Preliminary investigation of the influence of dopamine regulating genes on social working memory
Working memory (WM) refers to mental processes that enable temporary retention and manipulation of information, including information about other people ("social working memory"). Previous studies have demonstrated that nonsocial WM is supported by dopamine neurotransmission. Here, we inve...
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Published in | Social neuroscience Vol. 9; no. 5; pp. 437 - 451 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
Colchester
Routledge
01.01.2014
Taylor & Francis Taylor & Francis Ltd |
Subjects | |
Online Access | Get full text |
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Summary: | Working memory (WM) refers to mental processes that enable temporary retention and manipulation of information, including information about other people ("social working memory"). Previous studies have demonstrated that nonsocial WM is supported by dopamine neurotransmission. Here, we investigated in 131 healthy adults whether dopamine is similarly involved in social WM by testing whether social and nonsocial WM are influenced by genetic variants in three genes coding for molecules regulating the availability of dopamine in the brain: catechol-O-methyltransferase (COMT), dopamine active transporter (DAT), and monoamine-oxidase A (MAOA). An advantage for the Met allele of COMT was observed in the two standard WM tasks and in the social WM task. However, the influence of COMT on social WM performance was not accounted for by its influence on either standard WM paradigms. There was no main effect of DAT1 or MAOA, but a significant COMT x DAT1 interaction on social WM performance. This study provides novel preliminary evidence of effects of genetic variants of the dopamine neurotransmitter system on social cognition. The results further suggest that the effects observed on standard WM do not explain the genetic effects on effortful social cognition. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 We wish to thank E. Kilford and N. Bazargani for their help with the testing. The research was funded by a Leverhume grant [F/07134/CZ (P12835)]. SJB is funded by a Royal Society University Research Fellowship. All authors report no biomedical financial interests or potential conflicts of interest. Iroise Dumontheil and Sarah K. G. Jensen contributed equally to this work. |
ISSN: | 1747-0919 1747-0927 |
DOI: | 10.1080/17470919.2014.925503 |