HIP/PAP prevents excitotoxic neuronal death and promotes plasticity

Parthiv Haldipur, Nina Dupuis, Vincent Degos, Nicolas Moniaux, Vibol Chhor, Sowmyalakshmi Rasika, Leslie Schwendimann, Tifenn le Charpentier, Elodie Rougier, Paul Amouyal, Gilles Amouyal, Pascal Dournaud, Christian Bréchot, Vincent El Ghouzzi, Jamila Faivre, Bobbi Fleiss, Shyamala Mani, Pierre Gressens

Research output: Contribution to journalArticlepeer-review

24 Citations (Scopus)

Abstract

OBJECTIVES: Excitotoxicity plays a significant role in the pathogenesis of perinatal brain injuries. Among the consequences of excessive activation of the N-methyl-d-aspartate (NMDA)-type glutamate are oxidative stress caused by free radical release from damaged mitochondria, neuronal death and subsequent loss of connectivity. Drugs that could protect nervous tissue and support regeneration are attractive therapeutic options. The hepatocarcinoma intestine pancreas protein/pancreatitis-associated protein I (HIP/PAP) or Reg3α, which is approved for clinical testing for the protection and regeneration of the liver, is upregulated in the central nervous system following injury or disease. Here, we examined the neuroprotective/neuroregenerative potential of HIP/PAP following excitotoxic brain injury.

METHODS: We studied the expression of HIP/PAP and two of its putative effectors, cAMP-regulated phosphoprotein 19 (ARPP19) and growth-associated protein 43 (GAP-43), in the neonatal brain, and the protective/regenerative properties of HIP/PAP in three paradigms of perinatal excitotoxicity: intracerebral injection of the NMDA agonist ibotenate in newborn pups, a pediatric model of traumatic brain injury, and cultured primary cortical neurons.

RESULTS: HIP/PAP, ARPP19, and GAP-43 were expressed in the neonatal mouse brain. HIP/PAP prevented the formation of cortical and white matter lesions and reduced neuronal death and glial activation following excitotoxic insults in vivo. In vitro, HIP/PAP promoted neuronal survival, preserved neurite complexity and fasciculation, and protected cell contents from reactive oxygen species (ROS)-induced damage.

INTERPRETATION: HIP/PAP has strong neuroprotective/neuroregenerative potential following excitotoxic injury to the developing brain, and could represent an interesting therapeutic strategy in perinatal brain injury.

Original languageEnglish
Pages (from-to)739-754
Number of pages16
JournalAnnals of Clinical and Translational Neurology
Volume1
Issue number10
DOIs
Publication statusPublished - Oct 2014

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