Research output

Quantification of endogenous neurotransmitters and related compounds by liquid chromatography coupled to tandem mass spectrometry

Research output: Contribution to journalArticleAcademicpeer-review

Associated researcher

  • Olesti, E.
  • Rodríguez-Morató, J.
  • Gomez-Gomez, A.
  • Ramaekers, J.G.

  • de la Torre, R.
  • Pozo, O. J.

Associated organisations

Abstract

Neurotransmitters are signaling molecules, playing key roles in neuronal communications in the brain. Drug induced changes in neurotransmitters and other brain metabolite concentration may be used to characterize drugs according to their targeted metabolomics profile. Here, we report the development and validation of a straightforward liquid chromatography-tandem mass spectrometry (LC-MS/MS) method for the simultaneous quantification of 16 endogenous small polar compounds in rat plasma and brain homogenates. The method enables the quantification of the neurotransmitters γ-aminobutyric acid, glutamate, acetylcholine and adenosine, as well as choline, glutamine, acetylcarnitine, carnitine, creatine, creatinine, valine, leucine, isoleucine, phenylalanine, tyrosine and tryptophan. After optimizing the sample preparation, chromatographic and spectrometric conditions, the method was successfully validated using the standard addition approach and a hydrophilic interaction chromatography (HILIC) with an amide column. The method was shown to be linear (r > 0.99) as all the compounds were within the ±25% values of intra and inter-day precision and accuracy acceptance. A matrix effect was corrected with the use of 10 isotopically labelled internal standards and the compound stability was evaluated for all compounds. Relevant exaltation of choline (in plasma) and creatinine (in brain) were solved with -20 °C conditions. The applicability of the method was tested by evaluating brain alterations in the concentrations of neurotransmitters and related compounds after the administration of two psychostimulant drugs of abuse (cocaine and methylenedioxypyrovalerone) to rats. A neuro-metabolic fingerprint of each drug was obtained that reflected their pharmacological profile. Altogether, this methodology presents a valuable targeted metabolomics tool for basic and clinical research studies.

    Research areas

  • 3,4-METHYLENEDIOXYPYROVALERONE MDPV, AMINO-ACID, BATH SALTS, BRAIN-TISSUE, Brain neurotransmitters, Hydrophilic interaction chromatography, Liquid chromatography coupled to mass spectrometry, METABOLITES, MICROEXTRACTION, MONOAMINE NEUROTRANSMITTERS, Psychoactive substances, Quantitative method, RAT-BRAIN, Standard addition, TOXICOLOGY, UHPLC-MS/MS
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Details

Original languageEnglish
Pages (from-to)93-102
Number of pages10
JournalTalanta
Volume192
DOIs
Publication statusPublished - 15 Jan 2019