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Plasma Lipid Profiles Change with Increasing Numbers of Mild Traumatic Brain Injuries in Rats

Mild traumatic brain injury (mTBI) causes structural, cellular and biochemical alterations which are difficult to detect in the brain and may persist chronically following single or repeated injury. Lipids are abundant in the brain and readily cross the blood-brain barrier, suggesting that lipidomic...

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Autores principales: Anyaegbu, Chidozie C., Szemray, Harrison, Hellewell, Sarah C., Lawler, Nathan G., Leggett, Kerry, Bartlett, Carole, Lins, Brittney, McGonigle, Terence, Papini, Melissa, Anderton, Ryan S., Whiley, Luke, Fitzgerald, Melinda
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9025508/
https://www.ncbi.nlm.nih.gov/pubmed/35448509
http://dx.doi.org/10.3390/metabo12040322
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author Anyaegbu, Chidozie C.
Szemray, Harrison
Hellewell, Sarah C.
Lawler, Nathan G.
Leggett, Kerry
Bartlett, Carole
Lins, Brittney
McGonigle, Terence
Papini, Melissa
Anderton, Ryan S.
Whiley, Luke
Fitzgerald, Melinda
author_facet Anyaegbu, Chidozie C.
Szemray, Harrison
Hellewell, Sarah C.
Lawler, Nathan G.
Leggett, Kerry
Bartlett, Carole
Lins, Brittney
McGonigle, Terence
Papini, Melissa
Anderton, Ryan S.
Whiley, Luke
Fitzgerald, Melinda
author_sort Anyaegbu, Chidozie C.
collection PubMed
description Mild traumatic brain injury (mTBI) causes structural, cellular and biochemical alterations which are difficult to detect in the brain and may persist chronically following single or repeated injury. Lipids are abundant in the brain and readily cross the blood-brain barrier, suggesting that lipidomic analysis of blood samples may provide valuable insight into the neuropathological state. This study used liquid chromatography-mass spectrometry (LC-MS) to examine plasma lipid concentrations at 11 days following sham (no injury), one (1×) or two (2×) mTBI in rats. Eighteen lipid species were identified that distinguished between sham, 1× and 2× mTBI. Three distinct patterns were found: (1) lipids that were altered significantly in concentration after either 1× or 2× F mTBI: cholesterol ester CE (14:0) (increased), phosphoserine PS (14:0/18:2) and hexosylceramide HCER (d18:0/26:0) (decreased), phosphoinositol PI(16:0/18:2) (increased with 1×, decreased with 2× mTBI); (2) lipids that were altered in response to 1× mTBI only: free fatty acid FFA (18:3 and 20:3) (increased); (3) lipids that were altered in response to 2× mTBI only: HCER (22:0), phosphoethanolamine PE (P-18:1/20:4 and P-18:0/20:1) (increased), lysophosphatidylethanolamine LPE (20:1), phosphocholine PC (20:0/22:4), PI (18:1/18:2 and 20:0/18:2) (decreased). These findings suggest that increasing numbers of mTBI induce a range of changes dependent upon the lipid species, which likely reflect a balance of damage and reparative responses.
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spelling pubmed-90255082022-04-23 Plasma Lipid Profiles Change with Increasing Numbers of Mild Traumatic Brain Injuries in Rats Anyaegbu, Chidozie C. Szemray, Harrison Hellewell, Sarah C. Lawler, Nathan G. Leggett, Kerry Bartlett, Carole Lins, Brittney McGonigle, Terence Papini, Melissa Anderton, Ryan S. Whiley, Luke Fitzgerald, Melinda Metabolites Article Mild traumatic brain injury (mTBI) causes structural, cellular and biochemical alterations which are difficult to detect in the brain and may persist chronically following single or repeated injury. Lipids are abundant in the brain and readily cross the blood-brain barrier, suggesting that lipidomic analysis of blood samples may provide valuable insight into the neuropathological state. This study used liquid chromatography-mass spectrometry (LC-MS) to examine plasma lipid concentrations at 11 days following sham (no injury), one (1×) or two (2×) mTBI in rats. Eighteen lipid species were identified that distinguished between sham, 1× and 2× mTBI. Three distinct patterns were found: (1) lipids that were altered significantly in concentration after either 1× or 2× F mTBI: cholesterol ester CE (14:0) (increased), phosphoserine PS (14:0/18:2) and hexosylceramide HCER (d18:0/26:0) (decreased), phosphoinositol PI(16:0/18:2) (increased with 1×, decreased with 2× mTBI); (2) lipids that were altered in response to 1× mTBI only: free fatty acid FFA (18:3 and 20:3) (increased); (3) lipids that were altered in response to 2× mTBI only: HCER (22:0), phosphoethanolamine PE (P-18:1/20:4 and P-18:0/20:1) (increased), lysophosphatidylethanolamine LPE (20:1), phosphocholine PC (20:0/22:4), PI (18:1/18:2 and 20:0/18:2) (decreased). These findings suggest that increasing numbers of mTBI induce a range of changes dependent upon the lipid species, which likely reflect a balance of damage and reparative responses. MDPI 2022-04-02 /pmc/articles/PMC9025508/ /pubmed/35448509 http://dx.doi.org/10.3390/metabo12040322 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Anyaegbu, Chidozie C.
Szemray, Harrison
Hellewell, Sarah C.
Lawler, Nathan G.
Leggett, Kerry
Bartlett, Carole
Lins, Brittney
McGonigle, Terence
Papini, Melissa
Anderton, Ryan S.
Whiley, Luke
Fitzgerald, Melinda
Plasma Lipid Profiles Change with Increasing Numbers of Mild Traumatic Brain Injuries in Rats
title Plasma Lipid Profiles Change with Increasing Numbers of Mild Traumatic Brain Injuries in Rats
title_full Plasma Lipid Profiles Change with Increasing Numbers of Mild Traumatic Brain Injuries in Rats
title_fullStr Plasma Lipid Profiles Change with Increasing Numbers of Mild Traumatic Brain Injuries in Rats
title_full_unstemmed Plasma Lipid Profiles Change with Increasing Numbers of Mild Traumatic Brain Injuries in Rats
title_short Plasma Lipid Profiles Change with Increasing Numbers of Mild Traumatic Brain Injuries in Rats
title_sort plasma lipid profiles change with increasing numbers of mild traumatic brain injuries in rats
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9025508/
https://www.ncbi.nlm.nih.gov/pubmed/35448509
http://dx.doi.org/10.3390/metabo12040322
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