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Genetics of adult attachment and the endogenous opioid system
Author(s) -
Alfonso Troisi
Publication year - 2022
Publication title -
world journal of psychiatry
Language(s) - English
Resource type - Journals
ISSN - 2220-3206
DOI - 10.5498/wjp.v12.i8.1105
Subject(s) - anterior cingulate cortex , opioid , amygdala , psychology , endogenous opioid , neuroscience , candidate gene , μ opioid receptor , opioid receptor , clinical psychology , medicine , receptor , genetics , biology , gene , cognition
Since the pioneering work by Panksepp et al , the neurobiological bases of attachment behavior have been closely linked with opioid neurotransmission. Candidate gene studies of adult individuals have shown that variation in the mu-opioid receptor gene ( OPRM1 ) influences attachment behavior. Early maternal care and the A/A genotype of the A118G polymorphism interact in modulating levels of fearful attachment. Compared to their counterparts carrying the A/A genotype, individuals expressing the minor 118G allele show lower levels of avoidant attachment and experience more pleasure in social situations. Brain imaging research has strengthened the biological plausibility of candidate gene studies. The avoidance dimension of attachment correlates negatively with mu-opioid receptor availability in the thalamus and anterior cingulate cortex, as well as the frontal cortex, amygdala, and insula. Overall, findings from human studies combined with those from animal models suggest that research on the genetic bases of attachment should include the endogenous opioid system among the investigated variables.

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