关节炎
肿瘤坏死因子α
医学
类风湿性关节炎
mTORC1型
体内
炎症
佐剂
药理学
胶原性关节炎
免疫学
PI3K/AKT/mTOR通路
内科学
化学
信号转导
生物
生物化学
生物技术
作者
Jian Zhong,Taotao Ma,Cheng Huang,Huanzhong Liu,Zhaolin Chen,Lu Cao,Xiaohui Li,Jun Li
标识
DOI:10.1142/s0192415x14500578
摘要
Macrophages play a crucial role in rheumatoid arthritis (RA). Their activation is the initial step of RA. This study was designed to detect the effects of total flavonoids from Litsea coreana Levl. (TFLC) on the complete Freund's adjuvant-induced (CFA-induced) arthritis (AA) in rats and to explore whether inflammatory cytokines were induced by the IRE1/mTORC1/TNF-α-dependant mechanism in peritoneal macrophages. In vivo, our data indicated that TFLC (100, 200 mg/kg, i.g. × 10 days) could significantly suppress secondary paw swelling and serum levels of TNF-α and IL-1β. Histopathological figures showed that TFLC treatment improved the morphologic changes of articular cartilages and synovium. Results of RT-PCR and western blotting demonstrated that TFLC suppressed expression of 78-KD glucose regulated protein (GRP78), X-box binding protein 1 (XBP1), mTOR complex 1 (mTORC1) and TNF-α in peritoneal macrophages of AA rats. Collectively, these results indicate that TFLC is able to ameliorate adjuvant-induced arthritis in a dose-dependent manner by suppressing the IRE1/mTORC1/TNF-α-regulated inflammatory response initiated in peritoneal macrophages.
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