Hypothermic Neuronal Rescue from Infection-sensitised Hypoxic-Ischaemic Brain Injury is Pathogen Dependent

Mari Falck, Damjan Osredkar, Elke Maes, Torun Flatebo, Thomas Wood, Hemmen Sabir, Marianne Thoresen

Research output: Contribution to journalArticle (Academic Journal)

15 Citations (Scopus)
257 Downloads (Pure)

Abstract

Perinatal infection increases the vulnerability of the neonatal brain to hypoxic-ischaemic (HI) injury. Hypothermia Treatment (HT) does not provide neuroprotection after pre-insult inflammatory sensitisation by lipopolysaccharide (LPS), a gram-negative bacterial wall constituent. However, early-onset sepsis in term babies is caused by gram-positive species in more than 90 % of cases, and neuro-inflammatory responses triggered through the gram- negative route (toll-like receptor 4; TLR-4), are different from those induced through the gram-positive route via TLR-2. Whether gram-positive septicaemia sensitises the neonatal brain to hypoxia and inhibits the neuroprotective effect of HT is unknown. Seven-day-old (P7) Wistar rats (n=178) were subjected to intraperitoneal injections of PAM3CSK4 (1 mg/kg, a synthetic TLR-2 agonist) or vehicle (0.9% NaCl). After an 8-hour delay, the left carotid artery was ligated followed by 50min of hypoxia (8% O2) at Trectal36°C. Pups received 5h treatment of normothermia (NT, 37°C) or HT (32°C) immediately after the insult. Brains were harvested after seven days’ survival for hemispheric and hippocampal area loss analyses and immunolabelling of microglia (Iba1) and hippocampal neurons (NeuN). Normothermic PAM3CSK4-animals showed significantly more brain injury than vehicle animals (p=0.014). Compared to NT, HT significantly reduced injury in the PAM3CSK4-injected animals, with reduced area loss (p<0.001), reduced microglial activation (p=0.006), and increased neuronal rescue in the CA1 region (p<0.001). Experimental induction of a sepsis-like condition through the gram-positive pathway sensitises the brain to HI. HT was highly neuroprotective after the PAM3CSK4-triggered injury, suggesting HT may be neuroprotective in the presence of a gram-positive infection. These results are in strong contrast to LPS-studies where HT is not neuroprotective.
Original languageEnglish
Pages (from-to)238-247
Number of pages10
JournalDevelopmental Neuroscience
Volume39
Issue number1-4
Early online date14 Apr 2017
DOIs
Publication statusPublished - 2017

Keywords

  • Perinatal brain injury
  • Asphyxia
  • Hypothermia therapy
  • Neuroprotection
  • Infection
  • Inflammation
  • Gram-positive
  • PAM3CSK4
  • LPS

Fingerprint Dive into the research topics of 'Hypothermic Neuronal Rescue from Infection-sensitised Hypoxic-Ischaemic Brain Injury is Pathogen Dependent'. Together they form a unique fingerprint.

  • Cite this