Literature DB >> 22189890

Changes in plasma phenylalanine, isoleucine, leucine, and valine are associated with significant changes in intracranial pressure and jugular venous oxygen saturation in patients with severe traumatic brain injury.

Raphael N Vuille-Dit-Bille1, Riem Ha-Huy, John F Stover.   

Abstract

Changes in plasma aromatic amino acids (AAA = phenylalanine, tryptophan, tyrosine) and branched chain amino acids (BCAA = isoleucine, leucine, valine) levels possibly influencing intracranial pressure (ICP) and cerebral oxygen consumption (SjvO(2)) were investigated in 19 sedated patients up to 14 days following severe traumatic brain injury (TBI). Compared to 44 healthy volunteers, jugular venous plasma BCAA were significantly decreased by 35% (p < 0.001) while AAA were markedly increased in TBI patients by 19% (p < 0.001). The BCAA to AAA ratio was significantly decreased by 55% (p < 0.001) which persisted during the entire study period. Elevated plasma phenylalanine was associated with decreased ICP and increased SjvO(2), while higher plasma isoleucine and leucine levels were associated with increased ICP and higher plasma leucine and valine were linked to decreased SjvO(2). The amount of enterally administered amino acids was associated with significantly increased plasma levels with the exception of phenylalanine. Contrary to the initial assumption that elevated AAA and decreased BCAA levels are detrimental, increased plasma phenylalanine levels were associated with beneficial signs in terms of decreased ICP and reduced cerebral oxygen consumption reflected by increased SjvO(2); concomitantly, elevated plasma isoleucine and leucine levels were associated with increased ICP while leucine and valine were associated with decreased SjvO(2) following severe TBI, respectively. The impact of enteral nutrition on this observed pattern must be examined prospectively to determine if higher amounts of phenylalanine should be administered to promote beneficial effects on brain metabolism and if normalization of plasma BCAA levels is without cerebral side effects.

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Year:  2011        PMID: 22189890     DOI: 10.1007/s00726-011-1202-x

Source DB:  PubMed          Journal:  Amino Acids        ISSN: 0939-4451            Impact factor:   3.520


  11 in total

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Journal:  Exp Neurol       Date:  2019-04-03       Impact factor: 5.330

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Journal:  J Neurotrauma       Date:  2018-07-11       Impact factor: 5.269

Review 4.  Divergent Metabolic Regulation of Autophagy and mTORC1-Early Events in Alzheimer's Disease?

Authors:  Mai A Shafei; Matthew Harris; Myra E Conway
Journal:  Front Aging Neurosci       Date:  2017-06-02       Impact factor: 5.750

5.  Discovery and validation of temporal patterns involved in human brain ketometabolism in cerebral microdialysis fluids of traumatic brain injury patients.

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6.  Severe Spinal Cord Injury in Rats Induces Chronic Changes in the Spinal Cord and Cerebral Cortex Metabolism, Adjusted by Thiamine That Improves Locomotor Performance.

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Journal:  Front Pharmacol       Date:  2021-04-16       Impact factor: 5.810

8.  Traumatic Brain Injury Alters Methionine Metabolism: Implications for Pathophysiology.

Authors:  Pramod K Dash; Georgene W Hergenroeder; Cameron B Jeter; H Alex Choi; Nobuhide Kobori; Anthony N Moore
Journal:  Front Syst Neurosci       Date:  2016-04-29

9.  VISSA-PLS-DA-Based Metabolomics Reveals a Multitargeted Mechanism of Traditional Chinese Medicine for Traumatic Brain Injury.

Authors:  Zian Xia; Wenbin Liu; Fei Zheng; Wei Huang; Zhihua Xing; Weijun Peng; Tao Tang; Jiekun Luo; Lunzhao Yi; Yang Wang
Journal:  ASN Neuro       Date:  2020 Jan-Dec       Impact factor: 4.146

Review 10.  Alzheimer's disease: targeting the glutamatergic system.

Authors:  Myra E Conway
Journal:  Biogerontology       Date:  2020-02-11       Impact factor: 4.277

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