Lycium barbarum polysaccharides protect mice from hyperuricaemia through promoting kidney excretion of uric acid and inhibiting liver xanthine oxidase

Pharm Biol. 2020 Dec;58(1):944-949. doi: 10.1080/13880209.2020.1817951.

Abstract

Context: Lycium barbarum L. (Solanaceae) polysaccharides (LBPs) are important active constituents that have demonstrated kidney protection.

Objective: This study investigated the effect of LBPs on hyperuricaemia and explored the underlying mechanism in mice.

Materials and methods: Thirty-six C57BL/6 mice were randomly divided into the control group, hyperuricaemia group, allopurinol group (5 mg/kg) and three LBP groups (n = 6). The LBP groups were treated orally with LBPs at 50, 100 and 200 mg/kg body weight for 7 days. We examined the levels of serum uric acid (SUA) and urinary uric acid (UUA), as well as xanthine oxidase (XOD) activities. mRNA and protein were quantified by quantitative real-time PCR and Western blotting, respectively.

Results: LBPs treatment (100 and 200 mg/kg) significantly reduced the SUA levels to 4.83 and 4.48 mg/dL, and markedly elevated the UUA levels to 4.68 and 5.18 mg/dL (p < 0.05), respectively, while significantly increased the mRNA and protein expression levels of renal organic anti-transporter 1 (OAT1) and organic anti-transporter 3 (OAT3), and markedly decreased the levels of glucose transporter 9 (GLUT9) (p < 0.05). Additionally, the serum XOD activities were reduced to 31.5 and 31.1 mU/mL, and the liver XOD activities were reduced to 80.6 and 75.6 mU/mL after treatment with 100 and 200 mg/kg LBPs (p < 0.01), respectively.

Discussion and conclusions: This study demonstrated the potential role of LBPs in reducing the uric acid level in hyperuricemic mice. A border study population should be evaluated. These results are valuable for the development of new anti-hyperuricaemia agents from LBPs.

Keywords: Organic anti-transporter 1; glucose transporter 9; organic anti-transporter 3.

MeSH terms

  • Animals
  • Drugs, Chinese Herbal / pharmacology*
  • Glucose Transport Proteins, Facilitative / metabolism
  • Hyperuricemia / drug therapy*
  • Hyperuricemia / prevention & control
  • Kidney / drug effects
  • Liver / drug effects
  • Lycium / chemistry
  • Male
  • Medicine, Chinese Traditional
  • Mice
  • Mice, Inbred C57BL
  • Organic Anion Transport Protein 1 / metabolism
  • Organic Anion Transporters, Sodium-Independent / metabolism
  • Protective Agents / pharmacology*
  • Uric Acid / blood
  • Uric Acid / metabolism*
  • Xanthine Oxidase / blood
  • Xanthine Oxidase / metabolism*

Substances

  • Drugs, Chinese Herbal
  • Glucose Transport Proteins, Facilitative
  • Organic Anion Transport Protein 1
  • Organic Anion Transporters, Sodium-Independent
  • Protective Agents
  • Slc22a6 protein, mouse
  • Slc2a9 protein, mouse
  • lycium barbarum polysaccharide
  • organic anion transport protein 3
  • Uric Acid
  • Xanthine Oxidase

Grants and funding

This article was supported by the Natural Science Foundation of Liaoning Province [2020-BS-284].