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

BMC Pharmacol Toxicol

Department of Health and Sport Sciences, The University of Memphis, 161 Roane Fieldhouse, 38152 Memphis, TN, USA.

Published: October 2013

AI Article Synopsis

  • DMAA (1,3-dimethylamylamine) is often found in dietary supplements and "party pills," linked to severe side effects like cerebral hemorrhage from high doses, yet no existing studies have analyzed its pharmacokinetics or physiological effects.
  • In a study with eight men, participants ingested a single 25 mg dose of DMAA, and data were collected on blood plasma levels, heart rate, blood pressure, and body temperature over 24 hours.
  • Results showed a clear pharmacokinetic profile for DMAA, with a peak concentration appearing 3-5 hours post-ingestion but found no significant changes in heart rate, blood pressure, or body temperature, indicating that low doses may not have major

Article Abstract

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.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3852303PMC
http://dx.doi.org/10.1186/2050-6511-14-52DOI Listing

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