Membrane depolarization and aberrant lipid distributions in the neonatal rat brain following hypoxic-ischaemic insult

Abstract Neonatal hypoxic-ischaemic (HI) encephalopathy is among the most serious complications in neonatology. In the present study, we studied the immediate (0 hour), subacute (36 hours) and late (144 hours) responses of the neonatal brain to experimental HI insult in laboratory rats. At the stria...

Full description

Bibliographic Details
Main Authors: Dominika Luptakova, Ladislav Baciak, Tomas Pluhacek, Anton Skriba, Blanka Sediva, Vladimir Havlicek, Ivo Juranek
Format: Article
Language:English
Published: Nature Portfolio 2018-05-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-018-25088-2
_version_ 1818998810350714880
author Dominika Luptakova
Ladislav Baciak
Tomas Pluhacek
Anton Skriba
Blanka Sediva
Vladimir Havlicek
Ivo Juranek
author_facet Dominika Luptakova
Ladislav Baciak
Tomas Pluhacek
Anton Skriba
Blanka Sediva
Vladimir Havlicek
Ivo Juranek
author_sort Dominika Luptakova
collection DOAJ
description Abstract Neonatal hypoxic-ischaemic (HI) encephalopathy is among the most serious complications in neonatology. In the present study, we studied the immediate (0 hour), subacute (36 hours) and late (144 hours) responses of the neonatal brain to experimental HI insult in laboratory rats. At the striatal level, the mass spectrometry imaging revealed an aberrant plasma membrane distribution of Na+/K+ ions in the oedema-affected areas. The failure of the Na+/K+ gradients was also apparent in the magnetic resonance imaging measurements, demonstrating intracellular water accumulation during the acute phase of the HI insult. During the subacute phase, compared with the control brains, an incipient accumulation of an array of N-acylphosphatidylethanolamine (NAPE) molecules was detected in the HI-affected brains, and both the cytotoxic and vasogenic types of oedema were detected. In the severely affected brain areas, abnormal distributions of the monosialogangliosides GM2 and GM3 were observed in two-thirds of the animals exposed to the insult. During the late stage, a partial restoration of the brain tissue was observed in most rats in both the in vivo and ex vivo studies. These specific molecular changes may be further utilized in neonatology practice in proposing and testing novel therapeutic strategies for the treatment of neonatal HI encephalopathy.
first_indexed 2024-12-20T22:07:26Z
format Article
id doaj.art-4b9726728d1547239d5aa7c67427ce46
institution Directory Open Access Journal
issn 2045-2322
language English
last_indexed 2024-12-20T22:07:26Z
publishDate 2018-05-01
publisher Nature Portfolio
record_format Article
series Scientific Reports
spelling doaj.art-4b9726728d1547239d5aa7c67427ce462022-12-21T19:25:14ZengNature PortfolioScientific Reports2045-23222018-05-018111110.1038/s41598-018-25088-2Membrane depolarization and aberrant lipid distributions in the neonatal rat brain following hypoxic-ischaemic insultDominika Luptakova0Ladislav Baciak1Tomas Pluhacek2Anton Skriba3Blanka Sediva4Vladimir Havlicek5Ivo Juranek6Institute of Microbiology of the Czech Academy of SciencesInstitute of Experimental Pharmacology and Toxicology, CEM of the SASInstitute of Microbiology of the Czech Academy of SciencesInstitute of Microbiology of the Czech Academy of SciencesInstitute of Microbiology of the Czech Academy of SciencesInstitute of Microbiology of the Czech Academy of SciencesInstitute of Experimental Pharmacology and Toxicology, CEM of the SASAbstract Neonatal hypoxic-ischaemic (HI) encephalopathy is among the most serious complications in neonatology. In the present study, we studied the immediate (0 hour), subacute (36 hours) and late (144 hours) responses of the neonatal brain to experimental HI insult in laboratory rats. At the striatal level, the mass spectrometry imaging revealed an aberrant plasma membrane distribution of Na+/K+ ions in the oedema-affected areas. The failure of the Na+/K+ gradients was also apparent in the magnetic resonance imaging measurements, demonstrating intracellular water accumulation during the acute phase of the HI insult. During the subacute phase, compared with the control brains, an incipient accumulation of an array of N-acylphosphatidylethanolamine (NAPE) molecules was detected in the HI-affected brains, and both the cytotoxic and vasogenic types of oedema were detected. In the severely affected brain areas, abnormal distributions of the monosialogangliosides GM2 and GM3 were observed in two-thirds of the animals exposed to the insult. During the late stage, a partial restoration of the brain tissue was observed in most rats in both the in vivo and ex vivo studies. These specific molecular changes may be further utilized in neonatology practice in proposing and testing novel therapeutic strategies for the treatment of neonatal HI encephalopathy.https://doi.org/10.1038/s41598-018-25088-2
spellingShingle Dominika Luptakova
Ladislav Baciak
Tomas Pluhacek
Anton Skriba
Blanka Sediva
Vladimir Havlicek
Ivo Juranek
Membrane depolarization and aberrant lipid distributions in the neonatal rat brain following hypoxic-ischaemic insult
Scientific Reports
title Membrane depolarization and aberrant lipid distributions in the neonatal rat brain following hypoxic-ischaemic insult
title_full Membrane depolarization and aberrant lipid distributions in the neonatal rat brain following hypoxic-ischaemic insult
title_fullStr Membrane depolarization and aberrant lipid distributions in the neonatal rat brain following hypoxic-ischaemic insult
title_full_unstemmed Membrane depolarization and aberrant lipid distributions in the neonatal rat brain following hypoxic-ischaemic insult
title_short Membrane depolarization and aberrant lipid distributions in the neonatal rat brain following hypoxic-ischaemic insult
title_sort membrane depolarization and aberrant lipid distributions in the neonatal rat brain following hypoxic ischaemic insult
url https://doi.org/10.1038/s41598-018-25088-2
work_keys_str_mv AT dominikaluptakova membranedepolarizationandaberrantlipiddistributionsintheneonatalratbrainfollowinghypoxicischaemicinsult
AT ladislavbaciak membranedepolarizationandaberrantlipiddistributionsintheneonatalratbrainfollowinghypoxicischaemicinsult
AT tomaspluhacek membranedepolarizationandaberrantlipiddistributionsintheneonatalratbrainfollowinghypoxicischaemicinsult
AT antonskriba membranedepolarizationandaberrantlipiddistributionsintheneonatalratbrainfollowinghypoxicischaemicinsult
AT blankasediva membranedepolarizationandaberrantlipiddistributionsintheneonatalratbrainfollowinghypoxicischaemicinsult
AT vladimirhavlicek membranedepolarizationandaberrantlipiddistributionsintheneonatalratbrainfollowinghypoxicischaemicinsult
AT ivojuranek membranedepolarizationandaberrantlipiddistributionsintheneonatalratbrainfollowinghypoxicischaemicinsult