Propofol reduces the amplitude of transcranial electrical motor-evoked potential without affecting spinal motor neurons: a prospective, single-arm, interventional study.

Evoked electromyogram General anesthesia Intraoperative monitoring Motor-evoked potential Propofol

Journal

Journal of anesthesia
ISSN: 1438-8359
Titre abrégé: J Anesth
Pays: Japan
ID NLM: 8905667

Informations de publication

Date de publication:
06 2021
Historique:
received: 20 12 2020
accepted: 22 03 2021
pubmed: 8 4 2021
medline: 9 7 2021
entrez: 7 4 2021
Statut: ppublish

Résumé

Propofol inhibits the amplitudes of transcranial electrical motor-evoked potentials (TCE-MEP) in a dose-dependent manner. However, the mechanisms of this effect remain unknown. Hence, we investigated the spinal mechanisms of the inhibitory effect of propofol on TCE-MEP amplitudes by evaluating evoked electromyograms (H-reflex and F-wave) under general anesthesia. We conducted a prospective, single-arm, interventional study including 15 patients scheduled for spine surgery under general anesthesia. Evoked electromyograms of the soleus muscle and TCE-MEPs were measured at three propofol concentrations using target-controlled infusion (TCI: 2.0, 3.0, and 4.0 µg/mL). The primary outcome measure was the left H-reflex amplitude during TCI of 4.0- compared to 2.0-µg/mL propofol administration. The median [interquartile range] amplitudes of the left H-reflex were 4.71 [3.42-6.60] and 5.6 [4.17-7.46] in the 4.0- and 2.0-μg/mL TCI groups (p = 0.4, Friedman test), respectively. There were no significant differences in the amplitudes of the right H-reflex and the bilateral F-wave among these groups. However, the TCE-MEP amplitudes significantly decreased with increased propofol concentrations (p < 0.001, Friedman test). Propofol did not affect the amplitudes of the H-reflex and the F-wave, whereas TCE-MEP amplitudes were reduced at higher propofol concentrations. These results suggested that propofol can suppress the TCE-MEP amplitude by inhibiting the supraspinal motor pathways more strongly than the excitability of the motor neurons in the spinal cord.

Identifiants

pubmed: 33825982
doi: 10.1007/s00540-021-02927-7
pii: 10.1007/s00540-021-02927-7
doi:

Substances chimiques

Propofol YI7VU623SF

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

434-441

Subventions

Organisme : Japan Society for the Promotion of Science
ID : 18K16441

Références

Pelosi L, Lamb J, Grevitt M, Mehdian S, Webb J, Blumhardt L. Combined monitoring of motor and somatosensory evoked potentials in orthopaedic spinal surgery. Clin Neurophysiol. 2002;113:1082–91.
doi: 10.1016/S1388-2457(02)00027-5
Langeloo DD, Lelivelt A, Journée HL, Slappendel R, de Kleuver M. Transcranial electrical motor-evoked potential monitoring during surgery for spinal deformity: a study of 145 patients. Spine (Phila Pa 1976). 2003;28:1043–50.
Gonzalez AA, Jeyanandarajan D, Hansen C, Zada G, Hsieh PC. Intraoperative neurophysiological monitoring during spine surgery: a review. Neurosurg Focus. 2009;27:E6.
doi: 10.3171/2009.8.FOCUS09150
Park P, Wang AC, Sangala JR, Kim SM, Hervey-Jumper S, Than KD, Farokhrani A, LaMarca F. Impact of multimodal intraoperative monitoring during correction of symptomatic cervical or cervicothoracic kyphosis. J Neurosurg Spine. 2011;14:99–105.
doi: 10.3171/2010.9.SPINE1085
Sloan TB, Heyer EJ. Anesthesia for intraoperative neurophysiologic monitoring of the spinal cord. J Clin Neurophysiol. 2002;19:430–43.
doi: 10.1097/00004691-200210000-00006
Haghighi SS, Green KD, Oro JJ, Drake RK, Kracke GR. Depressive effect of isoflurane anesthesia on motor evoked potentials. Neurosurgery. 1990;26:993–7.
doi: 10.1227/00006123-199006000-00012
Kalkman CJ, Drummond JC, Ribberink AA, Patel PM, Sano T, Bickford RG. Effects of propofol, etomidate, midazolam, and fentanyl on motor evoked responses to transcranial electrical or magnetic stimulation in humans. Anesthesiology. 1992;76:502–9.
doi: 10.1097/00000542-199204000-00003
Haghighi SS, Sirintrapun SJ, Keller BP, Oro JJ, Madsen R. Effect of desflurane anesthesia on transcortical motor evoked potentials. J Neurosurg Anesthesiol. 1996;8:47–51.
doi: 10.1097/00008506-199601000-00011
Kawaguchi M, Inoue S, Kakimoto M, Kitaguchi K, Furuya H, Morimoto T, Sakaki T. The effect of sevoflurane on myogenic motor-evoked potentials induced by single and paired transcranial electrical stimulation of the motor cortex during nitrous xide/ketamine/fentanyl anesthesia. J Neurosurg Anesthesiol. 1998;10:131–6.
doi: 10.1097/00008506-199807000-00001
Nathan N, Tabaraud F, Lacroix F, Mouliès D, Viviand X, Lansade A, Terrier G, Feiss P. Influence of propofol concentrations on multipulse transcranial motor evoked potentials. Br J Anaesth. 2003;91:493–7.
doi: 10.1093/bja/aeg211
Furutani K, Deguchi H, Matsuhashi M, Mitsuma Y, Kamiya Y, Baba H. A bolus dose of ketamine reduces the amplitude of the transcranial electrical motor-evoked potential: a randomized, double-blinded, placebo-controlled study. J Neurosurg Anesthesiol. 2019. https://doi.org/10.1097/ana.0000000000000653 (in press, Epub ahead of print).
doi: 10.1097/ana.0000000000000653 pubmed: 31633576
Deguchi H, Furutani K, Mitsuma Y, Kamiya Y, Baba H. Low-dose droperidol suppresses transcranial electrical motor-evoked potential amplitude: a retrospective study. J Clin Monit Comput. 2021;35:175–81.
doi: 10.1007/s10877-020-00464-4
Legatt AD, Emerson RG, Epstein CM, MacDonald DB, Deletis V, Bravo RJ, López JR. ACNS guideline: transcranial electrical stimulation motor evoked potential monitoring. J Clin Neurophysiol. 2016;33:42–50.
doi: 10.1097/WNP.0000000000000253
Concas A, Santoro G, Mascia MP, Serra M, Sanna E, Biggio G. The general anesthetic propofol enhances the function of gamma-aminobutyric acid-coupled chloride channel in the rat cerebral cortex. J Neurochem. 1990;55:2135–8.
doi: 10.1111/j.1471-4159.1990.tb05807.x
Hara M, Kai Y, Ikemoto Y. Propofol activates GABA
doi: 10.1097/00000542-199310000-00021
Grasshoff C, Antkowiak B. Propofol and sevoflurane depress spinal neurons in vitro via different molecular targets. Anesthesiology. 2004;101:1167–76.
doi: 10.1097/00000542-200411000-00017
Jin YH, Zhang Z, Mendelowitz D, Andresen MC. Presynaptic actions of propofol enhance inhibitory synaptic transmission in isolated solitary tract nucleus neurons. Brain Res. 2009;1286:75–83.
doi: 10.1016/j.brainres.2009.06.058
Baars J, Dangel C, Herold K, Hadzidiakos D, Rehberg B. Suppression of the human spinal H-reflex by propofol: a quantitative analysis. Acta Anaesthesiol Scand. 2006;50:193–200.
doi: 10.1111/j.1399-6576.2006.00923.x
Kammer T, Rehberg B, Menne D, Wartenberg H-C, Wenningmann I, Urban BW. Propofol and sevoflurane in subanesthetic concentrations act preferentially on the spinal cord: evidence from multimodal electrophysiological assessment. Anesthesiology. 2002;97:1416–25.
doi: 10.1097/00000542-200212000-00013
Kakinohana M, Fuchigami T, Nakamura S, Kawabata T, Sugahara K. Propofol reduces spinal motor neuron excitability in humans. Anesth Analg. 2002;94:1586–8.
pubmed: 12032032
Baars JH, von Dincklage F, Reiche J, Rehberg B. Propofol increases presynaptic inhibition of Ia afferents in the intact human spinal cord. Anesthesiology. 2006;104:798–804.
doi: 10.1097/00000542-200604000-00026
Kerz T, Hennes H-J, Fève A, Decq P, Filipetti P, Duvaldestin P. Effects of propofol on H-reflex in humans. Anesthesiology. 2001;94:32–7.
doi: 10.1097/00000542-200101000-00010
Kungys G, Kim J, Jinks SL, Atherley RJ, Antognini JF. Propofol produces immobility via action in the ventral horn of the spinal cord by a GABAergic mechanism. Anesth Analg. 2009;108:1531–7.
doi: 10.1213/ane.0b013e31819d9308
von Dincklage F, Reiche J, Rehberg B, Baars JH. H-reflex depression by propofol and sevoflurane is dependent on stimulus intensity. Clin Neurophysiol. 2006;117:2653–60.
doi: 10.1016/j.clinph.2006.08.006
Lawrence DG, Kuypers HG. The functional organization of the motor system in the monkey. I. The effects of bilateral pyramidal lesions. Brain. 1968;91:1–14.
doi: 10.1093/brain/91.1.1
Lawrence DG, Kuypers HG. The functional organization of the motor system in the monkey. II. The effects of lesions of the descending brain-stem pathways. Brain. 1968;91:15–36.
doi: 10.1093/brain/91.1.15
Lemon RN, Landau W, Tutssel D, Lawrence DG. Lawrence and Kuypers (1968a, b) revisited: copies of the original filmed material from their classic papers in brain. Brain. 2012;135:2290–5.
doi: 10.1093/brain/aws037
Rathelot JA, Strick PL. Subdivisions of primary motor cortex based on cortico-motoneuronal cells. Proc Natl Acad Sci USA. 2009;106:918–23.
doi: 10.1073/pnas.0808362106
Lemon RN. Descending pathways in motor control. Annu Rev Neurosci. 2008;31:195–218.
doi: 10.1146/annurev.neuro.31.060407.125547
Ueno M, Nakamura Y, Li J, Gu Z, Niehaus J, Maezawa M, Crone SA, Goulding M, Baccei ML, Yoshida Y. Corticospinal circuits from the sensory and motor cortices differentially regulate skilled movements through distinct spinal interneurons. Cell Rep. 2018;23:1286–300.
doi: 10.1016/j.celrep.2018.03.137
Deletis V, Rodi Z, Amassian VE. Neurophysiological mechanisms underlying motor evoked potentials in anesthetized humans. Part 2. Relationship between epidurally and muscle recorded MEPs in man. Clin Neurophysiol. 2001;112:445–52.
doi: 10.1016/S1388-2457(00)00557-5
Leslie K, Clavisi O, Hargrove J. Target-controlled infusion versus manually-controlled infusion of propofol for general anaesthesia or sedation in adults. Cochrane Database Syst Rev. 2008;3:CD006059.
Ohashi M, Watanabe K, Furutani K, Hirano T, Katsumi K, Shoji H, Mizouchi T, Endo N. False-negative transcranial motor evoked potentials (TcMEPs) during surgery for congenital lumbar kyphoscoliosis: a case report. Spinal Cord Ser Cases. 2017;3:17053.
doi: 10.1038/scsandc.2017.53

Auteurs

Hiroyuki Deguchi (H)

Department of Anesthesiology, Niigata University Medical and Dental Hospital, 1-754 Asahimachi-Dori, Chuo-ku, Niigata, 951-8520, Japan.

Kenta Furutani (K)

Department of Anesthesiology, Niigata University Medical and Dental Hospital, 1-754 Asahimachi-Dori, Chuo-ku, Niigata, 951-8520, Japan. kenta-f@med.niigata-u.ac.jp.

Yusuke Mitsuma (Y)

Department of Anesthesiology, Niigata University Medical and Dental Hospital, 1-754 Asahimachi-Dori, Chuo-ku, Niigata, 951-8520, Japan.

Yoshinori Kamiya (Y)

Department of Anesthesiology, Niigata University Medical and Dental Hospital, 1-754 Asahimachi-Dori, Chuo-ku, Niigata, 951-8520, Japan.

Hiroshi Baba (H)

Department of Anesthesiology, Niigata University Medical and Dental Hospital, 1-754 Asahimachi-Dori, Chuo-ku, Niigata, 951-8520, Japan.

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