AI Article Synopsis

  • Preterm birth can lead to brain injuries and long-term behavioral issues due to the loss of neurosteroid support from the placenta, increasing the risk of excitotoxic damage.
  • The study used guinea pigs to test zuranolone, an analogue of allopregnanolone, by administering it to preterm pups and analyzing behavior and brain structure.
  • Zuranolone treatment improved behavioral outcomes, prevented hyperactivity in male pups, and restored myelination and neurotransmitter pathways in preterm offspring, suggesting its potential as a neuroprotective therapy for preventing long-term impairments after preterm birth.

Article Abstract

Background: Preterm birth is associated with brain injury and long-term behavioral abnormalities, for which there are limited prevention options. When born preterm, infants prematurely lose placental neurosteroid (allopregnanolone) support. This increases the risk of excitotoxic damage to the brain, which increases the risk of injury, causing long-term deficits in behavior, myelination, and alterations to neurotransmitter pathways. We propose that postnatal restoration of neurosteroid action through zuranolone therapy will reduce neurological impairments following preterm birth.

Methods: Guinea pig dams underwent survival cesarean section surgery to deliver pups prematurely (GA64) or at term (GA69). Between birth and term equivalence age, preterm pups received vehicle (15% β-cyclodextrin) or the allopregnanolone analogue zuranolone (1 mg/kg/day). Behavioral analysis was performed at postnatal day (PND) 7 and 40, before tissue collection at PND 42. Immunostaining for myelin basic protein (MBP), as well as real-time polymerase chain reaction to characterize oligodendrocyte lineage and neurotransmitter pathways, was performed in frontal cortex tissues.

Results: Zuranolone treatment prevented the hyperactive phenotype in preterm-born offspring, most markedly in males. Additionally, preterm-related reductions in MBP were ameliorated. Several preterm-related alterations in mRNA expression of dopaminergic, glutamatergic, and GABAergic pathways were also restored back to that of a term control level.

Conclusion: This is the first study to assess zuranolone treatment as a neuroprotective therapy following preterm birth. Zuranolone treatment improved behavioral outcomes and structural changes in the preterm offspring, which continued long term until at least a late childhood timepoint. Clinical studies are warranted for further exploring the neuroprotective possibilities of this treatment following preterm birth.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11376442PMC
http://dx.doi.org/10.1002/brb3.70009DOI Listing

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