Literature DB >> 26086546

Androgen metabolites impact CSF amines and axonal serotonin via MAO-A and -B in male macaques.

C L Bethea1, K Phu2, A Kim2, A P Reddy2.   

Abstract

A number of studies have shown that mutations or deletions of the monoamine oxidase-A (MAO-A) gene cause elevated CNS serotonin and elevated impulsive aggression in humans and animal models. In addition, low cerebrospinal fluid (CSF) 5-hydroxyindole acetic acid (5HIAA) has been documented in a limited number of violent criminal populations and in macaques that exhibit impulsive aggression. To reconcile these different analyses, we hypothesized that CSF 5HIAA reflected degradation of serotonin by the activity of MAO-A; and that low MAO-A activity would result in lower CSF 5HIAA, but overall higher serotonin in the CNS. To test this hypothesis, male Japanese macaques (Macaca fuscata) were castrated, rested for 5-7months, and then treated for 3months with [1] placebo, [2] testosterone (T), [3] dihydrotestosterone (DHT; non-aromatizable androgen) and 1,4,6-androstatriene-3,17-dione (ATD) (steroidal aromatase inhibitor), or [4] flutamide (FLUT; androgen antagonist) and ATD (n=5/group). These treatments enable isolation of androgen and estrogen activities. In the dorsal raphe, MAO-A and MAO-B expressions were determined with in situ hybridization (ISH) and protein expression of aromatase was determined with immunohistochemistry (IHC). CSF concentrations of 5HIAA, 3-methoxy-4-hydroxyphenylglycol (MHPG), and homovanillic acid (HVA) were determined with liquid chromatography/mass spectrometry (LC/MS). From the same animals, previously published data on serotonin axon density were used as a proxy for CNS serotonin. Aromatase conversion of T to estrogen (E) suppressed MAO-A (positive pixel area, p=0.0045), but androgens increased MAO-B (positive pixel area, p=0.014). CSF 5HIAA was suppressed by conversion of T to E (Cohen's d=0.6). CSF 5HIAA was positively correlated with MAO-A-positive pixel area (r(2)=0.78). CSF 5HIAA was inversely correlated with serotonin axon-positive pixel area (r(2)=0.69). In summary, CSF 5HIAA reflects MAO-A activity rather than global serotonin. Low CSF 5HIAA may, in this paradigm, reflect higher serotonin activity. Androgens lower MAO-A activity via metabolism to E, thus elevating CNS serotonin and decreasing CSF 5HIAA. Since androgens increase certain types of aggression, these data are consistent with studies demonstrating that lower MAO-A activity is associated with elevated serotonin and increased aggression.
Copyright © 2015 IBRO. Published by Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  CSF 5HIAA; MAO-A; MAO-B; aromatase; male; serotonin

Mesh:

Substances:

Year:  2015        PMID: 26086546      PMCID: PMC4520442          DOI: 10.1016/j.neuroscience.2015.06.020

Source DB:  PubMed          Journal:  Neuroscience        ISSN: 0306-4522            Impact factor:   3.590


  76 in total

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Review 3.  The effectiveness of antidepressant medication in the management of behaviour problems in adults with intellectual disabilities: a systematic review.

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4.  Oestradiol modulation of serotonin reuptake transporter and serotonin metabolism in the brain of monkeys.

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6.  Physical provocation potentiates aggression in male rats receiving anabolic androgenic steroids.

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8.  Differential effects of aromatase inhibition on luteinizing hormone secretion in intact and castrated male cynomolgus macaques.

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9.  Reversal of testosterone-induced dominance by the serotonergic agonist quipazine.

Authors:  K R Bonson; J C Winter
Journal:  Pharmacol Biochem Behav       Date:  1992-08       Impact factor: 3.533

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Authors:  Amy L Byrd; Stephen B Manuck
Journal:  Biol Psychiatry       Date:  2013-06-18       Impact factor: 13.382

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2.  Alzheimer Disease and Selected Risk Factors Disrupt a Co-regulation of Monoamine Oxidase-A/B in the Hippocampus, but Not in the Cortex.

Authors:  Maa O Quartey; Jennifer N K Nyarko; Paul R Pennington; Ryan M Heistad; Paula C Klassen; Glen B Baker; Darrell D Mousseau
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