Metabolomics of Rat Brain After Treatment with Phenelzine: High-Resolution Mass Spectrometric Demonstration of Increased Brain Levels of N-Acetyl Amino Acids

Author Info

Paul L. Wood John E. Cebak Glen B. Baker

Corresponding Author

Paul L. Wood
Metabolomics Unit, College of Veterinary Medicine, Lincoln Memorial University, Tennessee, USA

A B S T R A C T

Background: Phenelzine (PLZ) is a non-specific monoamine oxidase inhibitor that has demonstrated clinical efficacy in patients with treatment resistant depression. The mechanism of action with regard to this efficacy is complicated in that its metabolite, β-phenylethylidenehydrazine (PEH), is an inhibitor of amino acid transaminases resulting in dramatic brain elevations of GABA, alanine, ornithine and tyrosine. The full neurochemical profile of PLZ and PEH remain to be explored. Objective: To undertake a non-targeted metabolomics study of phenelzine on rat brain neurochemistry. Methods: We undertook a high-resolution mass spectrometric metabolomics analysis of rat cortical brain 1 and 12 hours after intraperitoneal dosing with PLZ or PEH. Tandem mass spectrometry was utilized to obtain relative quantitation data. Results: N-acetyl amino acids were found to be elevated in cortical brain tissue following either PLZ or PEH treatments. Conclusions: Our data indicate PLZ treatment significantly augments brain levels of N-acetyl amino acids and that this may involve inhibition of deacylases by PEH and/or induction of N-amino acid acetyltransferases.

Article Info

Article Type

Research Article

Publication history

Received: Sat 20, Jun 2020
Accepted: Tue 07, Jul 2020
Published: Fri 24, Jul 2020

Copyright

© 2023 Paul L. Wood. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Hosting by Science Repository.
DOI: 10.31487/j.NNB.2020.03.03