Potent Anti-Inflammatory Activity of Novel Microtubule-Modulating Brominated Noscapine Analogs

被引:41
|
作者
Zughaier, Susu [1 ]
Karna, Prasanthi [2 ]
Stephens, David [1 ]
Aneja, Ritu [2 ]
机构
[1] Emory Univ, Sch Med, Div Infect Dis, Atlanta, GA 30322 USA
[2] Georgia State Univ, Dept Biol, Atlanta, GA USA
来源
PLOS ONE | 2010年 / 5卷 / 02期
关键词
CANCER-CELLS; UNDERGO APOPTOSIS; IMMUNE-RESPONSES; PERTURB MITOSIS; BREAST-CANCER; AUTOPHAGY; AGENT; MACROPHAGES; BINDING; INNATE;
D O I
10.1371/journal.pone.0009165
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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 semisynthetic 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.
引用
收藏
页数:11
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