Inhibition of Phosphodiesterase 4 Suppresses Neuronal Ferroptosis After Cerebral Ischemia/Reperfusion

Mol Neurobiol. 2025 Mar;62(3):3376-3395. doi: 10.1007/s12035-024-04495-9. Epub 2024 Sep 17.

Abstract

We have previously shown that inhibition of phosphodiesterase 4 (PDE4) protects against cerebral ischemia/reperfusion injury. However, it remains unclear whether and how PDE4 affects ferroptosis under cerebral ischemia/reperfusion conditions. In this study, we found that overexpression of PDE4B in HT-22 cells exacerbated the detrimental effects of oxygen-glucose deprivation/reoxygenation (OGD/R), including a decrease in cell viability and glutathione (GSH) levels and an increase in Fe2+ content. PDE4B knockdown mitigated the effects of OGD/R, as evidenced by decreased oxidative stress, lactate dehydrogenase (LDH) release, Fe2+ content, and nuclear receptor coactivator 4 (NCOA4) expression. PDE4B knockdown also enhanced the levels of GSH, ferroportin (FPN), and ferritin heavy chain 1 (FTH1). Consistently, inhibition of PDE4 by roflumilast (Roflu) produced similar effects as PDE4B knockdown. Roflu also ameliorated the morphology and membrane potential of the mitochondria. Glutathione peroxidase 4 (GPX4) knockdown blocked the effects of Roflu on cell viability and lipid peroxidation. Moreover, we found that nuclear factor erythroid 2-related factor 2 (Nrf-2) knockdown decreased GPX4 expression. In addition, Nrf-2 knockdown led to enhanced lipid peroxidation, LDH release, and iron levels, while the GSH and FPN levels decreased. More crucially, PDE4 inhibition decreased infarct volume, alleviated oxidative stress, and restored the expression levels of ferroptosis-associated proteins in middle cerebral artery occlusion/reperfusion (MCAO/R) rats. Interestingly, the GPX4 inhibitor RSL3 blocked the neuroprotective effects of Roflu in rats subjected to MCAO/R. Thus, PDE4 inhibition significantly inhibits neuronal ferroptosis by activating the Nrf-2/GPX4 pathway. These data indicate the existence of a novel mechanism underlying the neuroprotective effects of PDE4 inhibition.

Keywords: Cerebral Ischemia; Ferroptosis; Iron; Nrf-2; Oxidative Stress; PDE4.

MeSH terms

  • Aminopyridines / pharmacology
  • Animals
  • Benzamides / pharmacology
  • Brain Ischemia* / drug therapy
  • Brain Ischemia* / metabolism
  • Brain Ischemia* / pathology
  • Carbolines
  • Cell Line
  • Cell Survival / drug effects
  • Cyclic Nucleotide Phosphodiesterases, Type 4* / metabolism
  • Ferroptosis* / drug effects
  • Glucose / deficiency
  • Glutathione / metabolism
  • Male
  • Mice
  • NF-E2-Related Factor 2 / metabolism
  • Neurons* / drug effects
  • Neurons* / metabolism
  • Neurons* / pathology
  • Oxidative Stress / drug effects
  • Phosphodiesterase 4 Inhibitors* / pharmacology
  • Phosphodiesterase 4 Inhibitors* / therapeutic use
  • Phospholipid Hydroperoxide Glutathione Peroxidase / metabolism
  • Rats
  • Rats, Sprague-Dawley
  • Reperfusion Injury* / drug therapy
  • Reperfusion Injury* / enzymology
  • Reperfusion Injury* / metabolism
  • Reperfusion Injury* / pathology

Substances

  • Phosphodiesterase 4 Inhibitors
  • Cyclic Nucleotide Phosphodiesterases, Type 4
  • Phospholipid Hydroperoxide Glutathione Peroxidase
  • NF-E2-Related Factor 2
  • Benzamides
  • Aminopyridines
  • Glutathione
  • Glucose
  • RSL3 compound
  • Carbolines