Inflammation-Targeted Celastrol Nanodrug Attenuates Collagen-Induced Arthritis through NF-κB and Notch1 Pathways.
Lemei AnZhanrong LiLiuqi ShiLiujun WangYong WangLin JinXin-Tao ShuaiHuayang FengPublished in: Nano letters (2020)
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.
Keyphrases
- rheumatoid arthritis
- oxidative stress
- disease activity
- reactive oxygen species
- ankylosing spondylitis
- diabetic rats
- interstitial lung disease
- cancer therapy
- drug delivery
- signaling pathway
- bone mineral density
- rheumatoid arthritis patients
- cell proliferation
- dna damage
- nuclear factor
- lps induced
- systemic lupus erythematosus
- extracellular matrix
- cell death
- soft tissue
- physical activity
- sleep quality
- bone loss
- high glucose
- optical coherence tomography
- bone regeneration
- depressive symptoms