Polymorphism in the µ-opioid receptor gene (OPRM1) modulates neural processing of physical pain, social rejection and error processing

• Published in: Experimental brain research 2015-09, Vol.233 (9), p.2517-2526
• Main Authors: Bonenberger, M., Plener, P. L., Groschwitz, R. C., Grön, G., Abler, B.
• Format: Article
• Language: English
• Subjects: Adolescent; Adult; Biomedical and Life Sciences; Biomedicine; Brain - blood supply; Brain - physiopathology; Brain research; Child & adolescent psychiatry; Decision Making; Electric Stimulation - adverse effects; Feedback; Female; Genotype; Humans; Image Processing, Computer-Assisted; Inhibition (Psychology); Magnetic Resonance Imaging; Medical imaging; Narcotics; Neuroimaging; Neurology; Neurosciences; Oxygen - blood; Pain; Pain - etiology; Pain - genetics; Pain - pathology; Pain Perception - physiology; Polymorphism; Polymorphism, Single Nucleotide - genetics; Psychometrics; Psychotherapy; Receptors, Opioid, mu - genetics; Research Article; Social Distance; User-Computer Interface; Young Adult
• ISSN: 0014-4819; 1432-1106
• DOI: 10.1007/s00221-015-4322-9

Variations of the µ-opioid receptor gene OPRM1 have been shown to modulate pain perception with some evidence pointing towards a modulation of not only physical but also “psychological pain”. In line with suggestions of a common neural network involved in the processing of physical pain and negative and distressing stimuli, like social rejection as a psychologically harmful event, we examined the influence of the A118G polymorphism on the neural processing of physical and non-physical pain. Using fMRI, we investigated a sample of 23 females with the more frequent AA genotype, and eight females with the relatively rare but more pain-sensitive AG genotype during electrical stimulation to the dorsum of the non-dominant hand. Non-physical pain was investigated using Cyberball, a virtual ball-tossing game, to induce experiences of non-self-dependent social rejection. A Go/NoGo task with an increased risk of self-dependent erroneous performance was used as a control task to investigate the effects of negative feedback as a more cognitive form of distress. Relative to A118G homozygous A-allele carriers, G-allele carriers showed significantly increased activation of the supplementary motor area/superior frontal gyrus and the precentral gyrus during electrical stimulation. Increased activation of the secondary sensorimotor cortex (SII) was found during social exclusion and during negative feedback. We demonstrate that brain regions particularly related to the somatosensory component of pain processing are modulated by variations in OPRM1. Influences were evident for both physical and psychological pain processing supporting the assumption of shared neural pathways.