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Journal of Biological Sciences
  Year: 2018 | Volume: 18 | Issue: 8 | Page No.: 468-474
DOI: 10.3923/jbs.2018.468.474
Anti-hyperuricemic, Uricosuric and Xanthine-oxidase Inhibitory Activities of Watermelon Powder in a Rat Gout Model
Basim Jasim Hameed , Falah Hassan Shari and Usama Hamid Ramadhan

Abstract:
Background and Objective: Gout is a common metabolic disorder around the world. It characterized by elevation of uric acid levels in the blood, leading to increase the deposition of urate crystals in the joints and kidneys. The current study was carried out to investigate the efficacy and mechanism action of watermelon powder as antihyperuricemic agent. Materials and Methods: Enzyme assay was done by using bovine milk xanthine oxidase (XO). The XO inhibitory activity in vitro was performed by using different doses of watermelon powder and the degree of XO inhibition was expressed as IC50. The antihyperuricemic and uricosuric activity of watermelon were tested in the potassium oxonate-induced hyperuricemic rats for seven consecutive days of oral treatment of 25, 50 and 100 mg kg–1 doses. Results: The results of the study revealed that the watermelon has a moderate activity of XO inhibition with IC50 =95.24 μg mL–1. In addition, these results showed that all doses of watermelon powder were able to significant reduce serum uric acid levels in the hyperuricemic rats. Moreover, the results of uricosuric activity assay showed that the watermelon significantly increased the urinary excretion of uric acid. Conclusion: The watermelon powder showed significant effects on the evaluated models and therefore it may be promising agent for the treatment of gout since it possesses a moderate xanthine oxidase inhibitory and a potent of both antihyperuricemic and uricosuric effects.
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How to cite this article:

Basim Jasim Hameed, Falah Hassan Shari and Usama Hamid Ramadhan, 2018. Anti-hyperuricemic, Uricosuric and Xanthine-oxidase Inhibitory Activities of Watermelon Powder in a Rat Gout Model. Journal of Biological Sciences, 18: 468-474.

DOI: 10.3923/jbs.2018.468.474

URL: https://scialert.net/abstract/?doi=jbs.2018.468.474

 
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