SwePub
Sök i LIBRIS databas

  Extended search

WFRF:(Bührer Christoph)
 

Search: WFRF:(Bührer Christoph) > (2012) > Interaction of infl...

  • 1 of 1
  • Previous record
  • Next record
  •    To hitlist

Interaction of inflammation and hyperoxia in a rat model of neonatal white matter damage.

Brehmer, Felix (author)
Bendix, Ivo (author)
Prager, Sebastian (author)
show more...
van de Looij, Yohan (author)
Reinboth, Barbara S (author)
Zimmermanns, Julia (author)
Schlager, Gerald W (author)
Brait, Daniela (author)
Sifringer, Marco (author)
Endesfelder, Stefanie (author)
Sizonenko, Stéphane (author)
Mallard, Carina, 1963 (author)
Gothenburg University,Göteborgs universitet,Institutionen för neurovetenskap och fysiologi, sektionen för fysiologi,Institute of Neuroscience and Physiology, Department of Physiology
Bührer, Christoph (author)
Felderhoff-Mueser, Ursula (author)
Gerstner, Bettina (author)
show less...
 (creator_code:org_t)
2012-11-14
2012
English.
In: PloS one. - : Public Library of Science (PLoS). - 1932-6203. ; 7:11
  • Journal article (peer-reviewed)
Abstract Subject headings
Close  
  • Intrauterine infection and inflammation are major reasons for preterm birth. The switch from placenta-mediated to lung-mediated oxygen supply during birth is associated with a sudden rise of tissue oxygen tension that amounts to relative hyperoxia in preterm infants. Both infection/inflammation and hyperoxia have been shown to be involved in brain injury of preterm infants. Hypothesizing that they might be additive or synergistic, we investigated the influence of a systemic lipopolysaccharide (LPS) application on hyperoxia-induced white matter damage (WMD) in newborn rats. Three-day-old Wistar rat pups received 0.25 mg/kg LPS i.p. and were subjected to 80% oxygen on P6 for 24 h. The extent of WMD was assessed by immunohistochemistry, western blots, and diffusion tensor (DT) magnetic resonance imaging (MRI). In addition, the effects of LPS and hyperoxia were studied in an in vitro co-culture system of primary rat oligodendrocytes and microglia cells. Both noxious stimuli, hyperoxia, and LPS caused hypomyelination as revealed by western blot, immunohistochemistry, and altered WM microstructure on DT-MRI. Even so, cellular changes resulting in hypomyelination seem to be different. While hyperoxia induces cell death, LPS induces oligodendrocyte maturity arrest without cell death as revealed by TUNEL-staining and immunohistological maturation analysis. In the two-hit scenario cell death is reduced compared with hyperoxia treated animals, nevertheless white matter alterations persist. Concordantly with these in vivo findings we demonstrate that LPS pre-incubation reduced premyelinating-oligodendrocyte susceptibility towards hyperoxia in vitro. This protective effect might be caused by upregulation of interleukin-10 and superoxide dismutase expression after LPS stimulation. Reduced expression of transcription factors controlling oligodendrocyte development and maturation further indicates oligodendrocyte maturity arrest. The knowledge about mechanisms that triggered hypomyelination contributes to a better understanding of WMD in premature born infants.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Medicinska och farmaceutiska grundvetenskaper (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Basic Medicine (hsv//eng)

Keyword

Animals
Animals
Newborn
Apoptosis
drug effects
physiology
Brain
drug effects
metabolism
pathology
Caspase 3
metabolism
Cells
Cultured
Hyperoxia
metabolism
pathology
Inflammation
chemically induced
metabolism
pathology
Leukoencephalopathies
metabolism
pathology
Lipopolysaccharides
pharmacology
Microglia
drug effects
metabolism
pathology
Nerve Fibers
Myelinated
drug effects
metabolism
pathology
Oligodendroglia
drug effects
metabolism
pathology
Rats
Rats
Sprague-Dawley
Rats
Wistar

Publication and Content Type

ref (subject category)
art (subject category)

Find in a library

  • PloS one (Search for host publication in LIBRIS)

To the university's database

  • 1 of 1
  • Previous record
  • Next record
  •    To hitlist

Kungliga biblioteket hanterar dina personuppgifter i enlighet med EU:s dataskyddsförordning (2018), GDPR. Läs mer om hur det funkar här.
Så här hanterar KB dina uppgifter vid användning av denna tjänst.

 
pil uppåt Close

Copy and save the link in order to return to this view