Unveiling the Nexus: Cellular Metabolomics Unravels the Impact of Estrogen on Nicotinamide Metabolism in Mitigating Rheumatoid Arthritis Pathogenesis

• Published in: Metabolites Vol. 14; no. 4; p. 214
• Main Authors: Malik, Swati, Chakraborty, Debolina, Agnihotri, Prachi, Kumar, Vijay, Biswas, Sagarika
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 01.04.2024
• Subjects: 1-methylnicotinamide; 17β-Estradiol; Analysis; Care and treatment; Cell culture; Chromatography; Diagnosis; Estrogen; Estrogens; Females; Fibroblasts; Gelatinase B; Health aspects; Inflammation; Kinases; Liquid chromatography; Mass spectrometry; Mass spectroscopy; Metabolism; Metabolites; Metabolomics; Molecular weight; Niacinamide; Nicotinamide; nicotinate and nicotinamide metabolism; Oxidative stress; Pathogenesis; Physiological aspects; Retention; Rheumatoid arthritis; Rheumatology; Scientific imaging; Stat1 protein; synovial fibroblast; India; estrogen; metabolomics; synovial fibroblast; rheumatoid arthritis; 1-methylnicotinamide; nicotinate and nicotinamide metabolism
• ISSN: 2218-1989; 2218-1989
• DOI: 10.3390/metabo14040214

Rheumatoid arthritis (RA) is a metabolic joint disorder influenced by hormonal regulation, notably estrogen, which plays a cytoprotective role against inflammation. While estrogen's impact on RA pathogenesis has been studied, the altered metabolite expression under estrogen's influence remains unexplored. This study investigated the changes in the metabolome of synovial fibroblasts isolated from RA patients under 17β-estradiol (E2) using the liquid chromatography with tandem mass spectrometry (LC-MS/MS) approach followed by multivariate and biological pathway analysis along with in vitro validation. Results identified 3624 / , among which eight metabolites were significant ( < 0.05). Nicotinate and nicotinamide metabolism was found to be highly correlated with the treatment of E2, with metabolites NAD and 1-methynicotinamide (1-MNA) upregulated by E2 induction in RA-FLS. PharmMapper analysis identified potential gene targets of 1-MNA, which were further matched with RA gene targets, and thus, STAT1, MAPK14, MMP3, and MMP9 were concluded to be the common targets. E2 treatment affected the expression of these gene targets and ameliorated the development of oxidative stress associated with RA inflammation, which can be attributed to increased concentration of 1-MNA. Thus, an LC-MS/MS-based metabolomics study revealed the prominent role of estrogen in preventing inflammatory progression in RA by altering metabolite concentration, which can support its therapeutic capacity in remitting RA.