Melatonin reduces brain injury following inflammation-amplified hypoxia-ischemia in a translational newborn piglet study of neonatal encephalopathy

Raymand Pang; Christopher Meehan; George Maple; Georgina Norris; Ellie Campbell; Katie Tucker; Alison Mintoft; Francisco Torrealdea; Alan Bainbridge; Mariya Hristova; John Barks; Xavier Golay; Joseph Standing; Nicola J Robertson

doi:10.1111/jpi.12962

Melatonin reduces brain injury following inflammation-amplified hypoxia-ischemia in a translational newborn piglet study of neonatal encephalopathy

J Pineal Res. 2024 May;76(4):e12962. doi: 10.1111/jpi.12962.

Authors

Affiliations

¹ Institute for Women's Health, University College London, London, UK.
² Medical Physics and Biomedical Engineering, University College London Hospitals, London, UK.
³ Department of Paediatrics, University of Michigan Medical School, Ann Arbor, Michigan, USA.
⁴ Institute of Neurology, Queen's Square, University College London, London, UK.
⁵ Great Ormond Street Institute of Child Health, University College London, London, UK.
⁶ Centre for Clinical Brain Sciences, University of Edinburgh, Edinburgh, UK.

PMID: 38775315
DOI: 10.1111/jpi.12962

Abstract

There is a need to develop therapies for neonatal encephalopathy (NE) in low- and middle-income countries (LMICs) where the burden of disease is greatest and therapeutic hypothermia (HT) is not effective. We aimed to assess the efficacy of melatonin following inflammation-amplified hypoxia-ischaemia (IA-HI) in the newborn piglet. The IA-HI model accounts for the contribution of infection/inflammation in this setting and HT is not cytoprotective. We hypothesised that intravenous melatonin (5% ethanol, at 20 mg/kg over 2 h at 1 h after HI + 10 mg/kg/12 h between 24 and 60 h) is safe and associated with: (i) reduction in magnetic resonance spectroscopy lactate/N-acetylaspartate (MRS Lac/sNAA); (ii) preservation of phosphorus MRS phosphocreatine/phosphate exchange pool (PCr/Epp); (iii) improved aEEG/EEG recovery and (iv) cytoprotection on immunohistochemistry. Male and female piglets underwent IA-HI by carotid artery occlusion and reduction in FiO₂ to 6% at 4 h into Escherichia coli lipopolysaccharide sensitisation (2 μg/kg bolus + 1 μg/kg/h over 12 h). At 1 h after IA-HI, piglets were randomised to HI-saline (n = 12) or melatonin (n = 11). There were no differences in insult severity between groups. Target melatonin levels (15-30 mg/L) were achieved within 3 h and blood ethanol levels were <0.25 g/L. At 60 h, compared to HI-saline, melatonin was associated with a reduction of 0.197 log₁₀ units (95% CrI [-0.366, -0.028], Pr_(sup) 98.8%) in basal-ganglia and thalamic Lac/NAA, and 0.257 (95% CrI [-0.676, 0.164], Pr_(sup) 89.3%) in white matter Lac/NAA. PCr/Epp was higher in melatonin versus HI-saline (Pr_(sup) 97.6%). Melatonin was associated with earlier aEEG/EEG recovery from 19 to 24 h (Pr_(sup) 95.4%). Compared to HI-saline, melatonin was associated with increased NeuN+ cell density (Pr_(sup) 99.3%) across five of eight regions and reduction in TUNEL-positive cell death (Pr_(sup) 89.7%). This study supports the translation of melatonin to early-phase clinical trials. Melatonin is protective following IA-HI where HT is not effective. These data guide the design of future dose-escalation studies in the next phase of the translational pipeline.

Keywords: hypoxia–ischaemia; inflammation; melatonin; neonatal encephalopathy; neuroprotection.

MeSH terms

Animals
Animals, Newborn*
Disease Models, Animal
Female
Hypoxia-Ischemia, Brain* / drug therapy
Hypoxia-Ischemia, Brain* / metabolism
Inflammation / drug therapy
Inflammation / metabolism
Male
Melatonin* / pharmacology
Swine

Abstract

MeSH terms

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