Journal Home
IASP
Search for

Volume 145, Issue 1, Pages 24-30 (September 2009)


View previous. 12 of 46 View next.

Placebo conditioning and placebo analgesia modulate a common brain network during pain anticipation and perception

Alison WatsonaCorresponding Author Informationemail address, Wael El-Deredyb, Gian Domenico Iannettic, Donna Lloydb, Irene Traceyd, Brent A. Vogte, Valerie Nadeaua, Anthony K.P. Jonesa

Received 13 October 2008; received in revised form 23 January 2009; accepted 6 April 2009. published online 12 June 2009.

Refers to article:
Open your mind to placebo conditioning , 26 June 2009
Carlo A. Porro
PAIN®
September 2009 (Vol. 145, Issue 1, Pages 2-3)
Full Text | Full-Text PDF (75 KB)

Abstract 

The neural mechanisms whereby placebo conditioning leads to placebo analgesia remain unclear. In this study we aimed to identify the brain structures activated during placebo conditioning and subsequent placebo analgesia. We induced placebo analgesia by associating a sham treatment with pain reduction and used fMRI to measure brain activity associated with three stages of the placebo response: before, during and after the sham treatment, while participants anticipated and experienced brief laser pain. In the control session participants were explicitly told that the treatment was inactive. The sham treatment group reported a significant reduction in pain rating (p=0.012). Anticipatory brain activity was modulated during placebo conditioning in a fronto-cingulate network involving the left dorsolateral prefrontal cortex (DLPFC), medial frontal cortex and the anterior mid-cingulate cortex (aMCC). Identical areas were modulated during anticipation in the placebo analgesia phase with the addition of the orbitofrontal cortex (OFC). However, during altered pain experience only aMCC, post-central gyrus and posterior cingulate demonstrated altered activity. The common frontal cortical areas modulated during anticipation in both the placebo conditioning and placebo analgesia phases have previously been implicated in placebo analgesia. Our results suggest that the main effect of placebo arises from the reduction of anticipation of pain during placebo conditioning that is subsequently maintained during placebo analgesia.

a Human Pain Research Group, University of Manchester Rheumatic Diseases Centre, Hope Hospital, Salford M6 8HD, UK

b School of Psychological Sciences, University of Manchester, Oxford Rd., Manchester M13 9PL, UK

c Department of Physiology, Anatomy and Genetics, University of Oxford, South Parks Road, OX1 3QX Oxford, UK

d Oxford Centre for Functional MRI of the Brain, Oxford University, Department of Clinical Neurology, John Radcliffe Hospital, Headington, Oxford OX3 9DU, UK

e Department of Neuroscience and Physiology, SUNY Upstate Medical University and Cingulum NeuroSciences Institute, 750E. Adams Street, Syracuse, NY 13210, USA

Corresponding Author InformationCorresponding author. Tel.: +44 161 206 4529.

PII: S0304-3959(09)00209-7

doi:10.1016/j.pain.2009.04.003


View previous. 12 of 46 View next.