Inhibition of xanthine oxidase activity by gnaphalium affine extract.
- Author:
Wei-qing LIN
1
,
2
;
Jian-xiang XIE
3
;
Xiao-mu WU
4
;
Lin YANG
4
;
Hai-dong WANG
1
;
Author Information
- Publication Type:Journal Article
- MeSH: Flavonoids; pharmacology; Gnaphalium; chemistry; Xanthine Oxidase; antagonists & inhibitors
- From: Chinese Medical Sciences Journal 2014;29(4):225-230
- CountryChina
- Language:English
-
Abstract:
OBJECTIVETo evaluate the inhibitory effect of Gnaphalium affine extracts on xanthine oxidase (XO) activity in vitro and to analyze the mechanism of this effect.
METHODSIn this in vitro study, Kinetic measurements were performed in 4 different inhibitor concentrations and 5 different xanthine concentrations (60, 100, 200, 300, 400 Μmol/L). Dixon and Lineweaver-Burk plot analysis were used to determine Ki values and the inhibition mode for the compounds isolated from Gnaphalium affine extract.
RESULTSFour potent xanthine oxidase inhibitors were found in 95% ethanolic (v/v) Gnaphalium affine extract. Among them, the flavone Eupatilin exhibited the strongest inhibitory effect on XO with a inhibition constant (Ki) of 0.37 Μmol/L, lower than the Ki of allopurinol (4.56 mol/L), a known synthetic XO inhibitor. Apigenin (Ki of 0.56 Μmol/L, a proportion of 0.0053‰ in Gnaphalium affine), luteolin (Ki of 2.63 Μmol/L, 0.0032‰ in Gnaphalium affine) and 5-hydroxy-6,7,3',4'-tetramethoxyflavone (Ki of 3.15 Μmol/L, 0.0043‰ in Gnaphalium affine) also contributed to the inhibitory effect of Gnaphalium affine extract on XO activity.
CONCLUSIONSThese results suggest that the use of Gnaphalium affine in the treatment of gout could be attributed to its inhibitory effect on XO. This study provides a rational basis for the traditional use of Gnaphalium affine against gout.