Comparing the Effects of Febuxostat and Allopurinol in an Animal Model of Metabolic Syndrome

Pharmacology. 2021;106(9-10):564-572. doi: 10.1159/000516495. Epub 2021 Jun 28.

Abstract

Introduction: Recent studies highlighted the association of hyperuricemia and metabolic syndrome (MS). The aim of this study was to compare the beneficial effects of febuxostat versus allopurinol on the biochemical changes that occur in MS.

Methods: Forty adult male Sprague Dawley albino rats were used in the study. Insulin resistance and MS were induced by administration of a high-fructose diet for 8 weeks. Follow-up of changes in weight, blood pressure, serum biochemical parameters, serum antioxidant catalase, and glutathione peroxidase activities was done. At the end of the study, animals were sacrificed, and the thoracic aorta was isolated for in vitro study of the endothelial integrity.

Results: Allopurinol and febuxostat treatment induced significant reduction in body weight, systolic blood pressure, blood glucose, insulin, lipids, and improved kidney functions and endothelial integrity compared to nontreated rats. Febuxostat was more effective than allopurinol in normalizing serum fasting glucose, uric acid, catalase, and glutathione peroxidase activities.

Conclusion: Xanthine oxidase inhibitors ameliorated the effects of MS. Febuxostat was mildly superior to allopurinol in lowering serum fasting glucose, lipids, uric acid, and antioxidant enzyme activities.

Keywords: Allopurinol; Febuxostat; Metabolic syndrome; Urate-lowering therapy.

MeSH terms

  • Allopurinol / pharmacology*
  • Animals
  • Blood Glucose / drug effects
  • Blood Pressure / drug effects
  • Body Weight / drug effects
  • Catalase / drug effects
  • Disease Models, Animal
  • Febuxostat / pharmacology*
  • Glutathione Peroxidase / drug effects
  • Insulin Resistance
  • Male
  • Metabolic Syndrome / drug therapy*
  • Rats
  • Rats, Sprague-Dawley
  • Xanthine Oxidase / antagonists & inhibitors*

Substances

  • Blood Glucose
  • Febuxostat
  • Allopurinol
  • Catalase
  • Glutathione Peroxidase
  • Xanthine Oxidase