TY - JOUR
T1 - Brain activity associated with expectancy-enhanced placebo analgesia as measured by functional magnetic resonance imaging
AU - Kong, Jian
AU - Gollub, Randy L.
AU - Rosman, Ilana S.
AU - Megan Webb, J.
AU - Vangel, Mark G.
AU - Kirsch, Irving
AU - Kaptchuk, Ted J.
PY - 2006/1/11
Y1 - 2006/1/11
N2 - In this study, a well established expectancy manipulation model was combined with a novel placebo intervention, a validated sham acupuncture needle, to investigate the brain network involved in placebo analgesia. Sixteen subjects completed the experiment. We found that after placebo acupuncture treatment, subjective pain rating reduction (pre minus post) on the placebo-treated side was significantly greater than on the control side. When we calculated the contrast that subtracts the functional magnetic resonance imaging (fMRI) signal difference between post-treatment and pretreatment during pain application on placebo side from the same difference on control side [e.g., placebo (post - pre) - control (post - pre)], significant differences were observed in the bilateral rostral anterior cingulate cortex (rACC), lateral prefrontal cortex, right anterior insula, supramarginal gyrus, and left inferior parietal lobule. The simple regression (correlation) analysis between each subject's fMRI signal difference of post-treatment and pretreatment difference on placebo and control side and the corresponding subjective pain rating difference showed that significant negative correlation was observed in the bilateral lateral/orbital prefrontal cortex, rACC, cerebellum, right fusiform, parahippocampus, and pons. These results are different from a previous study that found decreased activity in pain-sensitive regions such as the thalamus, insula, and ACC when comparing the response to noxious stimuli applied to control and placebo cream-treated areas of the skin. Our results suggest that placebo analgesiamay be configured through multiple brain pathways and mechanisms.
AB - In this study, a well established expectancy manipulation model was combined with a novel placebo intervention, a validated sham acupuncture needle, to investigate the brain network involved in placebo analgesia. Sixteen subjects completed the experiment. We found that after placebo acupuncture treatment, subjective pain rating reduction (pre minus post) on the placebo-treated side was significantly greater than on the control side. When we calculated the contrast that subtracts the functional magnetic resonance imaging (fMRI) signal difference between post-treatment and pretreatment during pain application on placebo side from the same difference on control side [e.g., placebo (post - pre) - control (post - pre)], significant differences were observed in the bilateral rostral anterior cingulate cortex (rACC), lateral prefrontal cortex, right anterior insula, supramarginal gyrus, and left inferior parietal lobule. The simple regression (correlation) analysis between each subject's fMRI signal difference of post-treatment and pretreatment difference on placebo and control side and the corresponding subjective pain rating difference showed that significant negative correlation was observed in the bilateral lateral/orbital prefrontal cortex, rACC, cerebellum, right fusiform, parahippocampus, and pons. These results are different from a previous study that found decreased activity in pain-sensitive regions such as the thalamus, insula, and ACC when comparing the response to noxious stimuli applied to control and placebo cream-treated areas of the skin. Our results suggest that placebo analgesiamay be configured through multiple brain pathways and mechanisms.
KW - Expectancy
KW - Expectancy manipulation
KW - Pain
KW - Placebo
KW - Placebo acupuncture needle
KW - Placebo analgesia
KW - Steitberger needle
UR - https://www.scopus.com/pages/publications/32544444712
U2 - 10.1523/JNEUROSCI.3556-05.2006
DO - 10.1523/JNEUROSCI.3556-05.2006
M3 - Article
C2 - 16407533
AN - SCOPUS:32544444712
SN - 0270-6474
VL - 26
SP - 381
EP - 388
JO - Journal of Neuroscience
JF - Journal of Neuroscience
IS - 2
ER -