Mesoporous zinc-polyphenol nanozyme for attenuating renal ischemia-reperfusion injury

Nanomedicine (Lond). 2024;19(24):2011-2026. doi: 10.1080/17435889.2024.2382667. Epub 2024 Aug 8.

Abstract

Aim: To target the reactive oxygen species (ROS) accumulation and renal tubular epithelial cell (rTEC) death in renal ischemia-reperfusion injury (IRI), we constructed a nanoparticle that offers ROS scavenging and rTEC-death inhibition: mesoporous zinc-tannic acid nanozyme (ZnTA).Materials & methods: After successfully constructing ZnTA, we proceeded to examine its effect on ROS accumulation, cellular ferroptosis and apoptosis, as well as injury severity.Results: Malondialdehyde, Fe2+ amounts and 4-HNE staining demonstrated that ZnTA effectively attenuated rTEC ferroptosis. TUNEL staining confirmed that Zn2+ carried by ZnTA could effectively inhibit caspase 3 and caspase 9, mitigating apoptosis. Finally, it reduced renal IRI through the synergistic effect of ROS scavenging and cell-death inhibition.Conclusion: This study is expected to provide a paradigm for a combined therapeutic strategy for renal IRI.

Keywords: ROS scavenging; ferroptosis; mesoporous nanoparticles; metal–polyphenol hybrids; renal ischemia–reperfusion injury.

Plain language summary

[Box: see text].

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis / drug effects
  • Cell Line
  • Epithelial Cells / drug effects
  • Epithelial Cells / metabolism
  • Ferroptosis* / drug effects
  • Humans
  • Kidney / drug effects
  • Kidney / metabolism
  • Kidney / pathology
  • Kidney Tubules / drug effects
  • Kidney Tubules / metabolism
  • Kidney Tubules / pathology
  • Male
  • Mice
  • Nanoparticles / chemistry
  • Porosity
  • Reactive Oxygen Species* / metabolism
  • Reperfusion Injury* / drug therapy
  • Reperfusion Injury* / metabolism
  • Zinc* / chemistry
  • Zinc* / pharmacology

Substances

  • Reactive Oxygen Species
  • Zinc