dimethylamylamine (DMAA) has been a component of dietary supplements and is also used within "party pills," often in conjunction with alcohol and other drugs. Ingestion of higher than recommended doses results in untoward effects including cerebral hemorrhage. To our knowle...

Descripción completa

Detalles Bibliográficos
Autores principales: Schilling, Brian K, Hammond, Kelley G, Bloomer, Richard J, Presley, Chaela S, Yates, Charles R
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3852303/
https://www.ncbi.nlm.nih.gov/pubmed/24090077
http://dx.doi.org/10.1186/2050-6511-14-52
_version_ 1782478645862858752
author Schilling, Brian K
Hammond, Kelley G
Bloomer, Richard J
Presley, Chaela S
Yates, Charles R
author_facet Schilling, Brian K
Hammond, Kelley G
Bloomer, Richard J
Presley, Chaela S
Yates, Charles R
author_sort Schilling, Brian K
collection PubMed
description BACKGROUND: 1,3-dimethylamylamine (DMAA) has been a component of dietary supplements and is also used within "party pills," often in conjunction with alcohol and other drugs. Ingestion of higher than recommended doses results in untoward effects including cerebral hemorrhage. To our knowledge, no studies have been conducted to determine both the pharmacokinetic profile and physiologic responses of DMAA. METHODS: Eight men reported to the lab in the morning following an overnight fast and received a single 25 mg oral dose of DMAA. Blood samples were collected before and through 24 hours post-DMAA ingestion and analyzed for plasma DMAA concentration using high-performance liquid chromatography–mass spectrometry. Resting heart rate, blood pressure, and body temperature was also measured. RESULTS: One subject was excluded from the data analysis due to abnormal DMAA levels. Analysis of the remaining seven participants showed DMAA had an oral clearance of 20.02 ± 5 L∙hr(-1), an oral volume of distribution of 236 ± 38 L, and terminal half-life of 8.45 ± 1.9 hr. Lag time, the delay in appearance of DMAA in the circulation following extravascular administration, varied among participants but averaged approximately 8 minutes (0.14 ± 0.13 hr). The peak DMAA concentration for all subjects was observed within 3–5 hours following ingestion and was very similar across subjects, with a mean of ~70 ng∙mL(-1). Heart rate, blood pressure, and body temperature were largely unaffected by DMAA treatment. CONCLUSIONS: These are the first data to characterize the oral pharmacokinetic profile of DMAA. These findings indicate a consistent pattern of increase across subjects with regards to peak DMAA concentration, with peak values approximately 15–30 times lower than those reported in case studies linking DMAA intake with adverse events. Finally, a single 25 mg dose of DMAA does not meaningfully impact resting heart rate, blood pressure, or body temperature. TRIAL REGISTRATION: NCT01765933
format Online
Article
Text
id pubmed-3852303
institution National Center for Biotechnology Information
language English
publishDate 2013
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-38523032013-12-06 Physiological and pharmacokinetic effects of oral 1,3-dimethylamylamine administration in men Schilling, Brian K Hammond, Kelley G Bloomer, Richard J Presley, Chaela S Yates, Charles R BMC Pharmacol Toxicol Research Article BACKGROUND: 1,3-dimethylamylamine (DMAA) has been a component of dietary supplements and is also used within "party pills," often in conjunction with alcohol and other drugs. Ingestion of higher than recommended doses results in untoward effects including cerebral hemorrhage. To our knowledge, no studies have been conducted to determine both the pharmacokinetic profile and physiologic responses of DMAA. METHODS: Eight men reported to the lab in the morning following an overnight fast and received a single 25 mg oral dose of DMAA. Blood samples were collected before and through 24 hours post-DMAA ingestion and analyzed for plasma DMAA concentration using high-performance liquid chromatography–mass spectrometry. Resting heart rate, blood pressure, and body temperature was also measured. RESULTS: One subject was excluded from the data analysis due to abnormal DMAA levels. Analysis of the remaining seven participants showed DMAA had an oral clearance of 20.02 ± 5 L∙hr(-1), an oral volume of distribution of 236 ± 38 L, and terminal half-life of 8.45 ± 1.9 hr. Lag time, the delay in appearance of DMAA in the circulation following extravascular administration, varied among participants but averaged approximately 8 minutes (0.14 ± 0.13 hr). The peak DMAA concentration for all subjects was observed within 3–5 hours following ingestion and was very similar across subjects, with a mean of ~70 ng∙mL(-1). Heart rate, blood pressure, and body temperature were largely unaffected by DMAA treatment. CONCLUSIONS: These are the first data to characterize the oral pharmacokinetic profile of DMAA. These findings indicate a consistent pattern of increase across subjects with regards to peak DMAA concentration, with peak values approximately 15–30 times lower than those reported in case studies linking DMAA intake with adverse events. Finally, a single 25 mg dose of DMAA does not meaningfully impact resting heart rate, blood pressure, or body temperature. TRIAL REGISTRATION: NCT01765933 BioMed Central 2013-10-04 /pmc/articles/PMC3852303/ /pubmed/24090077 http://dx.doi.org/10.1186/2050-6511-14-52 Text en Copyright © 2013 Schilling et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Schilling, Brian K
Hammond, Kelley G
Bloomer, Richard J
Presley, Chaela S
Yates, Charles R
Physiological and pharmacokinetic effects of oral 1,3-dimethylamylamine administration in men
title Physiological and pharmacokinetic effects of oral 1,3-dimethylamylamine administration in men
title_full Physiological and pharmacokinetic effects of oral 1,3-dimethylamylamine administration in men
title_fullStr Physiological and pharmacokinetic effects of oral 1,3-dimethylamylamine administration in men
title_full_unstemmed Physiological and pharmacokinetic effects of oral 1,3-dimethylamylamine administration in men
title_short Physiological and pharmacokinetic effects of oral 1,3-dimethylamylamine administration in men
title_sort physiological and pharmacokinetic effects of oral 1,3-dimethylamylamine administration in men
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3852303/
https://www.ncbi.nlm.nih.gov/pubmed/24090077
http://dx.doi.org/10.1186/2050-6511-14-52
work_keys_str_mv AT schillingbriank physiologicalandpharmacokineticeffectsoforal13dimethylamylamineadministrationinmen
AT hammondkelleyg physiologicalandpharmacokineticeffectsoforal13dimethylamylamineadministrationinmen
AT bloomerrichardj physiologicalandpharmacokineticeffectsoforal13dimethylamylamineadministrationinmen
AT presleychaelas physiologicalandpharmacokineticeffectsoforal13dimethylamylamineadministrationinmen
AT yatescharlesr physiologicalandpharmacokineticeffectsoforal13dimethylamylamineadministrationinmen