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新型微管调节溴化紫堇碱类似物的强效抗炎活性。

Potent anti-inflammatory activity of novel microtubule-modulating brominated noscapine analogs.

机构信息

Division of Infectious Diseases, Emory University School of Medicine, Atlanta, Georgia, United States of America.

出版信息

PLoS One. 2010 Feb 11;5(2):e9165. doi: 10.1371/journal.pone.0009165.

Abstract

Noscapine, a plant-derived, non-toxic, over-the-counter antitussive alkaloid has tubulin-binding properties. Based upon the structural resemblance of noscapine to colchicine, a tubulin-binding anti-inflammatory drug, noscapine and its semi-synthetic brominated analogs were examined for in vitro anti-inflammatory activity. Brominated noscapine analogs were found to inhibit cytokine and chemokine release from macrophage cell lines but did not affect cell viability. Brominated noscapine analogs demonstrated anti-inflammatory properties in both TLR- and non-TLR induced in vitro innate immune pathway inflammation models, mimicking septic and sterile infection respectively. In addition, electron microscopy and immunoblotting data indicated that these analogs induced robust autophagy in human macrophages. This study is the first report to identify brominated noscapines as innate immune pathway anti-inflammatory molecules.

摘要

纳可沙平,一种源自植物的、无毒的、非处方镇咳生物碱,具有微管结合特性。基于纳可沙平与秋水仙碱(一种微管结合的抗炎药物)的结构相似性,对纳可沙平和其半合成溴化类似物进行了体外抗炎活性研究。研究发现,溴化纳可沙平类似物可抑制巨噬细胞系细胞因子和趋化因子的释放,但不影响细胞活力。溴化纳可沙平类似物在 TLR 和非 TLR 诱导的体外先天免疫途径炎症模型中均表现出抗炎特性,分别模拟脓毒症和无菌感染。此外,电子显微镜和免疫印迹数据表明,这些类似物可诱导人巨噬细胞中强烈的自噬。本研究首次报道了溴化纳可沙平是先天免疫途径抗炎分子。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2392/2820095/566de0ee8f8f/pone.0009165.g001.jpg

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