PAIN
Volume 137, Issue 3 , Pages 589-599, 31 July 2008

Laser evoked responses to painful stimulation persist during sleep and predict subsequent arousals

  • H. Bastuji

      Affiliations

    • INSERM, U 879 (Central Integration of Pain), Bron F-69677, France
    • Université Claude Bernard, Lyon F-69003, France
    • Hospices Civils de Lyon, Unité d’Hypnologie, Hôpital Neurologique, 59, Bd Pinel, Bron F-69677, France
    • Corresponding Author InformationCorresponding author. Address: Hospices Civils de Lyon, Unité d’Hypnologie, Hôpital Neurologique, 59, Bd Pinel, Bron F-69677, France. Tel.: +33 4 72 35 78 28; fax: +33 4 72 35 73 97.
  • ,
  • C. Perchet

      Affiliations

    • INSERM, U 879 (Central Integration of Pain), Bron F-69677, France
    • Université Claude Bernard, Lyon F-69003, France
  • ,
  • V. Legrain

      Affiliations

    • Université catholique de Louvain, Unité de Neurosciences Cognitives, Faculté de Psychologie et des Sciences de l’Education, Louvain-la-Neuve B-1348, Belgium
  • ,
  • C. Montes

      Affiliations

    • Universidad de Malaga, Facultad de Medicina, Dept de Physiologia, Malaga E-29080, Spain
  • ,
  • L. Garcia-Larrea

      Affiliations

    • INSERM, U 879 (Central Integration of Pain), Bron F-69677, France
    • Université Claude Bernard, Lyon F-69003, France

Received 2 May 2007; received in revised form 2 October 2007; accepted 22 October 2007. published online 03 December 2007.

Abstract 

We studied behavioural responses and 32-channel brain potentials to nociceptive stimuli during all-night sleep in 12 healthy subjects, using sequences of thermal laser pulses delivered over the dorsum of the hand. Laser stimuli less than 20dB over perception threshold had clear awakening properties, in accordance with the intrinsic threatening value of nociceptive signals. Even in cases where nociceptive stimulation did not interrupt sleep, it triggered motor responses in 11% of trials. Only four subjects reported dreams, and on morning questionnaires there was no evidence of incorporation to dreams of nociceptive stimuli. Contrary to previous reports suggesting the absence of cortical nociceptive responses during sleep, we were able to record brain-evoked potentials to laser (LEPs) during all sleep stages. Sleep LEPs were in general attenuated, but their morphology was sleep-stage-dependent: in stage 2, the weakened initial response was often followed by a high-amplitude negative wave with typical features of a K-complex. During paradoxical sleep (PS) LEP morphology was similar to that of waking, but frontal components showed strong attenuation, consistent with the reported frontal metabolic deactivation. A late positive component (450–650ms) was recorded in both stage 2 and PS, the amplitude of which was significantly enhanced in trials that were followed by an arousal. This response appeared functionally related to the P3 wave, which in waking subjects has been associated to conscious perception and memory encoding.

Keywords: Pain, Sleep, Laser evoked potential, LEP, Cognition

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PII: S0304-3959(07)00637-9

doi:10.1016/j.pain.2007.10.027

PAIN
Volume 137, Issue 3 , Pages 589-599, 31 July 2008