Abstract
As a traditional Mongolian medicine, Sendeng-4 (SD) has been widely used to treat rheumatoid arthritis (RA) in Inner Mongolia and exhibits a good curative effect. Unfortunately, due to geographical factors, it is difficult to popularize this drug throughout the whole country, and the mechanism of action of SD has been unclear. In this study, a serum metabolite profile analysis was performed to identify potential biomarkers associated with adjuvant-induced RA and investigate the mechanism of action of SD. Ultraperformance liquid chromatography coupled with quadrupole time-of-flight mass spectrometry (UPLC-Q-TOF-MS) was performed for the metabonomics analysis. K nearest neighbor (KNN) models were established in both positive and negative spectra for classifying data from the control, model, and SD administration groups. Accuracy rate for classification was 95.8% in positive ion mode and 91.7% in negative ion mode. Orthogonal partial least squares discriminant analysis (OPLS-DA) enabled the identification of 12 metabolites as potential biomarkers of adjuvant-induced RA. After treatment with SD, the levels of uridine triphosphate, calcitroic acid, dynorphin B (6-9), and docosahexaenoic acid were restored to normal, indicating that SD likely ameliorated RA by regulating the levels of these biomarkers. This study identified early biomarkers of RA and elucidated the underlying mechanism of action of SD, which is worth further investigation for development as a clinical therapy.
Highlights
Rheumatoid arthritis (RA) is an autoimmune inflammatory disease
This study demonstrated that the combination of multispectral (MS) MRI analysis method and K nearest neighbor (KNN) classification provided the quantitative tool for the BeltaBLV [14]
SD showed a good therapeutic effect on RA rats induced by adjuvant
Summary
Rheumatoid arthritis (RA) is an autoimmune inflammatory disease. The main clinical manifestations are chronic, symmetrical, and synovial arthritis and extra-articular disease. The treatment of RA mainly relies on Western medicine such as the nonsteroidal drug, diclofenac [2]; antirheumatic drug, methotrexate [3]; and glucocorticoid drug, dexamethasone [4]. These Western medicines are highly efficacious but are accompanied by toxic side effects. Western medicine can only temporarily relieve or eliminate the pain and cannot cure RA fundamentally
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