Pharmacological and clinical properties of curcumin

Christopher S Beevers, Shile Huang
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引用次数: 69

Abstract

The polyphenol natural product curcumin has been the subject of numerous studies over the past decades, which have identified and characterized the compound's pharmacokinetic, pharmacodynamic, and clinical pharmacological properties. In in vitro and in vivo model systems, curcumin displays potent pharmacological effects, by targeting many critical cellular factors, through a diverse array of mechanisms of action. Despite this tremendous molecular versatility, however, the clinical application of curcumin remains limited due to poor pharma- cokinetic characteristics in human beings. The current trend is to develop and utilize unique delivery systems, chemical derivatives, and chemical analogs to circumvent these pharmaco- logical obstacles, in order to optimize the conditions for curcumin as a chemopreventive and chemotherapeutic agent in diseases such as cancer, diabetes, obesity, Alzheimer's disease, and inflammatory disorders. The present work seeks to review recent studies in the basic pharma-
姜黄素的药理和临床性质
在过去的几十年里,多酚天然产物姜黄素一直是众多研究的主题,这些研究已经确定并表征了该化合物的药代动力学、药效学和临床药理学特性。在体外和体内模型系统中,姜黄素通过多种作用机制靶向许多关键细胞因子,显示出强大的药理作用。然而,尽管姜黄素具有巨大的分子多样性,但由于其在人体中的药物协同动力学特性较差,其临床应用仍然受到限制。目前的趋势是开发和利用独特的递送系统、化学衍生物和化学类似物来绕过这些药理学障碍,以优化姜黄素作为癌症、糖尿病、肥胖、阿尔茨海默病和炎症性疾病等疾病的化学预防和化学治疗药物的条件。目前的工作旨在回顾最近的研究在基础制药
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