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GENERAL ARTICLES

The Effects of Desflurane on the Nervous System: From Spinal Cord to Muscles

Yann Péréon, MD, PhD^*, Jean-Marc Bernard, MD, PhD, Sylvie Nguyen The Tich, MD^*, Robert Genet^*, Florence Petitfaux, , MD, and Pierre Guihéneuc, MD^*

*Départment de Neurophysiologie Clinique, Laboratoire d’Explorations Fonctionnelles, Hôtel-Dieu, Nantes; Départment d’Anesthésie-Réanimation Chirurgicale, Polyclinique Jean-Villar, Bruges-Bordeaux; and Département d’Anesthésie-Réanimation Chirurgicale, Hôtel-Dieu, Nantes, France

Address correspondence and reprint requests to Yann Péréon, MD, PhD, Laboratoire d’Explorations Fonctionnelles, Hôtel-Dieu, F-44093 Nantes Cedex, France. Address e-mail to Yann.Pereon{at}sante.univ-nantes.fr

Monitoring of motor pathways via muscle contraction recording is sensitive to anesthetics, particularly volatile anesthetics. However, the specific action sites of these anesthetics on the spinal cord and the peripheral nervous system are not well known in humans. Therefore, we studied proximal and distal motor and sensory nerve conduction, neuromuscular junction transmission, and spinal cord excitability (H/M amplitude ratio and F-wave amplitude and persistency) using standard neurophysiological techniques in 10 patients who underwent orthopedic surgery. Muscle potentials evoked by spinal cord stimulation were recorded in five additional patients. Desflurane was introduced to achieve end-tidal concentration of 3.7% and 7.4%, in 50% O₂/N₂O and in 100% O₂. Measurements were obtained before desflurane administration and 20 min after obtaining a stable level of each concentration. Peripheral nerve conduction and neuromuscular function were not significantly affected by desflurane. However, spinal cord excitability was significantly decreased by desflurane administration (H/M ratio 37% ± 9%, 12% ± 5%, 7% ± 4% at desflurane concentration 0.0%, 3.7%, and 7.4% in 100% O₂, respectively). Muscle potentials evoked by spinal cord stimulation were abolished by desflurane. These data rule out the possibility that desflurane specifically alters peripheral nerve conduction or synapse transmission at the neuromuscular junction. They demonstrate that desflurane acts preferentially at the level of the spinal motoneuron.

Implications: We used neurophysiological techniques to assess the effects of desflurane on spinal cord conduction and excitability, motor and sensory peripheral nerve conduction, and neuromuscular transmission. Our data demonstrate that desflurane acts preferentially at the level of the spinal motoneuron, providing useful information for neurophysiological monitoring and immobilization during surgery and for minimum alveolar anesthetic concentration definition.

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