A1 Refereed original research article in a scientific journal
Endogenous opioid receptor system mediates costly altruism in the human brain
Authors: Chen Jinglu; Putkinen Vesa; Seppälä Kerttu; Hirvonen Jussi; Ioumpa Kalliopi; Gazzola Valeria; Keysers Christian; Nummenmaa Lauri
Publisher: Springer Nature
Publication year: 2024
Journal: Communications Biology
Journal name in source: Communications Biology
Article number: 1401
Volume: 7
Issue: 1
eISSN: 2399-3642
DOI: https://doi.org/10.1038/s42003-024-07084-7(external)
Web address : http://doi.org/10.1038/s42003-024-07084-7(external)
Self-archived copy’s web address: https://research.utu.fi/converis/portal/detail/Publication/459057556(external)
Functional neuroimaging studies suggest that a large-scale brain network transforms others' pain into its vicarious representation in the observer, potentially modulating helping behavior. However, the neuromolecular basis of individual differences in vicarious pain and helping is poorly understood. We investigated the role of the endogenous μ-opioid receptor (MOR) system in altruistic costly helping. MOR density was measured using [11C]carfentanil. In a separate fMRI experiment, participants could donate money to reduce a confederate's pain from electric shocks. Participants were generally willing to help, and brain activity was observed in amygdala, anterior insula, anterior cingulate cortex (ACC), striatum, primary motor cortex, primary somatosensory cortex and thalamus when witnessing others' pain. Haemodynamic responses were negatively associated with MOR availability in emotion circuits. However, MOR availability positively associated with the ACC and hippocampus during helping. These findings suggest that the endogenous MOR system modulates altruism in the human brain.
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Funding information in the publication:
This work was supported by grants from the Academy of Finland (#332225), Sigrid Juselius Stiftelse, Signe och Ane Gyllenberg’s Stiftelse, and China Scholarship Council (202106040042), as well as grants from the Dutch Research Council (NWO) to V.G. (VIDI grant 452-14-015) and C.K. (VICI grant 453-15-009).