URB447 Is Neuroprotective in Both Male and Female Rats after Neonatal Hypoxia-Ischemia and Enhances Neurogenesis in Females

Int J Mol Sci. 2024 Jan 28;25(3):1607. doi: 10.3390/ijms25031607.

Abstract

The need for new and effective treatments for neonates suffering from hypoxia-ischemia is urgent, as the only implemented therapy in clinics is therapeutic hypothermia, only effective in 50% of cases. Cannabinoids may modulate neuronal development and brain plasticity, but further investigation is needed to better describe their implication as a neurorestorative therapy after neonatal HI. The cannabinoid URB447, a CB1 antagonist/CB2 agonist, has previously been shown to reduce brain injury after HI, but it is not clear whether sex may affect its neuroprotective and/or neurorestorative effect. Here, URB447 strongly reduced brain infarct, improved neuropathological score, and augmented proliferative capacity and neurogenic response in the damaged hemisphere. When analyzing these effects by sex, URB447 ameliorated brain damage in both males and females, and enhanced cell proliferation and the number of neuroblasts only in females, thus suggesting a neuroprotective effect in males and a double neuroprotective/neurorestorative effect in females.

Keywords: endocannabinoid system; neonatal hypoxia–ischemia; neurogenesis; neuroprotection.

MeSH terms

  • Animals
  • Animals, Newborn
  • Benzyl Compounds*
  • Brain / pathology
  • Brain Injuries* / pathology
  • Cannabinoids* / pharmacology
  • Female
  • Hypoxia-Ischemia, Brain* / pathology
  • Ischemia / pathology
  • Male
  • Neurogenesis
  • Neuroprotective Agents* / pharmacology
  • Neuroprotective Agents* / therapeutic use
  • Pyrroles*
  • Rats
  • Rats, Wistar

Substances

  • (4-amino-1-(4-chlorobenzyl)-2-methyl-5-phenyl-1H-pyrrol-3-yl)(phenyl)methanone
  • Neuroprotective Agents
  • Cannabinoids
  • Benzyl Compounds
  • Pyrroles