Abstract

The insula, particularly its posterior portion, is often regarded as a primary cortex for pain. However, this interpretation is largely based on reverse inference, and a specific involvement of the insula in pain has never been demonstrated. Taking advantage of the high spatiotemporal resolution of direct intracerebral recordings, we investigated whether the human insula exhibits local field potentials (LFPs) specific for pain. Forty-seven insular sites were investigated. Participants received brief stimuli belonging to four different modalities (nociceptive, vibrotactile, auditory, and visual). Both nociceptive stimuli and non-nociceptive vibrotactile, auditory, and visual stimuli elicited consistent LFPs in the posterior and anterior insula, with matching spatial distributions. Furthermore, a blind source separation procedure showed that nociceptive LFPs are largely explained by multimodal neural activity also contributing to non-nociceptive LFPs. By revealing that LFPs elicited by nociceptive stimuli reflect activity unrelated to nociception and pain, our results confute the widespread assumption that these brain responses are a signature for pain perception and its modulation.

Highlights

  • The human insula, in particular the region encompassing the dorsal posterior insula and the adjacent parietal operculum, is generally believed to play a specific role in the perception of pain

  • A widely accepted notion is that the insula, especially its posterior portion, plays a specific role in the perception of pain

  • We demonstrate that painful and nonpainful stimuli elicit very similar responses throughout the human insula

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Summary

Introduction

The human insula, in particular the region encompassing the dorsal posterior insula and the adjacent parietal operculum, is generally believed to play a specific role in the perception of pain. Depth recordings in humans have shown that nociceptive stimuli elicit robust LFPs in this region, considered to reflect early stages of cortical processing related to the perception of pain [6,7,8,9]. Segerdahl et al [18] recently demonstrated a significant correlation between long-lasting changes in absolute cerebral blood flow (CBF) in the dorsal posterior insula and the intensity of perceived ongoing pain. All these observations provide support for a specific involvement of the insula in pain perception

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