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炎症靶向鬼臼噻吩素纳米药物通过 NF-κB 和 Notch1 通路减轻胶原诱导性关节炎。

Inflammation-Targeted Celastrol Nanodrug Attenuates Collagen-Induced Arthritis through NF-κB and Notch1 Pathways.

机构信息

Henan Provincial People's Hospital, People's Hospital of Zhengzhou University, Zhengzhou 450003, China.

PCFM Lab of Ministry of Education, School of Materials Science and Engineering, Sun Yat-Sen University, Guangzhou 510275, China.

出版信息

Nano Lett. 2020 Oct 14;20(10):7728-7736. doi: 10.1021/acs.nanolett.0c03279. Epub 2020 Sep 30.

Abstract

Rheumatoid arthritis (RA) is a systemic inflammatory disorder which can cause bone and cartilage damage leading to disability, yet the treatment remains unsatisfactory nowadays. Celastrol (Cel) has shown antirheumatic activity against RA. However, the frequent parenteral delivery and poor water solubility of Cel restrict its further therapeutic applications. Here, aiming at effectively overcoming the poor water solubility and short half-life of Cel to boost its beneficial effects for treating RA, we developed a polymeric micelle for Cel delivery based on a reactive oxygen species (ROS) sensitive polymer. Our results demonstrated that Cel may inhibit the repolarization of macrophages toward the pro-inflammatory M1 pheno-type via regulating the NF-κB and Notch1 pathways, which resulted in significantly decreased secretion of multiple pro-inflammatory cytokines to suppress the RA progression. Consequently, the Cel-loaded micelle effectively alleviated the major RA-associated symptoms including articular scores, ankle thickness, synovial inflammation, bone erosion, and cartilage degradation.

摘要

类风湿关节炎(RA)是一种全身性炎症性疾病,可导致骨骼和软骨损伤,从而导致残疾,但目前的治疗仍不尽如人意。雷公藤红素(Cel)已显示出抗风湿活性,可对抗 RA。然而,Cel 频繁的注射给药和较差的水溶性限制了其进一步的治疗应用。在这里,我们旨在通过开发一种基于活性氧(ROS)敏感聚合物的 Cel 递药聚合物胶束,有效克服 Cel 的低水溶性和短半衰期,以提高其治疗 RA 的有益效果。我们的研究结果表明,Cel 可能通过调节 NF-κB 和 Notch1 通路,抑制巨噬细胞向促炎 M1 表型的复极化,从而显著减少多种促炎细胞因子的分泌,抑制 RA 进展。因此,载 Cel 胶束有效缓解了 RA 相关的主要症状,包括关节评分、踝关节厚度、滑膜炎症、骨侵蚀和软骨降解。

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