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In the animal study, SFN-treated BTBR mice reduced Th17 immune responses (STAT3, RORC, IL-17 A, and IL-23R expression in CD4+ T cells) as well as oxidative stress parameters in neutrophils/cerebellum (NF-B, iNOS, and lipid peroxides) ( in vitro study ( ex vivo treatment by reducing the NF-B signaling, thereby reversing LPS-induced inflammation and nitrative stress in PBMCs ( ex vivo treatment decreased pro-inflammatory gene expression induced by LPS in human PBMCs ( in vitro study, oral administration of SFN decreased mRNA levels of pro-inflammatory markers in PBMCs from ASD patients (74)

epithelial proliferative UC), patients with mixed UC (subtype B), and patients with significant immune cell and proinflammatory characteristics (subtype C

doi:10.1016/j.drudis.2024.103914 8