Eggshell Membrane Ameliorates Hyperuricemia by Increasing Urate Excretion in Potassium Oxonate-Injected Rats

• Published in: Nutrients 2021-09, Vol.13 (10), p.3323
• Main Authors: Sung, Yoon-Young, Kim, Dong-Seon
• Format: Article
• Language: English
• Subjects: Animals; Arthritis; ATP-binding cassette transporter G2; Biomedical materials; Creatinine; Egg Shell - physiology; Egg shells; Eggs; Enzymes; Excretion; Gametocytes; Glucose transporter; Gout; Histopathology; Humans; Hyperuricemia; Hyperuricemia - blood; Hyperuricemia - physiopathology; Hyperuricemia - urine; IL-1β; Inflammation - pathology; Inflammation - physiopathology; Injections; Kidney - pathology; Kidney - physiopathology; Kidney Function Tests; Liver; Male; Membranes; Metabolic disorders; Oocytes; Oocytes - metabolism; Organic Anion Transporters - metabolism; Osteoarthritis; Oxonic Acid - administration & dosage; Pain; Potassium; potassium oxonate; Proteins; Rats; Rats, Sprague-Dawley; Renal function; Rheumatism; Sodium; Stiffness; urate transporter 1; Urea; Uric acid; Uric Acid - blood; Uric Acid - urine; Urine; Xanthine oxidase; Xanthine Oxidase - metabolism; Xenopus
• ISSN: 2072-6643; 2072-6643
• DOI: 10.3390/nu13103323

Hyperuricemia is the primary cause of gouty arthritis and other metabolic disorders. Eggshell membrane (EM) is an effective and safe supplement for curing pain and stiffness connected with osteoarthritis. However, the effect of EM on hyperuricemia is unclear. This study determines the effects of EM on potassium oxonate-injected hyperuricemia. Uric acid, creatinine, blood urea nitrogen concentrations in the serum, and xanthine oxidase activity in the liver are measured. Protein levels of renal urate transporter 1 (URAT1), organic anion transporters 1 (OAT1), glucose transporter 9 (GLUT9), and ATP-binding cassette transporter G2 (ABCG2) in the kidney are determined with renal histopathology. The results demonstrate that EM reduces serum uric acid levels and increases urine uric acid levels in hyperuricemic rats. Moreover, EM downregulates renal URAT1 protein expression, upregulates OAT1 and ABCG2, but does not change GLUT9 expression. Additionally, EM does not change xanthine oxidase activity in the liver or the serum. EM also decreases uric acid uptake into oocytes expressing hURAT1. Finally, EM markedly reduces renal inflammation and serum interleukin-1β levels. These findings suggest that EM exhibits antihyperuricemic effects by promoting renal urate excretion and regulating renal urate transporters. Therefore, EM may be useful in the prevention and treatment of gout and hyperuricemia.