Abstract

The dorsolateral prefrontal cortex (dlPFC) is functionally linked to the descending pain modulation system and has been implicated in top down pain inhibition, including placebo analgesia. Therefore, functions of the dlPFC may be impaired in patients with chronic pain. Postherpetic neuralgia (PHN) is one of several syndromes with chronic neuropathic pain. In the present study, we investigated possible dysfunction of the dlPFC in chronic pain using patients with PHN. In a conditioning phase, heathy controls (n = 15) and patients with PHN (n = 7) were exposed to low (LF) and high (HF) frequency tones associated with noxious stimuli: weak (WS) and strong (SS) electrical stimulation, respectively. After the conditioning, cerebral hemodynamic activity was recorded from the bilateral dlPFC while the subjects were subjected to the cue tone-noxious electrical stimulation paradigm, in which incorrectly cued noxious stimuli were sometimes delivered to induce placebo and nocebo effects. The results indicated that hemodynamic responses to the LF tone in the right dlPFC was significantly lower in patients with PHN compared to the healthy controls. Furthermore, the same hemodynamic responses in the right dlPFC were correlated with placebo effects. In addition, clinical symptoms of PHN were negatively correlated to cerebral hemodynamic responses in the right dlPFC and magnitudes of the placebo effects. The results suggest that the right dlPFC, which is closely associated with the descending pain modulation system, is disturbed in PHN.

Highlights

  • One-third to one-half of the population suffers from chronic pain (Fayaz et al, 2016)

  • Previous studies reported a dorsolateral prefrontal cortex (dlPFC) involvement in placebo effects in response to CSs associated with safe stimuli through its effects on the descending pain modulation system in heathy subjects

  • These findings suggest that the dlPFC might be disturbed in patients with chronic pain

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Summary

Introduction

One-third to one-half of the population suffers from chronic pain (Fayaz et al, 2016). Postherpetic neuralgia (PHN) is a typical chronic neuropathic pain syndrome consisting of symptoms such as spontaneous pain, tactile allodynia, and hyperpathia, which may develop after the healing of herpes zoster eruptions. Several studies suggest that disturbance of the descending pain modulation system is involved in the development of chronic pain (see review by Ossipov et al, 2014). A recent clinical study reported that conditioned pain modulation was disturbed in patients with PHN, and impairment in conditioned pain modulation was correlated with clinical pain symptoms (Pickering et al, 2014). These findings suggest that the pain-inhibition system is disturbed in PHN (Pickering et al, 2014)

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