Cited by 138Neurotransmitter Receptor Influence on BehaviorPsychopathy, Forensic Psychiatry, Sexual OffendingNeuroendocrine regulation and behavior

The DOI matches its Crossref record; 400 of the 400 references it cites were found in a registry or an index.

The role of monoamine oxidase A in the neurobiology of aggressive, antisocial, and violent behavior: A tale of mice and men

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Kolla, Nathan J., Bortolato, Marco·2020·Progress in Neurobiology

Abstract

Over the past two decades, research has revealed that genetic factors shape the propensity for aggressive, antisocial, and violent behavior. The best-documented gene implicated in aggression is MAOA (Monoamine oxidase A), which encodes the key enzyme for the degradation of serotonin and catecholamines. Congenital MAOA deficiency, as well as low-activity MAOA variants, has been associated with a higher risk for antisocial behavior (ASB) and violence, particularly in males with a history of child maltreatment. Indeed, the interplay between low MAOA genetic variants and early-life adversity is the best-documented gene × environment (G × E) interaction in the pathophysiology of aggression and ASB. Additional evidence indicates that low MAOA activity in the brain is strongly associated with a higher propensity for aggression; furthermore, MAOA inhibition may be one of the primary mechanisms whereby prenatal smoke exposure increases the risk of ASB. Complementary to these lines of evidence, mouse models of Maoa deficiency and G × E interactions exhibit striking similarities with clinical phenotypes, proving to be valuable tools to investigate the neurobiological mechanisms underlying antisocial and aggressive behavior. Here, we provide a comprehensive overview of the current state of the knowledge on the involvement of MAOA in aggression, as defined by preclinical and clinical evidence. In particular, we show how the convergence of human and animal research is proving helpful to our understanding of how MAOA influences antisocial and violent behavior and how it may assist in the development of preventative and therapeutic strategies for aggressive manifestations.

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Research works printed but not linked: 4

  1. Al-Tayie, 2018, Allelic diversity of uVNTR polymorphism in monoamine oxidase A (MAOA) gene in Iraqi population, J. Pharm. Sci. Res., 10, 3099
  2. Bushman, 2010, Aggression, Vol. 2, 833
  3. Moffitt, 2003, Life-course-persistent and adolescent-limited ASB: a 10-year research review and A research agenda, 49
  4. Nemeroff, 2004, Early-life adversity, CRF dysregulation, and vulnerability to mood and anxiety disorders, Psychopharmacol. Bull., 38, 14

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Metadata

Authors
Kolla, N. J., & Bortolato, M.
Affiliations
  • Centre for Addiction and Mental Health (CA)
  • University of Utah (US)
Corresponding author
  • Kolla, Nathan J.
  • Bortolato, Marco
Venue
Progress in Neurobiology
Publisher
Elsevier BV
Published
2020-11
Volume
194
Pages
101875
ISSN
0301-0082 (ISSN-L)
OpenAlex
W3036818139
Cited by
138
References
400
Citations by year
2026: 18 · 2025: 25 · 2024: 29 · 2023: 42 · 2022: 11 · 2021: 12 · 2020: 1
FWCI
2.28
Type
journal article
Language
en
Open access
Locations
  • Progress in Neurobiology (publishedVersion)
  • PubMed (publishedVersion)
  • Europe PMC (PubMed Central) (acceptedVersion)
  • PubMed Central (acceptedVersion)
Funders
National Institutes of Health
Topics
  • Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
  • Social Sciences › Psychology › Clinical Psychology › Psychopathy, Forensic Psychiatry, Sexual Offending
  • Life Sciences › Neuroscience › Endocrine and Autonomic Systems › Neuroendocrine regulation and behavior
Keywords
monoamine oxidase A, aggression, antisocial behavior, violent behavior, gene-environment interaction, child abuse, prenatal tobacco exposure, serotonin, catecholamines, neurobiology of aggression
MeSH terms
Aggression, Animals, Antisocial Personality Disorder, Behavior, Animal, Humans, Monoamine Oxidase, Social Behavior, Violence, Gene-Environment Interaction

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