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Biomedical Chromatography
Research article

LC/MS/MS analysis of the endogenous dimethyltryptamine hallucinogens, their precursors, and major metabolites in rat pineal gland microdialysate

Steven A. Barker

Corresponding Author

Department of Comparative Biomedical Sciences, School of Veterinary Medicine, Louisiana State University, Baton Rouge, LA, USA

Correspondence to: S. A. Barker, Department of Comparative Biomedical Sciences, School of Veterinary Medicine, Louisiana State University, Baton Rouge, LA 70803, USA. E‐mail:

sbarker@vetmed.lsu.edu

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Jimo Borjigin

Departments of Molecular & Integrative Physiology1 and Neurology2, University of Michigan Medical School, Ann Arbor, MI, USA

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Izabela Lomnicka

Department of Comparative Biomedical Sciences, School of Veterinary Medicine, Louisiana State University, Baton Rouge, LA, USA

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Rick Strassman

Department of Psychiatry, University of New Mexico School of Medicine, Albuquerque, and Cottonwood Research Foundation, Gallup, New Mexico, USA

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First published: 23 July 2013
Cited by: 11

ABSTRACT

We report a qualitative liquid chromatography–tandem mass spectrometry (LC/MS/MS) method for the simultaneous analysis of the three known N,N‐dimethyltryptamine endogenous hallucinogens, their precursors and metabolites, as well as melatonin and its metabolic precursors. The method was characterized using artificial cerebrospinal fluid (aCSF) as the matrix and was subsequently applied to the analysis of rat brain pineal gland‐aCSF microdialysate. The method describes the simultaneous analysis of 23 chemically diverse compounds plus a deuterated internal standard by direct injection, requiring no dilution or extraction of the samples. The results demonstrate that this is a simple, sensitive, specific and direct approach to the qualitative analysis of these compounds in this matrix. The protocol also employs stringent MS confirmatory criteria for the detection and confirmation of the compounds examined, including exact mass measurements. The excellent limits of detection and broad scope make it a valuable research tool for examining the endogenous hallucinogen pathways in the central nervous system. We report here, for the first time, the presence of N,N‐dimethyltryptamine in pineal gland microdialysate obtained from the rat. Copyright © 2013 John Wiley & Sons, Ltd.

Number of times cited: 11

  • , N,N-dimethyltryptamine and the pineal gland: Separating fact from myth, Journal of Psychopharmacology, 32, 1, (30), (2018).
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  • , Metabolism and urinary disposition of N,N‐dimethyltryptamine after oral and smoked administration: a comparative study, Drug Testing and Analysis, 7, 5, (401-406), (2014).
  • , Noncompetitive Inhibition of Indolethylamine-N-methyltransferase by N,N-Dimethyltryptamine and N,N-Dimethylaminopropyltryptamine, Biochemistry, 53, 18, (2956), (2014).
  • , Biosynthesis of N,N-dimethyltryptamine (DMT) in a melanoma cell line and its metabolization by peroxidases, Biochemical Pharmacology, 88, 3, (393), (2014).
  • , The Therapeutic Potentials of Ayahuasca: Possible Effects against Various Diseases of Civilization, Frontiers in Pharmacology, 10.3389/fphar.2016.00035, 7, (2016).
  • , Novel Psychoactive Substances—Recent Progress on Neuropharmacological Mechanisms of Action for Selected Drugs, Frontiers in Psychiatry, 10.3389/fpsyt.2017.00152, 8, (2017).
  • , Pineal Calcification, Melatonin Production, Aging, Associated Health Consequences and Rejuvenation of the Pineal Gland, Molecules, 10.3390/molecules23020301, 23, 2, (301), (2018).