Literature DB >> 25632140

Local morphology predicts functional organization of experienced value signals in the human orbitofrontal cortex.

Yansong Li1, Guillaume Sescousse2, Céline Amiez3, Jean-Claude Dreher1.   

Abstract

Experienced value representations within the human orbitofrontal cortex (OFC) are thought to be organized through an antero-posterior gradient corresponding to secondary versus primary rewards. Whether this gradient depends upon specific morphological features within this region, which displays considerable intersubject variability, remains unknown. To test the existence of such relationships, we performed a subject-by-subject analysis of fMRI data taking into account the local morphology of each individual. We tested 38 subjects engaged in a simple incentive delay task manipulating both monetary and visual erotic rewards, focusing on reward outcome (experienced value signal). The results showed reliable and dissociable primary (erotic) and secondary (monetary) experienced value signals at specific OFC sulci locations. More specifically, experienced value signal induced by monetary reward outcome was systematically located in the rostral portion of the medial orbital sulcus. Experienced value signal related to erotic reward outcome was located more posteriorly, that is, at the intersection between the caudal portion of the medial orbital sulcus and transverse orbital sulcus. Thus, the localizations of distinct experienced value signals can be predicted from the organization of the human orbitofrontal sulci. This study provides insights into the anatomo-functional parcellation of the anteroposterior OFC gradient observed for secondary versus primary rewards because there is a direct relationship between value signals at the time of reward outcome and unique OFC sulci locations.
Copyright © 2015 the authors 0270-6474/15/351648-11$15.00/0.

Entities:  

Keywords:  experienced value; fMRI; local morphology; orbitofrontal cortex; reward

Mesh:

Substances:

Year:  2015        PMID: 25632140      PMCID: PMC6795255          DOI: 10.1523/JNEUROSCI.3058-14.2015

Source DB:  PubMed          Journal:  J Neurosci        ISSN: 0270-6474            Impact factor:   6.167


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