Publication: Pharmacological effects of chatuphalatika in hyperuricemia of gout
dc.contributor.author | Vilasinee Hirunpanich Sato | en_US |
dc.contributor.author | Bunleu Sungthong | en_US |
dc.contributor.author | Prasob Orn Rinthong | en_US |
dc.contributor.author | Narawat Nuamnaichati | en_US |
dc.contributor.author | Supachoke Mangmool | en_US |
dc.contributor.author | Savita Chewchida | en_US |
dc.contributor.author | Hitoshi Sato | en_US |
dc.contributor.other | Showa University | en_US |
dc.contributor.other | Mahidol University | en_US |
dc.contributor.other | Mahasarakham University | en_US |
dc.date.accessioned | 2019-08-23T10:40:21Z | |
dc.date.available | 2019-08-23T10:40:21Z | |
dc.date.issued | 2018-01-01 | en_US |
dc.description.abstract | © 2018 The Author(s). Context: Chatuphalatika (CTPT), is a Thai herbal formulation mixture of Phyllanthus emblica Linn. (Euphorbiaceae), Terminalia belerica Linn. (Combretaceae), T. chebula and the fruit of T. arjuna (Roxb.) Wight & Arn. CTPT is considered to exert anti-inflammatory and antihyperuricemic effects, but there have been no reports to demonstrate these pharmacological effects in a quantitative manner. Objectives: To investigate the antioxidative, anti-inflammatory and antihyperuricemic effects of CTPT. Materials and methods: Antioxidant activities of CTPT extracts were measured in vitro by DPPH, ABTS and FRAP assays, and anti-inflammatory effect by measuring inflammatory mediator production induced by lipopolysaccharide (LPS) in RAW264.7 macrophages. The mechanism of the hypouricemic effect was investigated using oxonate-induced hyperuricemic ddY mice treated with oral administrations of CTPT at 250, 500 and 1000 mg/kg. Results: Antioxidant activities of CTPT measured by ABTS and FRAP assays were 1.35 g TEAC/g extract and 10.3mmol/100 g extract, respectively. IC50 for the inhibition of DPPH radical was 13.8 µg/mL. CTPT (10 µg/mL) significantly downregulated the mRNA expression of TNF-α and iNOS in RAW 264.7 cells. Lineweaver-Burk analysis of the enzyme kinetics showed that CTPT inhibited xanthine oxidase (XOD) activity in a noncompetitive manner with the Ki of 576.9 µg/mL. Oral administration of CTPT (1000 mg/kg) significantly suppressed uric acid production by inhibiting hepatic XOD activity, and decreased plasma uric acid levels in hyperuricemic mice by approximately 40% (p<0.05). Conclusions: This study demonstrated for the first time the antioxidative, anti-inflammatory and antihyperuricemic effects of CTPT in vivo and in vitro, suggesting a possibility of using CTPT for the treatment of hyperuricemia in gout. | en_US |
dc.identifier.citation | Pharmaceutical Biology. Vol.56, No.1 (2018), 76-85 | en_US |
dc.identifier.doi | 10.1080/13880209.2017.1421235 | en_US |
dc.identifier.issn | 17445116 | en_US |
dc.identifier.issn | 13880209 | en_US |
dc.identifier.other | 2-s2.0-85046831580 | en_US |
dc.identifier.uri | https://repository.li.mahidol.ac.th/handle/20.500.14594/45310 | |
dc.rights | Mahidol University | en_US |
dc.rights.holder | SCOPUS | en_US |
dc.source.uri | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85046831580&origin=inward | en_US |
dc.subject | Biochemistry, Genetics and Molecular Biology | en_US |
dc.subject | Medicine | en_US |
dc.subject | Pharmacology, Toxicology and Pharmaceutics | en_US |
dc.title | Pharmacological effects of chatuphalatika in hyperuricemia of gout | en_US |
dc.type | Article | en_US |
dspace.entity.type | Publication | |
mu.datasource.scopus | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85046831580&origin=inward | en_US |