The network interaction of the neurocytocine system in the context of social adaptation of children with autism spectrum disorders

 
PIIS102872210002386-9-1
DOI10.31857/S102872210002386-9
Publication type Article
Status Published
Authors
Affiliation: Chelyabinsk State University
Affiliation: Chelyabinsk State University
Affiliation: Chelyabinsk State University
Journal nameRossiiskii immunologicheskii zhurnal
EditionVolume 12 Issue 3
Pages227-232
Abstract

The paper presents the results of the study of neurocytokine interactions in children with autism spectrum disorders with diff erent levels of social adaptation. Two excellent images of functional networks were revealed: in the group “ASD, social contact” – a network with a small number of correlation links – “image of delayed neurodevelopment”; in the group “ASD, without social contact” – the network of correlations is tense, indicating the activation of the sympathetic-adrenal axis, which is the base in the adaptation reaction “fi ght/ fl ight” or “frozen behavior” – the image of the “closed system”. 

Keywordscytokines, neurohormones, children, autism spectrum disorders
Received22.11.2018
Publication date12.01.2019
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1. Di Cicco-Bloom E., Lord C., Zwaigenbaum L., Cour chesne E., Dager S. R., Schmitz C., Schultz R. T., Crawley J., Young L. J. The developmental neurobiology of autism spectrum disorder. J. Neurosci., 2006, 26(26), 6897–6096

2. Baron-Cohen S. Editorial Perspective: Neurodiversity – a revolutionary concept for autism and psychiatry. J. Child. Psychol. Psychiatry, 2017, 58(6), 744–747

3. Skuse D. H., Gallagher L. Dopaminergic-neuropeptide interactions in the social brain. Trends Cogn. Sci., 2008, 13(1), 27–35.

4. Porges S. W. The polyvagal perspective. Bio. Psychol., 2007, 74(2), 116–143

5. Klein J. T., Shepherd S. V., Platt M. L. Social attention and the brain. Curr. Biol., 2009, 19(20), 958–962

6. Rizzolatti G., Craighero L. The mirror-neuron system. Annu. Rev. Neurosci., 2004, 27, 169–192.

7. Adolphs R. Is the human amygdala specialized for processing social information? Ann. N. Y. Acad. Sci., 2003, 985, 326–340.

8. Kirsch P., Esslinger C., Chen Q., Mier D., LisvS., Siddhanti S., Gruppe H., Mattay V. S., Gallhofer B., Meyer- Lindenberg A. Oxytocin modulates neural circuitry for social cognition and fear in humans. J. Neurosci., 2005, 25 (49, 11489–11493.)

9. Guastella A. J., Mitchell P. B., Dadds M. R. Oxytocin increases gaze to the eye region of human faces. Biol. Psychiatry, 2008, 63 (1), 3–5.

10. Campbell A. Attachment, aggression and affi liation: the role of oxytocin in female social behavior.Biol. Psychol., 2008, 77 (1), 1–10

11. Naglova H., Bucova M. HMGB1 and its physiological and pathological roles. Bratisl. Lek. Listy., 2012, 113(3), 163–171.

12. Goldstein D. S., Eisenhofer G., Kopin I. J. Sources and signifi cance of plasma levels of catechols and ther metabolites in humans. J. Pharmacol. Exp. Ther., 2003, 305 (3), 800–811.

13. Baskerville T. A., Douglas A. J. Dopamine and oxytocin interactions underlying behaviors: potential contributions to behavioral disorders. CNS Neurosci. Ther., 2010, 16(3), 92–123.

14. Cunningham E. T. Jr., De Souza E. B. Interleukin 1 receptor in the brain and endocrine tissue. Immunol. Today, 1993, 14(4), 171–176.

15. Goshen I., Yirmiva R. Interleukin-1 (IL-1): a central regulator of stress responses. Front. Neuroendocrinol., 2009, 30(1), 30–45.

16. Ferguson B. J., Marler S., Altstein L. L. et al. Associations between cytokines, endocrine stress response, and gastrointestinal symptoms in autism spectrum disorder. Brain Behav. Immun., 2016, 58, 57–62.

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