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姜黄素抗炎作用的机制:PPAR-γ 激活。

Mechanism of the Anti-inflammatory Effect of Curcumin: PPAR-gamma Activation.

机构信息

Division of Surgical Research, North Shore University Hospital and Long Island Jewish Medical Center, 350 Community Drive, Manhasset, NY 11030, USA.

出版信息

PPAR Res. 2007;2007:89369. doi: 10.1155/2007/89369.

Abstract

Curcumin, the phytochemical component in turmeric, is used as a dietary spice and a topical ointment for the treatment of inflammation in India for centuries. Curcumin (diferuloylmethane) is relatively insoluble in water, but dissolves in acetone, dimethylsulphoxide, and ethanol. Commercial grade curcumin contains 10-20% curcuminoids, desmethoxycurcumin, and bisdesmethoxycurcumin and they are as effective as pure curcumin. Based on a number of clinical studies in carcinogenesis, a daily oral dose of 3.6 g curcumin has been efficacious for colorectal cancer and advocates its advancement into Phase II clinical studies. In addition to the anticancer effects, curcumin has been effective against a variety of disease conditions in both in vitro and in vivo preclinical studies. The present review highlights the importance of curcumin as an anti-inflammatory agent and suggests that the beneficial effect of curcumin is mediated by the upregulation of peroxisome proliferator-activated receptor-gamma (PPAR-gamma) activation.

摘要

姜黄素是姜黄中的植物化学成分,在印度,几个世纪以来,它一直被用作膳食香料和局部软膏,用于治疗炎症。姜黄素(二芳基甲烷)在水中的溶解度相对较低,但可溶于丙酮、二甲基亚砜和乙醇。商业级姜黄素含有 10-20%的姜黄素类、脱甲氧基姜黄素和双脱甲氧基姜黄素,它们与纯姜黄素一样有效。基于致癌作用的多项临床研究,每日口服 3.6 克姜黄素对结直肠癌有效,并主张将其推进到 II 期临床研究。除了抗癌作用外,姜黄素在体外和体内临床前研究中对多种疾病状况也有疗效。本综述强调了姜黄素作为一种抗炎剂的重要性,并表明姜黄素的有益作用是通过过氧化物酶体增殖物激活受体-γ(PPAR-γ)的上调来介导的。

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