Study on the Anti-Gout Activity of Chlorogenic Acid: Improvement on Hyperuricemia and Gouty Inflammation

被引:63
|
作者
Meng, Zhao-Qing [1 ,2 ]
Tang, Zhao-Hui [2 ]
Yan, Yun-Xia [1 ]
Guo, Chang-Run [1 ]
Cao, Liang [2 ]
Ding, Gang [2 ]
Huang, Wen-Zhe [2 ]
Wang, Zhen-Zhong [2 ]
Wang, Kelvin D. G. [1 ]
Xiao, Wei [2 ]
Yang, Zhong-Lin [1 ]
机构
[1] China Pharmaceut Univ, State Key Lab Nat Med, Nanjing 210009, Jiangsu, Peoples R China
[2] Jiangsu Kanion Pharmaceut Co Ltd, Lianyungang 222001, Jiangsu, Peoples R China
来源
AMERICAN JOURNAL OF CHINESE MEDICINE | 2014年 / 42卷 / 06期
关键词
Chlorogenic acid; Hyperuricemia; Gouty Arthritis; Xanthine Oxidase; Monosodium; Urate Crystals; Interleukin-1; beta; HYPOURICEMIC ACTION; INHIBITORY-ACTIVITY; DUAL ACTIONS; MICE; ARTHRITIS; EXTRACT; TRANSPORTERS; ATTENUATION; RATS;
D O I
10.1142/S0192415X1450092X
中图分类号
R [医药、卫生];
学科分类号
10 ;
摘要
Gout is a metabolic disorder associated with hyperuricemia resulting in the deposition of monosodium urate (MSU) crystals in joints and tissues. Lowering serum uric acid (Sur) levels and anti-inflammation are highly essential in treating gout. Chlorogenic acid (CA), as one of the most abundant polyphenols in the Chinese medicines, has been rarely reported to have an anti-gout effect. The model of potassium oxonate (PO)-induced hyperuricemia in mice and MSU crystal-induced inflammation in rats has been established in this study. The potential beneficial effects and mechanisms of CA on hyperuricemia and gouty arthritis were elucidated. The results demonstrated that CA significantly decreased the Sur level by inhibiting the xanthine oxidase (XOD) activity but not increasing the urinary uric acid (Uur) level. In addition, CA also exhibited the effect of suppressing paw swelling. Further investigation indicated that CA improved the symptoms of inflammation induced by MSU crystals by inhibiting the production of proinflammatory cytokines including interleukin-1 beta (IL-1 beta), interleukin-6 (IL-6), and tumor necrosis factor-alpha (TNF-alpha). The present study suggests that CA may have a considerable potential for development as an anti-gouty arthritis agent for clinical application.
引用
收藏
页码:1471 / 1483
页数:13
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