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青蒿素衍生物 SM934 治疗自身免疫性和炎症性疾病:治疗效果和分子机制。

Artemisinin derivative SM934 in the treatment of autoimmune and inflammatory diseases: therapeutic effects and molecular mechanisms.

机构信息

Laboratory of Immunopharmacology, State Key Laboratory of Drug Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, 201203, China.

University of Chinese Academy of Sciences, Beijing, 100049, China.

出版信息

Acta Pharmacol Sin. 2022 Dec;43(12):3055-3061. doi: 10.1038/s41401-022-00978-4. Epub 2022 Sep 1.

Abstract

Artemisinin and its derivatives are the well-known anti-malarial drugs derived from a traditional Chinese medicine. In addition to antimalarial, artemisinin and its derivatives possess distinguished anti-cancer, anti-oxidant, anti-inflammatory and anti-viral activities, but the poor solubility and low bioavailability hinder their clinical application. In the last decades a series of new water-soluble and oil-soluble derivatives were synthesized. Among them, we have found a water-soluble derivative β-aminoarteether maleate (SM934) that exhibits outstanding suppression on lymphocytes proliferation in immunosuppressive capacity and cytotoxicity screening assays with 35-fold higher potency than dihydroartemisinin. SM934 displays significant therapeutic effects on various autoimmune and inflammatory diseases, including systemic lupus erythematosus, antiphospholipid syndrome nephropathy, membranous nephropathy, rheumatoid arthritis, multiple sclerosis, inflammatory bowel disease, and dry eye disease. Here, we summarize the immunomodulatory effects, anti-inflammatory, anti-oxidative and anti-fibrosis activities of SM934 in disease-relevant animal models and present the probable pharmacological mechanisms involved in its therapeutic efficacy. This review also delineates a typical example of natural product-based drug discovery, which might further vitalize natural product exploration and development in pharmacotherapy.

摘要

青蒿素及其衍生物是源自中药的著名抗疟药物。除抗疟外,青蒿素及其衍生物还具有显著的抗癌、抗氧化、抗炎和抗病毒活性,但较差的溶解度和低生物利用度阻碍了其临床应用。在过去的几十年中,已经合成了一系列新的水溶性和油溶性衍生物。在这些衍生物中,我们发现了一种水溶性衍生物β-氨基青蒿琥酯马来酸盐(SM934),它在免疫抑制能力和细胞毒性筛选试验中对淋巴细胞增殖具有出色的抑制作用,其抑制活性比二氢青蒿素高 35 倍。SM934 在多种自身免疫性和炎症性疾病中显示出显著的治疗效果,包括系统性红斑狼疮、抗磷脂综合征肾病、膜性肾病、类风湿关节炎、多发性硬化症、炎症性肠病和干眼症。在这里,我们总结了 SM934 在相关疾病动物模型中的免疫调节作用、抗炎、抗氧化和抗纤维化活性,并提出了其治疗效果所涉及的可能药理学机制。本综述还描绘了一个基于天然产物的药物发现的典型例子,这可能进一步激发天然产物在药物治疗中的探索和开发。

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