По всем вопросам звоните:

+7 495 274-22-22

УДК: 61:159.923 DOI:10.33920/med-01-2112-07

Психофизиология и психофармакология агрессии

Астаулов Никита Дмитриевич студент, кафедра психиатрии и медицинской психологии, ГАФОУ ВО РУДН, г. Москва, nikitaastaulov@gmail.com, orcid 0000-0002-6204-141X
Артемьева Марина Станиславовна профессор, д.м.н, профессор кафедры психиатрии и медицинской психологии, ГАФОУ ВО РУДН, г. Москва, e- mail msartemieva@mail.ru, ORCID: 0000-00028713-1438
Шумейко Денис Евгеньевич врач психиатр, ПСО номер 2, ГКБ имени Емирашанцева ДЗМ, аспирант кафедры психиатрии и медицинской психологии, ГАФОУ ВО РУДН, г. Москва, dsadovoi@gmail.com, orcid 0000-0002-5449-8444

Статья посвящена психофизиологическим механизмам формирования агрессивного поведения и возможным путям его медикаментозной коррекции. По данным литературы выявлены три основные патофизиологических синдрома при агрессии: гиперперфузия темпоральной и фронтальной долей мозга, дисфункция серотониновой системы и метаболизма глюкозы в темпоральной коре.

Литература:

1. Kolla NJ Houle S. Single-Photon Emission Computed Tomography and Positron Emission Tomography Studies of Antisocial Personality Disorder and Aggression: a Targeted Review. Toronto: Current Psychiatry Reports; 2019.

2. Robins LN, Regier DA. Psychiatric disorders in America. New York: Free Press; 1991.

3. Samuels J, Bienvenu OJ, Cullen B, Costa PT Jr, Eaton WW, Nestadt G. Personality dimensions and criminal arrest. Compr Psychiatry. 2004; 45 (4): 275–80.

4. Kuruoglu AC, Arikan Z, Vural G, Karatas M, Arac M, Isik E. Single photon emission computerised tomography in chronic alcoholism. Antisocial personality disorder may be associated with decreased frontal perfusion. Br J Psychiatry. 1996; 169 (3): 348–54.

5. Gerra G, Calbiani B, Zaimovic A, Sartori R, Ugolotti G, Ippolito L, et al. Regional cerebral blood flow and comorbid diagnosis in abstinent opioid addicts. Psychiatry Res. 1998; 83 (2): 117–26.

6. Soderstrom H, Hultin L, Tullberg M, Wikkelso C, Ekholm S, Forsman A. Reduced frontotemporal perfusion in psychopathic personality. Psychiatry Res. 2002; 114 (2): 81–94.

7. Meyer JH, Wilson AA, Rusjan P, Clark M, Houle S, Woodside S, et al. Serotonin2A receptor binding potential in people with aggressive and violent behavior. J Psychiatry Neurosci. 2008; 33 (6): 499–508.

8. Rosell DR, Thompson JL, Slifstein M, Xu X, Frankle WG, New AS, et al. Increased serotonin 2A receptor availability in the orbitofrontal cortex of physically aggressive personality disordered patients. Biol Psychiatry. 2010; 67 (12): 1154–62.

9. New AS, Hazlett EA, Buchsbaum MS, Goodman M, Reynolds D, Mitropoulou V, et al. Blunted prefrontal cortical 18fluorodeoxyglucose positron emission tomography response to meta-chlorophenylpiperazine in impulsive aggression. Arch Gen Psychiatry. 2002; 59 (7): 621–9.

10. Baumann MH, Mash DC, Staley JK. The serotonin agonist m-chlorophenylpiperazine (mCPP) binds to serotonin transporter sites in human brain. Neuroreport. 1995; 6 (16): 2150–2.

11. Seidenwurm D, Pounds TR, Globus A, Valk PE. Abnormal temporal lobe metabolism in violent subjects: correlation of imaging and neuropsychiatric findings. Am J Neuroradiol. 1997; 18 (4): 625–31.

12. Volkow ND, Tancredi LR, Grant C, Gillespie H, Valentine A, Mullani N, et al. Brain glucose metabolism in violent psychiatric patients: a preliminary study. Psychiatry Res. 1995; 61 (4): 243–53.

13. Scott JP Theoretical issues concerning the origin and causes of fighting // The physiology of aggression and defeat. — Springer, Boston, MA, 1971. — S. 11–41.

14. Eleftheriou BE et al. (ed.). Physiology of Aggression and Defeat. — New York: Plenum Press, 1971. — S. 65–90.

15. Scott JP Agonistic behavior of mice and rats: A review // American zoologist. — 1966. — T. 6. — No. 4. — S. 683–701.

16. Kudryavtseva NN Kudryavtseva NN Practice of research of agonistic behavior: Methods, methodology, interpretation. — 2012.

17. Kudryavtseva NN et al. Changes in the activity of tryptophan hydroxylase in the brain during the formation of an aggressive type of behavior in male mice // Reports of the Academy of Sciences. — Federal State Unitary Enterprise Academic Research and Publishing, Production, Printing and Book Distribution Center Nauka, 1997. — T. 357. — №. 3. — S. 424–426.

