LAUSR.org creates dashboard-style pages of related content for over 1.5 million academic articles. Sign Up to like articles & get recommendations!

In-Silico and in-Vitro Evaluation of Xanthine Oxidase Inhibition of Zingiber officinalae for Hypouricemic activity

Photo by robbie36 from unsplash

Zingiber officinale (ZO), traditionally known for its remedial potential, was examined on phytoconstituents analysis, antioxidant and xanthine oxidase inhibition by in-vitro analysis, followed by an in-silico study to identify the… Click to show full abstract

Zingiber officinale (ZO), traditionally known for its remedial potential, was examined on phytoconstituents analysis, antioxidant and xanthine oxidase inhibition by in-vitro analysis, followed by an in-silico study to identify the biological rationale. Results show that ethanolic extract of Zingiber officinale illustrated potential antioxidant to that of standard. DPPH ZO (IC50=42.09ug/mL), DPPH butylhydroxyltoluene (IC50=66.67ug/mL), nitric oxide ZO (IC50=28.36ug/mL), nitric oxide ascorbic acid (IC50=42.87??g/mL). Zingiber officinale extract inhibited the xanthine oxidase activity (IC50 = 188.5ug/mL) compared to allopurinol (IC50=499.2ug/mL), which showed competitive inhibition. The in-silico docking studies of the major phytoconstituents revealed by GC-MS analysis from this extract suggest that the inhibitory activity may be due to the combined effect of these compounds. These results suggest substantial reason for the evaluation of active compounds in in-vivo system for the management and treatment of gout as well as in the oxidative stress conditions.

Keywords: xanthine oxidase; zingiber; activity; oxidase inhibition

Journal Title: Research Journal of Pharmacy and Technology
Year Published: 2019

Link to full text (if available)


Share on Social Media:                               Sign Up to like & get
recommendations!

Related content

More Information              News              Social Media              Video              Recommended



                Click one of the above tabs to view related content.