Clinical section
Neural generators of N18 and P14 far-field somatosensory evoked potentials studied in patients with lesion of thalamus or thalamo-cortical radiationsGénérateurs des composantes far field P14 et N18 des potentiels évoqués somesthésiques: malades avec lésion du thalamus ou des radiations thalamo-corticales

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Abstract

Somatosensory evoked potentials (SEPs) to electrical stimulation of the right or left median nerve were studied in 4 patients with hemianesthesia and a severe thalamic or suprathalamic vascular lesion on one side. The SEPs were recorded with a non-cephalic reference. The normal side of each patient served as his or her own control. The lesion consistently abolished the parietal N20-P27-P45 and the prerolandic P22-N30 SEP components. It did not significantly affect the P9-P11-P14 positive far fields, nor the widespread bilateral N18 SEP component. This allowed N18 features to be studied without interference from cortical components. It is proposed that N18 reflects several deeply located generators in brain stem and/or thalamus whereas N20 represents the earliest cortical response of the contralateral post- central receiving areas.

Résumé

Les potentiels évoqués somesthésiques (PES) à la stimulation électrique du nerf médian gauche ou droit ont été étudiés chez 4 malades avec une lésion vasculaire grave thalamique ou suprathalamique unilatérale et une hémianesthésie clinique. Les PES ont été enregistrés avec référence non-céphalique. Le côté normal a servi de contrôle. La lésion a chaque fois aboli les composantes pariétales N20-P27-P45 et prérolandiques P22-N30. Elle n'a pas modifié significativement les far fields P9-P11-P14, ni la composante diffuse bilatérale N18. Il a donc été possible d'étudier le N18 sans interférence des composantes corticales. Le N18 est produit par plusieurs générateurs profonds situés dans le tronc cérébral et/ou le thalamus, alors que le N20 représente la réponse corticale précoce des aires postcentrales de projection somesthésique.

References (39)

  • D.R. Humphrey

    Re-analysis of the antidromic cortical response. On the contribution of cell discharge and PSPs to the evoked potentials

    Electroenceph. clin. Neurophysiol.

    (1968)
  • T. Nakanishi et al.

    The initial positive component of scalp-recorded somatosensory evoked potentials in normal subjects and in patients with neurological disorders

    Electroenceph. clin. Neurophysiol.

    (1978)
  • J. Siivola et al.

    Somatosensory evoked potentials in cervical spondylosis and herniated disc

    Electroenceph. clin. Neurophysiol.

    (1981)
  • C. Baleydier et al.

    Projections of the ascending somesthetic pathways to the cat superior colliculus visualized by the HRP technique

    Exp. Brain Res.

    (1978)
  • D. Bowsher

    The termination of secondary somatosensory neurons within the thalamus of Macaca mulatta: an experimental degeneration study

    J. comp. Neurol.

    (1961)
  • K.H. Chiappa et al.

    Evoked potentials in clinical medicine

    New Engl. J. Med.

    (1982)
  • K.H. Chiappa et al.

    Short-latency somatosensory evoked potentials following median nerve stimulation in patients with neurological lesions

  • E.J. Colon et al.

    Somatosensory evoked responses in controlled A-alpha sensory fiber disease

    J. Neurol.

    (1978)
  • J.E. Desmedt

    Somatosensory cerebral evoked potentials in man

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    This research has been supported by grants from the Fonds de la Recherche Scientifique Médicale, Belgium

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