Placebo effects on analgesia related to testosterone and premotor activation

Jae Chan Choi, Do Joon Yi, Bong Soo Han, Phil Hyu Lee, Ji Hyun Kim, Bo Hyun Kim

Research output: Contribution to journalArticle

12 Citations (Scopus)

Abstract

Using functional magnetic resonance imaging, we tested whether graded placebo conditions could modulate the degree of placebo effect and brain activation patterns in study participants and whether the placebo effect could be influenced by hormones. Each participant was investigated under three conditions: the control (no placebo) condition, the low-placebo condition, and the high-placebo condition (HPC). Activations of the premotor areas, anterior cingulate cortex, and prefrontal cortex were stronger in the HPC compared with those in the control and low placebo conditions. The premotor areas were activated by increased testosterone levels under the HPC. These results suggest that testosterone may affect the brain activation and response to pain during a high-placebo response, with the data supported by brain imaging.

Original languageEnglish
Pages (from-to)419-423
Number of pages5
JournalNeuroReport
Volume22
Issue number9
DOIs
Publication statusPublished - 2011 Jun 22

Fingerprint

Placebo Effect
Analgesia
Testosterone
Placebos
Motor Cortex
Gyrus Cinguli
Brain
Prefrontal Cortex
Neuroimaging
Magnetic Resonance Imaging
Hormones
Pain

Keywords

  • Anterior cingulate cortex
  • functional magnetic resonance imaging
  • pain
  • placebo
  • prefrontal cortex
  • premotor
  • testosterone

ASJC Scopus subject areas

  • Neuroscience(all)

Cite this

Placebo effects on analgesia related to testosterone and premotor activation. / Choi, Jae Chan; Yi, Do Joon; Han, Bong Soo; Lee, Phil Hyu; Kim, Ji Hyun; Kim, Bo Hyun.

In: NeuroReport, Vol. 22, No. 9, 22.06.2011, p. 419-423.

Research output: Contribution to journalArticle

Choi, Jae Chan ; Yi, Do Joon ; Han, Bong Soo ; Lee, Phil Hyu ; Kim, Ji Hyun ; Kim, Bo Hyun. / Placebo effects on analgesia related to testosterone and premotor activation. In: NeuroReport. 2011 ; Vol. 22, No. 9. pp. 419-423.
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