Literature DB >> 18829594

Cerebrospinal fluid phospholipid changes following traumatic brain injury.

Alice E Pasvogel1, Petra Miketova, Ida M Ki Moore.   

Abstract

Traumatic brain injury (TBI) is a leading cause of morbidity and mortality, with approximately 1.4 million people suffering a TBI each year. With TBI, a cascade of events is initiated including the activation of phospholipases, which leads to the disruption of the lipid bilayer of the membrane of neurons and neuroglia. The purpose of this study is to describe phospholipid changes following TBI. A total of 39 cerebrospinal fluid samples were obtained from the ventricular catheter system of 10 participants who received a TBI as a result of a motor vehicle crash, being struck by a vehicle as a pedestrian, or a fall. Phospholipids were extracted from samples and measured by normal-phase high-performance liquid chromatography with ultraviolet detector at a wavelength of 206 nm. The highest mean concentration of lysophosphatidylcholine occurred on Day 1 after injury. The concentration of phosphatidylserine was variable, with the highest mean concentration occurring on Day 2 after injury. The highest mean concentrations of phosphatidylethanolamine, phosphatidylcholine, and sphingomyelin occurred on Day 4 after injury. Findings provide preliminary evidence for disruption of central nervous system membrane phospholipids following TBI.

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Year:  2008        PMID: 18829594     DOI: 10.1177/1099800408323218

Source DB:  PubMed          Journal:  Biol Res Nurs        ISSN: 1099-8004            Impact factor:   2.522


  8 in total

1.  Discovery of Lipidome Alterations Following Traumatic Brain Injury via High-Resolution Metabolomics.

Authors:  Scott R Hogan; John H Phan; Melissa Alvarado-Velez; May Dongmei Wang; Ravi V Bellamkonda; Facundo M Fernández; Michelle C LaPlaca
Journal:  J Proteome Res       Date:  2018-04-27       Impact factor: 4.466

2.  Plasma metabolomic biomarkers accurately classify acute mild traumatic brain injury from controls.

Authors:  Massimo S Fiandaca; Mark Mapstone; Amin Mahmoodi; Thomas Gross; Fabio Macciardi; Amrita K Cheema; Kian Merchant-Borna; Jeffrey Bazarian; Howard J Federoff
Journal:  PLoS One       Date:  2018-04-20       Impact factor: 3.240

3.  LPA1 , LPA2 , LPA4 , and LPA6 receptor expression during mouse brain development.

Authors:  Olga Suckau; Isabel Gross; Sandra Schrötter; Fan Yang; Jiankai Luo; Andreas Wree; Jerold Chun; David Baska; Jan Baumgart; Kuniyuki Kano; Junken Aoki; Anja U Bräuer
Journal:  Dev Dyn       Date:  2019-03-27       Impact factor: 3.780

Review 4.  DAMPs and RAGE Pathophysiology at the Acute Phase of Brain Injury: An Overview.

Authors:  Baptiste Balança; Laurent Desmurs; Jérémy Grelier; Armand Perret-Liaudet; Anne-Claire Lukaszewicz
Journal:  Int J Mol Sci       Date:  2021-02-28       Impact factor: 5.923

5.  Metabolic Abnormalities in Patients with Chronic Disorders of Consciousness.

Authors:  Jie Yu; Fanxia Meng; Fangping He; Fei Chen; Wangxiao Bao; Yamei Yu; Jintao Zhou; Jian Gao; Jingqi Li; Yao Yao; Woo-Ping Ge; Benyan Luo
Journal:  Aging Dis       Date:  2021-04-01       Impact factor: 6.745

6.  Lipidome Alterations following Mild Traumatic Brain Injury in the Rat.

Authors:  Eric C Gier; Alexis N Pulliam; David A Gaul; Samuel G Moore; Michelle C LaPlaca; Facundo M Fernández
Journal:  Metabolites       Date:  2022-02-05

7.  Plasma Phospholipid Metabolites Associate With Functional Outcomes Following Mild Traumatic Brain Injury in Older Adults.

Authors:  Sarah R Martha; Kuan-Fu Chen; Yvonne Lin; Hilaire J Thompson
Journal:  Biol Res Nurs       Date:  2020-07-22       Impact factor: 2.522

8.  Zika virus infection modulates the metabolomic profile of microglial cells.

Authors:  Fodé Diop; Thomas Vial; Pauline Ferraris; Sineewanlaya Wichit; Michèle Bengue; Rodolphe Hamel; Loïc Talignani; Florian Liegeois; Julien Pompon; Hans Yssel; Guillaume Marti; Dorothée Missé
Journal:  PLoS One       Date:  2018-10-25       Impact factor: 3.240

  8 in total

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