Self-Cascade Uricase/Catalase Mimics Alleviate Acute Gout

Nano Lett. 2022 Jan 12;22(1):508-516. doi: 10.1021/acs.nanolett.1c04454. Epub 2021 Dec 30.

Abstract

Uricase-based therapies are limited for gout partially due to the accumulation of H2O2 in an arthrosis environment with slow metabolism. To tackle this limitation, previous studies adopted a cascade reaction between the degradation of uric acid (UA) and timely elimination of H2O2 using complicated composites of uricase and catalase (CAT)/CAT-like nanozyme. Herein, the self-cascade nanozyme Pt/CeO2 with high efficiency toward simultaneous UA degradation and H2O2 elimination is demonstrated on the basis of both uricase- and CAT-like activities in Pt, Ir, Rh, and Pd platinum-group metals. With an optimized molar ratio of Pt and CeO2, Pt/CeO2 (1/5) not only does better in degrading UA but also has excellent reactive oxygen species (ROS) and reactive nitrogen species (RNS) scavenging activities. In monosodium urate (MSU)-induced acute gout rats, Pt/CeO2 nanozyme markedly alleviates pain along with joint edema, thus improving gait claudication and tissue inflammation. These results provide novel insights into strategies of an efficient enzyme-mimetic treatment for gout.

Keywords: Acute gout; H2O2 elimination; Platinum-group metal; Self-cascade nanozyme; Uric acid degradation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Catalase* / therapeutic use
  • Enzyme Therapy*
  • Gout* / drug therapy
  • Hydrogen Peroxide / metabolism
  • Rats
  • Urate Oxidase* / therapeutic use
  • Uric Acid / metabolism

Substances

  • Uric Acid
  • Hydrogen Peroxide
  • Catalase
  • Urate Oxidase