| Literature DB >> 28521370 |
Jin Kyu Kim1, Woo Jung Kim1, Jung Mi Hyun1, Jong Suk Lee1, Jin Gwan Kwon1, Changon Seo1, Myung-Jin Song1, Chun Whan Choi1, Seong Su Hong1, Kyuhee Park1, Pansoo Kim1, Hachang Sung2, Jin Koo Lee3, Yongmun Choi1.
Abstract
Hyperuricemia is a clinical condition characterized by an elevated level of serum uric acid and is a key risk factor for the development of gout and metabolic disorders. The existing urate-lowering therapies are often impractical for certain patient populations, providing a rationale to explore new agents with improved safety and efficacy. Here, we discovered that Salvia plebeia extract inhibited the enzyme activity of xanthine oxidase, which is a key enzyme generating uric acid in the liver. In an animal model of hyperuricemia, S. plebeia extract reduced serum urate to the levels observed in control animals. The urate-lowering effect of S. plebeia extract in vivo was supported by the identification of compounds that inhibit xanthine oxidase enzyme activity in vitro. Nepetin, scutellarein, and luteolin contributed significantly to S. plebeia bioactivity in vitro. These compounds showed the highest potency against xanthine oxidase with IC50 values of 2.35, 1.74, and 1.90 µM, respectively, and were present at moderate quantities. These observations serve as a basis for further elaboration of the S. plebeia extracts for the development of new therapeutics for hyperuricemia and related diseases. Georg Thieme Verlag KG Stuttgart · New York.Entities:
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Year: 2017 PMID: 28521370 DOI: 10.1055/s-0043-111012
Source DB: PubMed Journal: Planta Med ISSN: 0032-0943 Impact factor: 3.352