Abstract

The fungal glycoprotein l-lysine α-oxidase (LO) catalyzes the oxidative deamination of l-lysine (l-lys). LO may be internalized in the intestine and shows antitumor, antibacterial, and antiviral effects in vivo. The main mechanisms of its effects have been shown to be depletion of the essential amino acid l-lys and action of reactive oxidative species produced by the reaction. Here, we report that LO penetrates into the brain and is retained there for up to 48 h after intravenous injection, which might be explained by specific pharmacokinetics. LO actively intervenes in amino acid metabolism in the brain. The most significant impact of LO was towards amino acids, which are directly exposed to its action (l-lys, l-orn, l-arg). In addition, the enzyme significantly affected the redistribution of amino acids directly associated with the tricarboxylic acid (TCA) cycle (l-asp and l-glu). We discovered that the depletion of l-orn, the precursor of polyamines (PA), led to a significant and long-term decrease in the concentration of polyamines, which are responsible for regulation of many processes including cell proliferation. Thus, LO may be used to reduce levels of l-lys and PA in the brain.

Highlights

  • The l-lysine (l-lys) is an essential amino acid (AA) for humans

  • Good correspondence of pharmacokinetic parameters determined by direct enzymatic activity measurement and enzyme immunoassay was shown for Escherichia coli (E. coli) l-asparaginase, which is used as a therapeutic [16]

  • The persistence of lysine α-oxidase (LO) in the brain for up to 24 h after i.v. injection is suggested by its exclusion from general metabolism and specific pharmacokinetics in the brain

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Summary

Introduction

The l-lysine (l-lys) is an essential amino acid (AA) for humans. It is used for energy production and the biosynthesis of numerous compounds, including proteins. Nutritional lysine has a sedative (anxiolytic) effect at the level of amygdala and cerebellum, without affecting the heart rate. By this mechanism, food l-lys suppresses artificially induced diarrhea, which is regulated by serotonin [1,2]. L-lys supplementation may represent a new treatment for primary adrenal diseases in which corticosteroid hypersecretion is driven by overexpressed serotonin receptors [3]

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