Sevoflurane 0.25 MAC Preferentially Affects Higher Order Association Areas: A Functional Magnetic Resonance Imaging Study in Volunteers

BACKGROUND:Functional magnetic resonance imaging (fMRI) can objectively measure the subjective effects of anesthesia. Memory-related regions (association areas) are affected by subanesthetic doses of volatile anesthetics. In this study we measured the regional neuronal effects of 0.25 MAC sevoflurane in healthy volunteers and differentiated the effect between primary cortical regions and association areas. METHODS:The effect of 0.25 MAC sevoflurane on visual, auditory, and motor activation was studied in 16 ASA I volunteers. With fMRI (3 Tesla Siemens magnetom), regional cerebral blood flow (rCBF) was measured by the pulsed arterial spin labeling technique. Subjects inhaled a mixture of O2 and 0.25 MAC sevoflurane and standard ASA monitoring was performed. Visual, auditory, and motor activation tasks were used. rCBF was measured in the awake state and during inhalation of 0.25 MAC sevoflurane, without and with activation. The change in rCBF (&dgr;CBF) with 0.25 MAC Sevoflurane during baseline state and with activation was calculated in 11 regions of interest related to visual, auditory, and motor activation tasks. RESULTS:The change from baseline rCBF with 0.25 MAC sevoflurane was not statistically significant in the 11 regions of interest. With activation there was a significant increase in CBF in several regions. However, only in the primary and secondary visual cortices (V1, V2), thalamus, hippocampus, and supplementary motor area was the decrease in activation with 0.25 MAC sevoflurane statistically significant (P < 0.05). CONCLUSION:Memory-related regions (association areas) are affected by subanesthetic concentrations of volatile anesthetics. Using fMRI, this study showed that 0.25 MAC sevoflurane predominantly affects the primary visual cortex, the related association cortex, and certain other higher order association cortices.

[1]  E. G. Jones,et al.  Numbers and proportions of GABA-immunoreactive neurons in different areas of monkey cerebral cortex , 1987, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[2]  Gary H. Glover,et al.  Assessment of Hemodynamic Response during Focal Neural Activity in Human Using Bolus Tracking, Arterial Spin Labeling and BOLD Techniques , 2000, NeuroImage.

[3]  A. Gjedde,et al.  Effects of subanaesthetic and anaesthetic doses of sevoflurane on regional cerebral blood flow in healthy volunteers. A positron emission tomographic study , 2004, Acta anaesthesiologica Scandinavica.

[4]  Jeff Duyn,et al.  H215O PET validation of steady‐state arterial spin tagging cerebral blood flow measurements in humans , 2000, Magnetic resonance in medicine.

[5]  T. Kazama,et al.  Influence of Age on Awakening Concentrations of Sevoflurane and Isoflurane , 1993, Anesthesia and analgesia.

[6]  B. Orser,et al.  Inhaled Anesthetics and Immobility: Mechanisms, Mysteries, and Minimum Alveolar Anesthetic Concentration , 2003, Anesthesia and analgesia.

[7]  E C Wong,et al.  Magnetic resonance imaging of human brain function. Principles, practicalities, and possibilities. , 1997, Neurosurgery clinics of North America.

[8]  M. Renna,et al.  The effect of sevoflurane on implicit memory: a double‐blind, randomised study , 2000, Anaesthesia.

[9]  D. Chernik,et al.  Validity and Reliability of the Observer's: Assessment of Alertness/Sedation Scale Study with Intravenous Midazolam , 1990, Journal of clinical psychopharmacology.

[10]  Yihong Yang,et al.  Perfusion MR Imaging with pulsed arterial spin-labeling: basic priciples and applications in functional brain imaging , 2002 .

[11]  C. Schwarzbauer,et al.  Subanesthetic Isoflurane Affects Task-induced Brain Activation in a Highly Specific Manner: A Functional Magnetic Resonance Imaging Study , 2001, Anesthesiology.

[12]  Alan C. Evans,et al.  Brain Mechanisms of Propofol-Induced Loss of Consciousness in Humans: a Positron Emission Tomographic Study , 1999, The Journal of Neuroscience.

[13]  B. Rosner,et al.  Neural Effects of Isoflurane (Forane) in Man , 1973, Anesthesiology.

[14]  N. Logothetis,et al.  Neurophysiological investigation of the basis of the fMRI signal , 2001, Nature.

[15]  M. Torrens Co-Planar Stereotaxic Atlas of the Human Brain—3-Dimensional Proportional System: An Approach to Cerebral Imaging, J. Talairach, P. Tournoux. Georg Thieme Verlag, New York (1988), 122 pp., 130 figs. DM 268 , 1990 .

[16]  X. Golay,et al.  Perfusion Imaging Using Arterial Spin Labeling , 2004, Topics in magnetic resonance imaging : TMRI.

[17]  C. Schwarzbauer,et al.  In vivo imaging of anaesthetic action in humans: approaches with positron emission tomography (PET) and functional magnetic resonance imaging (fMRI). , 2002, British journal of anaesthesia.

[18]  V. Feshchenko,et al.  A Neuroanatomical Construct for the Amnesic Effects of Propofol , 2002, Anesthesiology.

[19]  J. Dilger,et al.  The effects of general anaesthetics on ligand-gated ion channels. , 2002, British journal of anaesthesia.

[20]  J. Mazziotta,et al.  METABOLIC MAPPING OF THE BRAIN'S RESPONSE TO VISUAL STIMULATION: STUDIES IN HUMANS , 1981, Science.

[21]  K. Miller,et al.  Mechanisms of actions of inhaled anesthetics. , 2003, The New England journal of medicine.

[22]  A Baddeley,et al.  A measure of consciousness and memory during isoflurane administration: the coherent frequency. , 1994, British journal of anaesthesia.

[23]  C Prys-Roberts,et al.  Anaesthesia: a practical or impractical construct? , 1987, British Journal of Anaesthesia.

[24]  M E Moseley,et al.  Quantification of cerebral blood flow by bolus tracking and artery spin tagging methods. , 2000, Magnetic resonance imaging.