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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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Analysis of the monoamine oxidase A (MAOA) gene in bipolar affective disorder by association studies, meta-analyses, and sequencing of the promoter.

TL;DR: Positive associations of the monoamine oxidase A (MAOA) gene with bipolar affective disorder and a novel polymorphic promoter variable number of tandem repeats (VNTR) located approximately 1,200 bp upstream from the translation start site suggest that there may be functional variants in other regions of the MAOA gene or neighbouring genes that affect bipolar Affective disorder risk.
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The psychopharmacology of aggressive behavior: a translational approach: part 2: clinical studies using atypical antipsychotics, anticonvulsants, and lithium.

TL;DR: A critical review of all clinical trials using atypical antipsychotics, anticonvulsants, and lithium shows that a multifunctional combined therapy, targeting different receptors, seems to be the best strategy for treating aggressive behavior.
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Determinants of regional and local diversity within the astroglial lineage of the normal central nervous system.

TL;DR: A review of the evidence for and mechanistic determinants of regional and local astrocyte diversity can be found in this paper, where it is shown that many phenotypic traits of the non-neuronal glial cells are responsive to local environmental cues (i.e., are adaptable), suggesting that plasticity contributes to this diversity.
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Origins of antisocial behavior: negative reinforcement and affect dysregulation of behavior as socialization mechanisms in family interaction

TL;DR: The authors found that negative reinforcement of aggression and affect dysregulation during family interaction may play complementary roles in the development of antisocial behavior by fostering the use of coercive means of dealing with social conflict.
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Association analysis of the functional monoamine oxidase A gene promoter polymorphism in psychiatric disorders.

TL;DR: There is no association between MAOA-LPR genotype and susceptibility to recurrent major depression, bipolar disorder, and schizophrenia in the population of patients tested.
References
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Journal Article

Behavioral despair in mice: a primary screening test for antidepressants

TL;DR: The mouse procedure is more rapid and less costly than that with rats and is thus more suitable for the primary screening of antidepressant drugs, suggesting that the procedure is selectively sensitive to antidepressant treatments.
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Functional role of type I and type II interferons in antiviral defense.

TL;DR: Comparison of mice lacking either type I or type II IFN receptors showed that, at least in response to some viruses, both IFN systems are essential for antiviral defense and are functionally nonredundant.
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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.

TL;DR: The author describes how his methods of investigation with celloidin embedded material prepared with the Golgi method and Nissl staining revealed for the first time the “barrel fields” of the mouse cerebral cortex that are activated by stimulation of the facial vibrissae (whiskers).
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Genetic Applications of an Inverse Polymerase Chain Reaction

TL;DR: The feasibility of IPCR is shown by amplifying the sequences that flank an IS1 element in the genome of a natural isolate of Escherichia coli.
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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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