Evidence map›Paper›PMID 38328016›Full record

ArticleJournal of pain research2024

Opioid Receptor Mu 1 Gene (OPRM1) A118G Polymorphism and Emotional Modulation of Pain.

Edward A Trimble, Parker A Kell, Matteo A Avella, Christopher R France, Jamie L Rhudy

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Article in Journal of pain research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

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5citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

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5 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Edward A TrimbleDepartment of Biochemistry, The University of Tulsa, Tulsa, OK, USA.
Parker A KellDepartment of Psychology, The University of Tulsa, Tulsa, OK, USA.
Matteo A AvellaDepartment of Biology, The University of Tulsa, Tulsa, OK, USA.
Christopher R FranceDepartment of Psychology, Ohio University, Athens, OH, USA.
Jamie L RhudyDepartment of Psychology, The University of Tulsa, Tulsa, OK, USA.ORCID 0000-0002-5785-1880

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: The A118G polymorphism in the opioid receptor mu 1 gene (OPRM1) is associated with decreased opioid receptor availability, altered emotion, and increased pain. Given that emotions modulate pain (positive emotions inhibit pain, negative emotions enhance pain), we predicted that G allele carriers would experience impaired emotional modulation of pain compared to non-G allele carriers. Patients and Methods: Emotional pictures (ie, erotica, neutral, attack) from the International Affective Picture System were used by permission from the authors to experimentally manipulate emotions in 64 adult participants while painful electrocutaneous stimulations were delivered in a cross-sectional study. Ratings of arousal and valence/pleasure were made in response to pictures, and pain ratings and a physiological measure of spinal nociception (ie, nociceptive flexion reflex, NFR) were collected in response to painful stimulations. Secondary analyses were conducted to examine the relationship between the A118G polymorphism and emotional modulation of pain/NFR. Results: Exposure to emotional pictures elicited similar changes in valence, but G-carriers rated erotic pictures as more arousing. In non-carriers, pain was facilitated by attack pictures and pain and NFR were inhibited by erotic pictures relative to neutral pictures. Among G-carriers, pain was facilitated by negative emotional pictures but there was no pain or NFR inhibition by positive emotional pictures. Conclusion: The altered response to pleasant stimuli further supports the role of opioids in appetitive behavior and describes how the A118G polymorphism may prevent carriers from inhibiting pain during pleasure.

Indexed as

emotiongeneticsopioid receptorpainpain inhibition

Identifiers

PMID38328016
PMCPMC10849056

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