Cpd-A1 alleviates acute kidney injury by inhibiting ferroptosis

Acta Pharmacol Sin. 2024 Aug;45(8):1673-1685. doi: 10.1038/s41401-024-01277-w. Epub 2024 Apr 19.

Abstract

Acute kidney injury (AKI) is defined as sudden loss of renal function characterized by increased serum creatinine levels and reduced urinary output with a duration of 7 days. Ferroptosis, an iron-dependent regulated necrotic pathway, has been implicated in the progression of AKI, while ferrostatin-1 (Fer-1), a selective inhibitor of ferroptosis, inhibited renal damage, oxidative stress and tubular cell death in AKI mouse models. However, the clinical translation of Fer-1 is limited due to its lack of efficacy and metabolic instability. In this study we designed and synthesized four Fer-1 analogs (Cpd-A1, Cpd-B1, Cpd-B2, Cpd-B3) with superior plasma stability, and evaluated their therapeutic potential in the treatment of AKI. Compared with Fer-1, all the four analogs displayed a higher distribution in mouse renal tissue in a pharmacokinetic assay and a more effective ferroptosis inhibition in erastin-treated mouse tubular epithelial cells (mTECs) with Cpd-A1 (N-methyl-substituted-tetrazole-Fer-1 analog) being the most efficacious one. In hypoxia/reoxygenation (H/R)- or LPS-treated mTECs, treatment with Cpd-A1 (0.25 μM) effectively attenuated cell damage, reduced inflammatory responses, and inhibited ferroptosis. In ischemia/reperfusion (I/R)- or cecal ligation and puncture (CLP)-induced AKI mouse models, pre-injection of Cpd-A1 (1.25, 2.5, 5 mg·kg-1·d-1, i.p.) dose-dependently improved kidney function, mitigated renal tubular injury, and abrogated inflammation. We conclude that Cpd-A1 may serve as a promising therapeutic agent for the treatment of AKI.

Keywords: AKI; Cpd-A1; ferroptosis; ferrostatin-1; lipid peroxidation; tissue distribution.

MeSH terms

  • Acute Kidney Injury* / drug therapy
  • Acute Kidney Injury* / metabolism
  • Animals
  • Cyclohexylamines / pharmacology
  • Cyclohexylamines / therapeutic use
  • Epithelial Cells / drug effects
  • Epithelial Cells / metabolism
  • Ferroptosis* / drug effects
  • Male
  • Mice
  • Mice, Inbred C57BL*
  • Phenylenediamines* / pharmacology
  • Phenylenediamines* / therapeutic use
  • Reperfusion Injury / drug therapy
  • Reperfusion Injury / metabolism

Substances

  • Phenylenediamines
  • ferrostatin-1
  • Cyclohexylamines