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Aggression and anxiety: social context and neurobiological links.

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TLDR
Differences in the activity of the hypothalamic–pituitary–adrenal axis, brain arginine vasopressin, and the serotonin systems, among others, which contribute to the distinct behavioural phenotypes related to aggression and anxiety are discussed.
Abstract
Psychopathologies such as anxiety- and depression-related disorders are often characterized by impaired social behaviours including excessive aggression and violence. Excessive aggression and violence likely develop as a consequence of generally disturbed emotional regulation, such as abnormally high or low levels of anxiety. This suggests an overlap between brain circuitries and neurochemical systems regulating aggression and anxiety. In this review, we will discuss different forms of male aggression, rodent models of excessive aggression, and neurobiological mechanisms underlying male aggression in the context of anxiety. We will summarize our attempts to establish an animal model of high and abnormal aggression using rats selected for high (HAB) vs. low (LAB) anxiety-related behaviour. Briefly, male LAB rats and, to a lesser extent, male HAB rats show high and abnormal forms of aggression compared with non-selected (NAB) rats, making them a suitable animal model for studying excessive aggression in the context of extremes in innate anxiety. In addition, we will discuss differences in the activity of the hypothalamic-pituitary-adrenal axis, brain arginine vasopressin, and the serotonin systems, among others, which contribute to the distinct behavioural phenotypes related to aggression and anxiety. Further investigation of the neurobiological systems in animals with distinct anxiety phenotypes might provide valuable information about the link between excessive aggression and disturbed emotional regulation, which is essential for understanding the social and emotional deficits that are characteristic of many human psychiatric disorders.

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Balance of brain oxytocin and vasopressin: implications for anxiety, depression, and social behaviors

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The Oxytocin Receptor: From Intracellular Signaling to Behavior

TL;DR: The mechanisms of OXT expression and release, expression and binding of the OXTR in brain and periphery, OX TR-coupled signaling cascades, and their involvement in behavioral outcomes are discussed to assemble a comprehensive picture of the central and peripheral OXT system.
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Both oxytocin and vasopressin are mediators of maternal care and aggression in rodents: from central release to sites of action.

TL;DR: The functional role of the brain oxytocin and vasopressin system in the context of maternal behavior, specifically maternal care and maternal aggression in rodents is discussed.
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The Neuropeptide Oxytocin Facilitates Pro-Social Behavior and Prevents Social Avoidance in Rats and Mice

TL;DR: The data indicate that the basal activity of the endogenous brain OT system is sufficient to promote natural occurring social preference in rodents while synthetic OT shows potential to reverse stress-induced social avoidance and might thus be of use for treating social phobia and social dysfunction in humans.
References
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Journal ArticleDOI

Impaired repression at a vasopressin promoter polymorphism underlies overexpression of vasopressin in a rat model of trait anxiety.

TL;DR: A role for an AVP gene polymorphism and CBF-A in elevated AVP expression in the PVN of HAB rats likely to contribute to their behavioral and neuroendocrine phenotype is demonstrated.
Journal ArticleDOI

Gonadal influence on agonistic behavior in the male domestic rat

TL;DR: The expression of agonistic behavior was potentiated by androgen; aggressiveness and dominance were also greatly influenced by residence in the home cage.
Journal ArticleDOI

Factor analysis of the DSM-III-R borderline personality disorder criteria in psychiatric inpatients.

TL;DR: Exploratory factor analysis revealed three homogeneous components of borderline personality disorder that may represent personality, behavioral, and affective features central to the disorder and may inform treatment plans.
Journal ArticleDOI

The epidemiology of antisocial personality disorder.

TL;DR: Despite the large amount of research into antisocial personality disorder, longitudinal data are missing and the validity of the diagnosis remains questionable, the paper concludes with recommendations for future research.
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