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Open AccessJournal ArticleDOI

Aggressive Behavior and Altered Amounts of Brain Serotonin and Norepinephrine in Mice Lacking MAOA

TLDR
Pup behavioral alterations, including trembling, difficulty in righting, and fearfulness were reversed by the serotonin synthesis inhibitor parachlorophenylalanine, and adults manifested a distinct behavioral syndrome, including enhanced aggression in males.
Abstract
Deficiency in monoamine oxidase A (MAOA), an enzyme that degrades serotonin and norepinephrine, has recently been shown to be associated with aggressive behavior in men of a Dutch family. A line of transgenic mice was isolated in which transgene integration caused a deletion in the gene encoding MAOA, providing an animal model of MAOA deficiency. In pup brains, serotonin concentrations were increased up to ninefold, and serotonin-like immunoreactivity was present in catecholaminergic neurons. In pup and adult brains, norepinephrine concentrations were increased up to twofold, and cytoarchitectural changes were observed in the somatosensory cortex. Pup behavioral alterations, including trembling, difficulty in righting, and fearfulness were reversed by the serotonin synthesis inhibitor parachlorophenylalanine. Adults manifested a distinct behavioral syndrome, including enhanced aggression in males.

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Reduced activity of monoamine oxidase in the rat brain following repeated nandrolone decanoate administration.

TL;DR: The reduced MAO activities observed are in line with the previously presented findings of decreased extracellular levels of DOPAC and HVA in the rat brain, indicating decreased monoaminergic activity following repeated AAS administration.
Journal ArticleDOI

Insights into enzyme point mutation effect by molecular simulation: phenylethylamine oxidation catalyzed by monoamine oxidase A

TL;DR: The I335Y point mutation effect on the kinetics of phenylethylamine decomposition catalyzed by monoamine oxidase A was elucidated by means of molecular simulation and a major change in the interaction between phenyl rings of the substrate and the neighboring Phe352 residue is revealed due to the increased local polarity.
Journal ArticleDOI

Desarrollo del comportamiento antisocial: factores psicobiológicos, ambientales e interacciones genotipo-ambiente

TL;DR: For instance, a recent study as mentioned in this paper showed that the existence of a mecanismos fisiologicos that can be modulado with respect to factores ambientales and geneticos, e.g., the monoaminooxidasa A (MAOA) gene, which is associated with comportamiento antisocial.
Journal ArticleDOI

Serotonin levels are abnormally elevated in the fetus of the monoamine oxidase-A-deficient transgenic mouse

TL;DR: The results indicated that the absence of monoamine oxidase A activity in Tg8 mice results in abnormally high 5-hydroxytryptamine (5-HT) levels in all the central nervous structures and at all the studied developmental ages.
Book ChapterDOI

Development of thalamocortical projections in normal and mutant mice.

TL;DR: The number of available mutants is increasing rapidly and, combined with recent technology allowing gene expression to be experimentally manipulated in precise spatiotemporal patterns, will provide further understanding of the development and plasticity of thalamocortical connections.
References
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Behavioral despair in mice: a primary screening test for antidepressants

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The structural organization of layer IV in the somatosensory region (SI) of mouse cerebral cortex. The description of a cortical field composed of discrete cytoarchitectonic units.

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Genetic Applications of an Inverse Polymerase Chain Reaction

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Abnormal behavior associated with a point mutation in the structural gene for monoamine oxidase A

TL;DR: Analytical results indicate that isolated complete MAOA deficiency in this family is associated with a recognizable behavioral phenotype that includes disturbed regulation of impulsive aggression.
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