Literature DB >> 20406628

Combined treatment with MAO-A inhibitor and MAO-B inhibitor increases extracellular noradrenaline levels more than MAO-A inhibitor alone through increases in beta-phenylethylamine.

Yuji Kitaichi1, Takeshi Inoue, Shin Nakagawa, Shuken Boku, Takeshi Izumi, Tsukasa Koyama.   

Abstract

Monoamine oxidase inhibitors (MAO inhibitors) have been widely used as antidepressants. However, it remains unclear whether a difference exists between non-selective MAO inhibitors and selective MAO-A inhibitors in terms of their antidepressant effects. Using in vivo microdialysis methods, we measured extracellular noradrenaline and serotonin levels following administration of Ro 41-1049, a reversible MAO-A inhibitor and/or lazabemide, a reversible MAO-B inhibitor in the medial prefrontal cortex (mPFC) of rats. We examined the effect of local infusion of beta-phenylethylamine to the mPFC of rats on extracellular noradrenaline and serotonin levels. Furthermore, the concentrations of beta-phenylethylamine in the tissue of the mPFC after combined treatment with Ro 41-1049 and lazabemide were measured. The Ro 41-1049 alone and the combined treatment significantly increased extracellular noradrenaline levels compared with vehicle and lazabemide alone. Furthermore, the combined treatment increased noradrenaline levels significantly more than Ro 41-1049 alone did. The Ro 41-1049 alone and the combined treatment significantly increased extracellular serotonin levels compared with vehicle and lazabemide alone, but no difference in serotonin levels was found between the combined treatment group and the Ro 41-1049 group. Local infusion of low-dose beta-phenylethylamine increased extracellular noradrenaline levels, but not that of serotonin. Only the combined treatment significantly increased beta-phenylethylamine levels in tissues of the mPFC. Our results suggest that the combined treatment with a MAO-A inhibitor and a MAO-B inhibitor strengthens antidepressant effects because the combined treatment increases extracellular noradrenaline levels more than a MAO-A inhibitor alone through increases in beta-phenylethylamine. Copyright 2010 Elsevier B.V. All rights reserved.

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Year:  2010        PMID: 20406628     DOI: 10.1016/j.ejphar.2010.04.014

Source DB:  PubMed          Journal:  Eur J Pharmacol        ISSN: 0014-2999            Impact factor:   4.432


  5 in total

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Journal:  Front Psychol       Date:  2011-07-07

3.  An adrenal mass and increased catecholamines: monoamine oxidase or pheochromocytoma effect?

Authors:  Marianne R F Bosscher; Iris M Wentholt; Mariette T Ackermans; Els J M Nieveen van Dijkum
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4.  Perseveration in a spatial-discrimination serial reversal learning task is differentially affected by MAO-A and MAO-B inhibition and associated with reduced anxiety and peripheral serotonin levels.

Authors:  Peter Zhukovsky; Johan Alsiö; Bianca Jupp; Jing Xia; Chiara Giuliano; Lucy Jenner; Jessica Griffiths; Errin Riley; Sajeed Ali; Angela C Roberts; Trevor W Robbins; Jeffrey W Dalley
Journal:  Psychopharmacology (Berl)       Date:  2017-03-02       Impact factor: 4.530

5.  Xanthoangelol and 4-Hydroxyderricin Are the Major Active Principles of the Inhibitory Activities against Monoamine Oxidases on Angelica keiskei K.

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Journal:  Biomol Ther (Seoul)       Date:  2013-05-30       Impact factor: 4.634

  5 in total

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