Target intelligence / Profile preview

Amine oxidase enzyme (AO)

Target
AO
Molecular classification
Enzyme, Oxidoreductase (EC 1.4), Amine oxidase family, Flavin-dependent enzyme (MAOs), Copper-dependent enzyme (CAOs, SSAOs)
01

Overview

Amine oxidase enzymes are a diverse family of oxidoreductases that catalyze the oxidative deamination of primary and secondary amines, including key neurotransmitters and polyamines, producing aldehydes, ammonia, and hydrogen peroxide[3][5]. These enzymes include flavin-dependent monoamine oxidases (MAO-A, MAO-B), copper-dependent amine oxidases (CAO, DAO, SSAO), and the lysyl oxidase (LOX) family[1][3][5][6]. They regulate cellular amine levels, cell adhesion, inflammation, and signaling, and are implicated in diseases such as depression, neurodegeneration, cancer, inflammation, and cardiovascular disorders. Pharmacological inhibition of specific amine oxidases is a therapeutic strategy employed for neuropsychiatric, oncological, and inflammatory indications. Safety concerns arise from adverse metabolic effects of inhibition and the potential for increased oxidative stress[4][5].

Other names
Monoamine oxidase (MAO)Diamine oxidase (DAO)Polyamine oxidaseSemicarbazide-sensitive amine oxidase (SSAO)Copper amine oxidase (CAO)Lysyl oxidase (LOX)Primary-amine oxidase
02

Mechanism of action

Inhibition of oxidative deamination of amines, stabilizing neurotransmitter or polyamine levels (MAOI for depression, Parkinson's); Inhibition of hydrogen peroxide and aldehyde formation (reducing oxidative stress or cell death); Blocking cell adhesion and migration pathways (for vascular inflammation or metastasis, targeting VAP-1/AOC3)

03

Biological functions

Metabolism of biogenic amines (e.g., neurotransmitters, histamine)Regulation of polyamine and monoamine levelsProduction of hydrogen peroxide (H₂O₂)Modulation of cell proliferation and cell deathRegulation of vascular adhesion (e.g., VAP-1/AOC3)Modulation of inflammation and oxidative stress
04

Disease associations

Neurodegenerative disease (especially MAOs, e.g., Parkinson's, depression)Cancer (due to induction of cell death, polyamine metabolism)Inflammation (role in allergic reaction, vascular adhesion)Cardiovascular disease (contribution to oxidative stress, atherosclerosis)Fibrosis (via LOX family)
05

Safety considerations

Risk of serotonin syndrome and hypertensive crisis with MAOIs due to interaction with sympathomimetic drugs or dietary amines (tyramine)Risk of oxidative damage due to excessive hydrogen peroxide formation leading to tissue injuryOff-target effects or broad inhibition may impair normal metabolic functions
06

Interacting drugs

Monoamine oxidase inhibitors (MAOIs; e.g., selegiline, phenelzine, tranylcypromine)

3 more in the full profile.

07

Biomarkers

Expression/activity levels of MAO-A, MAO-B in brain/peripheral tissue for psychiatric and neurodegenerative disordersDAO activity for allergic and inflammatory states (e.g., histamine intolerance)VAP-1/AOC3 levels as marker for vascular inflammationPolyamine oxidase activity/levels in tumors

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