18. Kudryavtseva NN, Bakshtanovskaya IV Influence of the experience of aggression and submission on the state of mediator systems in different parts of the brain in mice / NN Kudryavtseva, IV Bakshtanovskaya // Preprint. Novosibirsk. — 1989.

19. Ginsberg SD et al. Differential regulation of catechol-O-methyltransferase expression in a mouse model of aggression // Brain Structure and Function. — 2011. — T. 216. — No. 4. — P. 347.

20. Bondar NP, Smagin DA, Kudryavtseva NN Effects of single and chronic administration of naltrexone on agonistic behavior of male mice with repeated experience of aggression // Psychopharmacology and biological narcology. — 2011. — T. 11. — No. 1–2.

21. Kudryavtseva NN et al. Modulation of anxiety-related behaviors by μ-and κ-opioid receptor agonists depends on the social status of mice // Peptides. — 2004. — T. 25. — No. 8. — S. 1355–1363.

22. Rodgers RJ The elevated plus-maze: pharmacology, methodology and ethology // Ethology and psychopharmacology. — 1994. — S. 9–44.

23. Lipina TV et al. Differences in the effects of naltrexone on communicative and aggressive behavior in individuals with different experiences of social victories // Experimental wedge pharmacol. — 1998. — T. 61. — No. 3. — S. 13–18.

24. Bondar NP, Kudryavtseva NN The effect of buspirone on the aggressive and anxious behavior of male mice with different experiences of aggression // Experimental and Clinical Pharmacology. — 2003. — T. 66. — No. 4. — S. 12–16.

25. Kudryavtseva NN, Bondar NP Anxiolytic and anxiogenic effects of diazepam in male mice with different experiences of aggression // Bull Experimental Biol Med. — 2002. — T. 133. — No. 4. — S. 429–433.

26. Smagin DA, Bondar NP, Kudryavtseva NN Effect of sodium valproate on the aggressive behavior of male mice with different experiences of aggression // Experimental and Clinical Pharmacology. — 2010. — T. 73. — No. 1. — S. 10–15.

27. Sheard MH et al. The effect of lithium on impulsive aggressive behavior in man // The American journal of psychiatry. — 1976.

28. Kudryavtseva, Natalia Nikolaevna. The neurobiology of aggression: mice and people: N.N. Kudryavtseva. — Novosibirsk: Nauka-Center, 2013. — 271 p.: ill., table; 22 cm; ISBN 978-5-9554-0028-4

Aggression is one of the most dangerous and frightening phenomena. We hear about murder, domestic violence, war and crime every day. Of course, there are many modern social and political ways to control the level of aggression of both a person and society with the help of organizations such as the UN, peacekeeping missions, charitable organizations and foundations, as well as modern medicine and psychotherapy that can help both individuals and groups. Despite this and the fact that there are now no global armed conflicts, the issue of violence and terrible forms in which it manifests is still an acute problem. In this work, we write about an alternative direction that can help cope — the psychopharmacology of aggression. This area is currently poorly developed, but we hope that over time the situation will change. Here is an analysis of the literature on this topic.

As a result of a meta-analysis of the literature, phenomena were found in which pathological aggression occurs. From a medical point of view, according to research [1], the most reliable material for the study of aggression is people with antisocial disorder (APD-F60.2) [2].

A characteristic feature of APS is a decrease in overall cerebral blood flow, while hypoperfusion of the anterior frontal and temporal lobes. There was a significant negative correlation between the severity of APD and frontal and temporal increased perfusion. Since the frontal lobes are involved in the regulation of aggression, structural changes in them can lead to impulsive aggression [3,4,5,6]. Since it is believed that the frontal cortex is responsible for personality, will, and morality, it can be assumed that its insufficient blood circulation can weaken personal and moral control over aggression, which requires further study.

We examined studies using labeled serotonin ligand in a sample of patients with APD and a history of violent behavior. They showed a decrease in the density of serotonin receptors in the dorsolateral prefrontal cortex in people with ARL aged 19–24 years compared with controls. While at the age of 25–33 no changes were found. Another study showed that at the age of 34–39 years, on the contrary, there is an increase in the activity of serotonin receptors in the prefrontal cortex. The authors of the study found a correlation between a decrease in the activity of serotonin receptors at the age of 19–24 and data that at this age people more often commit aggressive acts, including criminally actions [7] for further study. Also, studies of people with APD using serotonin labeled ligands showed their deactivation in the left anteromedial orbital cortex and in the left anterior cingulate gyrus, which is usually activated in healthy people by the administration of metachlorophenylpiperazine. On the other hand, the posterior tortuous gyrus was activated in impulsive patients and deactivated in healthy ones. No group differences were found on the baseline scan. The authors interpret their results as follows: activation of the anterior cingulate gyrus and posterior orbital cortex, together with serotonergic effects, can inhibit aggressive behavior.

Для Цитирования:
Астаулов Никита Дмитриевич, Артемьева Марина Станиславовна, Шумейко Денис Евгеньевич, Психофизиология и психофармакология агрессии. Вестник неврологии, психиатрии и нейрохирургии. 2021;12.
Полная версия статьи доступна подписчикам журнала
Язык статьи:
Действия с выбранными: