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Front Syst Neurosci. 2017 Sep 14;11:66. doi: 10.3389/fnsys.2017.00066. eCollection 2017.

Brainstem Influence on Thalamocortical Oscillations during Anesthesia Emergence.

Frontiers in systems neuroscience

Christopher M Scheib

Affiliations

  1. Anesthesia Department, W. G. (Bill) Hefner VA Medical CenterSalisbury, NC, United States.

PMID: 28959192 PMCID: PMC5603712 DOI: 10.3389/fnsys.2017.00066

Abstract

Theories of mechanisms that impair or prevent consciousness during anesthesia that are related to thalamocortical oscillations have been proposed. Many methods of EEG analysis have been proposed as measures of anesthetic effects but only a few have potential to provide measures of those anesthetic effects that are directly related to thalamocortical oscillations. Some of these methods will be explained and demonstrated with examples chosen to provide evidence for or against two of the proposed mechanisms. The first of the two mechanisms to be addressed is the "traveling peak" (Ching et al., 2010), which relates to anesthetic agents synchronizing neural oscillations that occur in subjects who are awake and reducing their frequency from the gamma (25-40 Hz) to the beta range (13-24 Hz) as a state of sedation develops. The mechanism continues to lower the frequency of this oscillation to the alpha (8-12 Hz) range. In the alpha frequency range, responses to sounds and words stop. It has been proposed that the mechanism changes fundamentally at this point and the oscillations are not compatible with consciousness. The second mechanism that will be addressed is a modification of the generally accepted mechanism for the spindle oscillations that occur during natural sleep (Steriade et al., 1993a,b). These two different mechanisms imply two different patterns for changes in the frequency of the thalamocortical oscillations during emergence. The first mechanism implies that the frequency of the oscillations should increase from the alpha range to the beta range during emergence. The "spindle" mechanism implies that the frequency of the oscillation would not increase much beyond the alpha range. Examples of EEG recordings during anesthesia and emergence from anesthesia were found which were consistent with either mechanism alone or both mechanisms at the same time. Neither theory was able to explain all examples. It is possible that both mechanisms can occur and that brainstem activity may influence the characteristics of emergence. The brainstem activity in question may be influenced by nociception and analgesic supplementation. It may be possible to control the path of emergence by controlling brainstem activity with opioids and other agents in order to allow the patient to awaken without going through an excitement phase or delirium at the transition to consciousness.

Keywords: EEG; anesthesia; brainstem; electroencephalogram; emergence; spectrum; spindles; thalamus

References

  1. Curr Biol. 2012 Nov 6;22(21):2008-16 - PubMed
  2. Cell Calcium. 2006 Aug;40(2):175-90 - PubMed
  3. J Neurosci. 2014 Dec 3;34(49):16385-96 - PubMed
  4. Nature. 2005 Oct 27;437(7063):1257-63 - PubMed
  5. Anesthesiology. 2005 Feb;102(2):447-71 - PubMed
  6. Brain Res. 2011 Dec 2;1426:30-7 - PubMed
  7. Anesthesiology. 2015 Oct;123(4):937-60 - PubMed
  8. J Neurophysiol. 1987 Jan;57(1):260-73 - PubMed
  9. Anesthesiology. 1999 Jan;90(1):120-34 - PubMed
  10. Science. 1993 Oct 29;262(5134):679-85 - PubMed
  11. Anesth Analg. 2009 Aug;109(2):539-50 - PubMed
  12. Anesthesiology. 2014 Oct;121(4):740-52 - PubMed
  13. Science. 1935 Jun 14;81(2111):597-8 - PubMed
  14. Annu Rev Neurosci. 1997;20:185-215 - PubMed
  15. Br J Anaesth. 2007 Oct;99(4):532-7 - PubMed
  16. Proc Natl Acad Sci U S A. 2013 Mar 19;110(12):E1142-51 - PubMed
  17. Science. 2008 Nov 7;322(5903):876-80 - PubMed
  18. Anesthesiology. 1998 Aug;89(2):323-33 - PubMed
  19. Proc Natl Acad Sci U S A. 1993 Mar 1;90(5):2078-81 - PubMed
  20. J Comp Neurol. 2008 Jun 1;508(4):648-62 - PubMed
  21. J Pharmacol Exp Ther. 2005 Nov;315(2):517-25 - PubMed
  22. Anesthesiology. 1998 Oct;89(4):980-1002 - PubMed
  23. Trends Neurosci. 1989 Jun;12(6):215-21 - PubMed
  24. Prog Brain Res. 1991;88:293-305 - PubMed
  25. J Neurophysiol. 2001 Jul;86(1):1-39 - PubMed
  26. Eur J Neurosci. 2006 Jan;23(2):465-80 - PubMed
  27. Nat Rev Neurosci. 2008 May;9(5):370-86 - PubMed
  28. PLoS One. 2014 Sep 29;9(9):e106291 - PubMed
  29. Anesthesiology. 2009 Dec;111(6):1271-8 - PubMed
  30. Anesthesiology. 2013 Jan;118(1):13-5 - PubMed
  31. Curr Pharm Des. 2006;12(28):3665-79 - PubMed
  32. Anesthesiology. 2009 Sep;111(3):547-55 - PubMed
  33. Neuron. 1998 Jul;21(1):9-12 - PubMed
  34. Front Syst Neurosci. 2014 Aug 13;8:146 - PubMed
  35. J Biol Rhythms. 2006 Dec;21(6):482-93 - PubMed
  36. J Vis Exp. 2013 Oct 16;(80):e51079 - PubMed
  37. J Neurophysiol. 1985 Dec;54(6):1473-97 - PubMed
  38. Proc Natl Acad Sci U S A. 2010 Dec 28;107(52):22665-70 - PubMed
  39. J Neurophysiol. 2005 Apr;93(4):2194-232 - PubMed
  40. N Engl J Med. 2003 May 22;348(21):2110-24 - PubMed
  41. J Neurophysiol. 1998 Feb;79(2):999-1016 - PubMed
  42. J Neurosci. 2013 Jul 3;33(27):11070-5 - PubMed
  43. J Neurosci. 1993 Aug;13(8):3284-99 - PubMed

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