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. 2025 Nov 7:38:105591.
doi: 10.1016/j.jpain.2025.105591. Online ahead of print.

Cortico-midbrain-spinal mechanisms underlying placebo analgesia

Affiliations

Cortico-midbrain-spinal mechanisms underlying placebo analgesia

Jeff Boissoneault et al. J Pain. .

Abstract

Past research has demonstrated that pain experience can be manipulated through non-specific effects. Placebo analgesia (PA) is known to be sensitive to an individual's expectations of pain relief. This study aimed to investigate the relationship between the spinal cord, midbrain, and cortical regions commonly associated with expectancy-induced PA. Fifty healthy participants underwent separate brain and spinal fMRI scans involving application of painful heat in four conditions: baseline, placebo analgesia (PA), placebo match (PM; i.e., stimulus adjusted to match PA pain intensity), and repeated baseline (RB). PA was induced through a verbal expectation manipulation with an inert cream. Pain-related functional connectivity (FC) between the dorsolateral prefrontal cortex and periaqueductal gray (PAG), as well as right dorsal C6 and PAG, was calculated. Pain-related functional activation in right dorsal C6 and PAG was also characterized. Results demonstrated a significant placebo analgesic response with decreased pain intensity from baseline to PA conditions. Spinal cord FC revealed greater activation in the periaqueductal gray (PAG) and right dorsal C6 during PA compared to baseline. PAG-C6 FC was significant in all conditions except baseline and was positively associated with pain intensity and expected pain in the PA condition. Double mediation analysis indicated an indirect effect of expected pain on pain intensity through PAG-C6 FC in the PA condition. These findings highlight the critical role of the midbrain-spinal cord pathway in translating expectancy-based placebo into a reduction of perceived pain intensity and underscore the importance of considering cortico-midbrain-spinal mechanisms in understanding placebo analgesia. PERSPECTIVE: Prior neuroimaging studies suggest placebo-related pain reduction is an active pain modulatory process. However, these studies typically do not integrate both spinal and brain fMRI within the same cohort. Combining modalities, our results suggest an important role for midbrain-spinal connectivity as a mediator of expectancy-based placebo analgesia.

Keywords: Expectancy; FMRI; Pain; Placebo; Spinal cord.

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Conflict of interest statement

Disclosures

The authors declare no conflict of interest. This work was supported by the National Center of Complementary and Integrative Health (R01AT001424; M. Robinson, PI). A portion of this work was performed in the McKnight Brain Institute at the National High Magnetic Field Laboratory’s AMRIS Facility, which is supported by National Science Foundation Cooperative Agreement No. DMR-1157490, and the State of Florida.

References

    1. Price DD, Fillingim RB, Robinson ME. Placebo analgesia: friend or foe? Curr Rheumatol Rep. 2006;8(6):418–424. - PubMed
    1. Chung SK, Price DD, Verne GN, Robinson ME. Revelation of a personal placebo response: its effects on mood, attitudes and future placebo responding. Pain. 2007;132(3):281–288. doi: 10.1016/j.pain.2007.01.034 - DOI - PMC - PubMed
    1. Geers AL, Wellman JA, Fowler SL, Helfer SG, France CR. Dispositional optimism predicts placebo analgesia. J Pain. 2010;11(11):1165–1171. doi: 10.1016/j.jpain.2010.02.014 - DOI - PMC - PubMed
    1. Pecina M, Stohler CS, Zubieta JK. Neurobiology of placebo effects: expectations or learning? Soc Cogn Affect Neurosci. 2014;9(7):1013–1021. doi: 10.1093/scan/nst079 - DOI - PMC - PubMed
    1. Pitman RK, van der Kolk BA, Orr SP, Greenberg MS. Naloxone-reversible analgesic response to combat-related stimuli in posttraumatic stress disorder. A pilot study. Arch Gen Psychiatry. 1990;47(6):541–544. - PubMed

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