Li Ziyu, Zhang Qiuyan, Gao Yuhe, Wan Fang, Wang Yincang, Hou Bin, Cui Wenwen, Wang Yanan, Feng Wei, Hou Yunlong
Suzhou TCM Hospital Affiliated to Nanjing University of Chinese Medicine, Suzhou, People's Republic of China.
New Drug Evaluation Center, Shijiazhuang Yiling Pharmaceutical Co., Ltd, Shijiazhuang, People's Republic of China.
J Inflamm Res. 2024 Jul 6;17:4389-4403. doi: 10.2147/JIR.S461093. eCollection 2024.
The LuoBiTong (LBT) capsule, a novel traditional Chinese medicine formulation, is currently in Phase III clinical trials. Preliminary preclinical and Phase II clinical studies suggest its efficacy and safety in treating rheumatoid arthritis (RA). However, the underlying mechanisms of its action remain to be elucidated.This research aims to explore the effects and mechanisms of LBT in conjunction with a maintenance dose of methotrexate (M-MTX) on RA.
A Collagen-Induced Arthritis (CIA) mouse model was used to evaluate the anti-RA effects of LBT combined with M-MTX. Assessments included foot swelling, arthritis scoring, serum inflammatory factor analysis, and histopathological examination of the foot. These effects were compared with those of high-dose MTX (H-MTX). Network pharmacology was employed to construct a compound-target network for RA, based on drug composition, to predict its potential mechanism of action. Flow cytometry, Western Blot, and immunohistochemical analyses in animal models identified multiple inflammatory pathways targeted by LBT to augment the anti-RA effects of MTX.
The study revealed that LBT combined with M-MTX significantly alleviated CIA-induced arthritis without adverse effects. The combination of LBT and M-MTX showed similar or superior efficacy in regulating macrophage polarization, NF-κB, MAPK signaling pathways, and in the suppression of TH-17 expression in proinflammatory cells. These findings suggest that LBT may exert a multi-pathway therapeutic effect in RA treatment. The predicted pharmacological targets and mechanisms align well with this hypothesis.
LBT, when combined with MTX, enhances the anti-RA effect by targeting multiple inflammatory pathways, demonstrating significant therapeutic potential.
洛必通(LBT)胶囊是一种新型中药制剂,目前正处于III期临床试验阶段。初步的临床前和II期临床研究表明其在治疗类风湿性关节炎(RA)方面的有效性和安全性。然而,其作用的潜在机制仍有待阐明。本研究旨在探讨LBT联合甲氨蝶呤维持剂量(M-MTX)对RA的影响及其机制。
采用胶原诱导性关节炎(CIA)小鼠模型评估LBT联合M-MTX的抗RA作用。评估内容包括足肿胀、关节炎评分、血清炎症因子分析以及足部组织病理学检查。将这些作用与高剂量甲氨蝶呤(H-MTX)的作用进行比较。基于药物成分,运用网络药理学构建RA的化合物-靶点网络,以预测其潜在作用机制。通过对动物模型进行流式细胞术、蛋白质印迹法和免疫组织化学分析,确定LBT靶向的多种炎症途径,以增强MTX的抗RA作用。
研究表明,LBT联合M-MTX可显著减轻CIA诱导的关节炎,且无不良反应。LBT与M-MTX联合使用在调节巨噬细胞极化、NF-κB、MAPK信号通路以及抑制促炎细胞中TH-17表达方面显示出相似或更好的疗效。这些发现表明,LBT在RA治疗中可能发挥多途径治疗作用。预测的药理靶点和机制与这一假设高度吻合。
LBT与MTX联合使用时,通过靶向多种炎症途径增强抗RA作用,显示出显著的治疗潜力。