Original Article
Journal of Cerebral Blood Flow & Metabolism (2009) 29, 1035–1047; doi:10.1038/jcbfm.2009.7; published online 18 February 2009
Propofol anesthesia does not alter regional rates of cerebral protein synthesis measured with L-[1-11C]leucine and PET in healthy male subjects
This research was supported by the Intramural Research Program, National Institute of Mental Health; Clinical Center, National Institutes of Health; Fragile X Research Foundation.
Shrinivas Bishu1, Kathleen C Schmidt1, Thomas V Burlin1, Michael A Channing2, Lisa Horowitz3, Tianjiang Huang1, Zhong-hua Liu1, Mei Qin1, B-K Vuong2, Aaron J Unterman1, Zengyan Xia1, Alan Zametkin1, Peter Herscovitch2, Zenaide Quezado4 and Carolyn B Smith1
- 1Section on Neuroadaptation and Protein Metabolism, National Institute of Mental Health, Bethesda, Maryland, USA
- 2PET Department, National Institutes of Health Clinical Center, National Institutes of Health, Bethesda, Maryland, USA
- 3Office of the Clinical Director, National Institute of Mental Health, Bethesda, Maryland, USA
- 4Department of Anesthesia and Surgical Services, National Institutes of Health Clinical Center, National Institutes of Health, Bethesda, Maryland, USA
Correspondence: Dr S Bishu, Section on Neuroadaptation and Protein Metabolism, National Institute of Mental Health, Bldg 10, Rm 2D54, 10 Center Drive, Bethesda, MD 20892-1298, USA. E-mail: bishus@mail.nih.gov
Received 25 September 2008; Revised 7 January 2009; Accepted 8 January 2009; Published online 18 February 2009.
Abstract
We report regional rates of cerebral protein synthesis (rCPS) in 10 healthy young males, each studied under two conditions: awake and anesthetized with propofol. We used the quantitative L-[1-11C]leucine positron emission tomography (PET) method to measure rCPS. The method accounts for the fraction (
) of unlabeled leucine in the precursor pool for protein synthesis that is derived from arterial plasma; the remainder comes from proteolysis of tissue proteins. Across 18 regions and whole brain, mean differences in rCPS between studies ranged from -5% to 5% and were within the variability of rCPS in awake studies (coefficient of variation range: 7% to 14%). Similarly, differences in
(range: 1% to 4%) were typically within the variability of
(coefficient of variation range: 3% to 6%). Intersubject variances and patterns of regional variation were also similar under both conditions. In propofol-anesthetized subjects, rCPS varied regionally from 0.98
0.12 to 2.39
0.23 nmol g-1 min-1 in the corona radiata and in the cerebellum, respectively. Our data indicate that the values, variances, and patterns of regional variation in rCPS and
measured by the L-[1-11C]leucine PET method are not significantly altered by anesthesia with propofol.
Keywords:
anesthesia, brain, human, propofol, protein synthesis, positron emission tomography
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