Research Progress of Natural Active Substances with Uric-Acid-Reducing Activity

J Agric Food Chem. 2022 Dec 21;70(50):15647-15664. doi: 10.1021/acs.jafc.2c06554. Epub 2022 Dec 8.

Abstract

Hyperuricemia is a metabolic disease caused by the accumulation of uric acid in the body. Allopurinol, benzbromarone, and febuxostat, which are available in the market, have reduced the circulating urate levels; however, they exhibit serious side effects. Therefore, it is reasonable to develop a new active antihyperuricemia drug with few side effects. With the deepening of research, numerous kinds of literature have shown that natural active substances are effective in the treatment of hyperuricemia with a variety of sources and few side effects, which have become the focus of research in recent years. This review focuses on natural active substances with uric-acid-reducing activity and discusses their pharmacological effects. More specifically, the bioactive compounds of natural active substances are divided into five categories: natural extracts, monomer compounds extracted from plants, natural protease hydrolysates, peptides, and probiotic bacteria. In addition, the mechanisms by which these bioactive compounds exhibit hypouricemic effects can be divided into four classes: inhibition of key enzyme activities, promotion of uric acid excretion and inhibition of reabsorption in the kidney, promotion of decomposing uric acid precursors, and promotion of decomposing uric acid. Overall, this current and comprehensive review examines the role of natural active substances in the treatment of hyperuricemia.

Keywords: adenosine deaminase; hyperuricemia; natural active substance; xanthine oxidase.

Publication types

  • Review

MeSH terms

  • Allopurinol
  • Febuxostat / metabolism
  • Febuxostat / pharmacology
  • Febuxostat / therapeutic use
  • Humans
  • Hyperuricemia* / drug therapy
  • Hyperuricemia* / metabolism
  • Kidney / metabolism
  • Uric Acid / metabolism
  • Xanthine Oxidase / metabolism

Substances

  • Uric Acid
  • Febuxostat
  • Allopurinol
  • Xanthine Oxidase