具有抗炎活性的中药对脂肪酸合酶的抑制作用
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1.1)中国科学院大学生命科学学院,北京 100049;2.2)北京泰德制药股份有限公司,北京 100176

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Q55;R932

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Traditional Chinese medicines with anti-inflammatory functions and their inhibitory effects on fatty acid synthase *
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1.1)College of Life Sciences, University of Chinese Academy of Sciences, Beijing 100049, China;2.2)Beijing Tide Pharmaceutical Co., Ltd., Beijing 100176, China

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    摘要:

    随着肥胖及其相关疾病的患病率不断上升,肥胖并发的慢性炎症已成为一个不容忽视的公共卫生问题,迫切需要针对肥胖相关慢性炎症新的治疗方案和干预策略。脂肪酸合酶(Fatty acid synthase,FAS)是一种多功能复合酶,是治疗肥胖、糖尿病、非酒精性脂肪肝、炎症和癌症的潜在靶点。持续的炎症反应是潜在的危险因素。一些关键的炎症标志物与肥胖密切相关,其中特别是FAS抑制剂的研究受到越来越多的关注。在我国,中药已广泛被应用于炎症的治疗,其中有多种中药对FAS表现出强抑制作用。本文综述了中药FAS抑制剂的结构和活性特点,对于研发中药FAS抑制剂治疗炎症提供了依据。

    Abstract:

    As the prevalence of obesity and related diseases continues to rise, obesity accompanied chronic inflammation becomes a non-neglect public health problem. Innovative treatment options and strategies for obesity-related chronic inflammation are urgently needed. Fatty acid synthase (FAS) is a multiple enzyme complex which has been recognized as a potential therapeutic target for obesity, inflammation, diabetes, non-alcohol fatty liver disease (NAFLD), and cancer. Research on FAS inhibitors has attracted increasing attention in recent years. Several key inflammatory markers have been consistently associated with obesity, which suggests that a persistent inflammatory response is a potentially modifiable risk factor. In China, traditional Chinese medicines (TCMs) have been applied clinically to treat inflammation. Among them there are several TCMs with strong inhibitory effect on FAS. This brief review aims at summarizing literatures concerning the recognized role of FAS as a biomarker and therapeutic target in obesity and related inflammation as well as providing evidence to support the anti-inflammation potential of TCMs with FAS inhibitory activities. FAS has emerged as a crucial target in anti-obesity therapies, and FAS inhibition might contribute to the treatment of inflammation.

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黄文元,王红军,AMANTAY Alzhan,田维熙,马晓丰.具有抗炎活性的中药对脂肪酸合酶的抑制作用[J].生物化学与生物物理进展,2020,47(8):809-817

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历史
  • 收稿日期:2020-05-13
  • 最后修改日期:2020-05-13
  • 接受日期:2020-05-19
  • 在线发布日期: 2020-11-26
  • 出版日期: 2020-08-20