lignans and Autoimmune-Diseases

lignans has been researched along with Autoimmune-Diseases* in 2 studies

Other Studies

2 other study(ies) available for lignans and Autoimmune-Diseases

ArticleYear
Matairesinol ameliorates experimental autoimmune uveitis by suppression of IRBP-specific Th17 cells.
    Journal of neuroimmunology, 2020, 08-15, Volume: 345

    We investigated the effects of matairesinol (MAT) in the experimental autoimmune uveitis (EAU), a classical animal model of uveitis. We found that treatment with MAT could alleviate intraocular inflammation of EAU. Notably, Th17 cells in eyes of EAU mice could be predominantly restrained by MAT. Furthermore, MAT could inhibit Th17 differentiation in vitro. In addition, MAT inhibited the signaling of MAPK and ROR-γt, a pivotal transcription factor for Th17 cell differentiation in vitro and in vivo. Taken together, these results suggested that MAT had immune-suppressive effects on autoimmune inflammation through Th17 cells.

    Topics: Animals; Autoimmune Diseases; Eye Proteins; Female; Freund's Adjuvant; Furans; Lignans; Mice; Mice, Inbred C57BL; Retinol-Binding Proteins; Th17 Cells; Uveitis

2020
Occurrence of autoimmune antibodies to liver microsomal proteins associated with lethal hepatitis in LEC rats: effects of TJN-101 ((+)-(6S,7S,R-biar)- 5,6,7,8-tetrahydro-1,2,3,12-tetramethoxy-6,7-dimethyl-10,11- methylenedioxy-6-dibenzo[a,c]cyclooctenol)
    Toxicology letters, 1995, Volume: 76, Issue:1

    Long Evans Cinnamon (LEC) rats, that spontaneously develop hepatitis, were found to possess autoantibodies to liver microsomal proteins (anti-LM) before the development of hepatitis. Anti-LM antibody was assumed to appear in association with the lethal hepatitis in the LEC rats. Thus, the purpose of this study was to investigate the effects of an anti-hepatitis drug on the development of hepatitis and the occurrence of the antibody in LEC rats. Mortality, blood biochemical parameters and the titer of serum anti-LM antibody were measured. In control LEC rats, 4 of 8 rats died before 20 weeks of age. In rats treated with TJN-101 ((+)-(6S,7S,R-biar)-5,6,7,8-tetrahydro-1,2,3,12-tetramethoxy -6,7-dimethyl-10,11 - methylenedioxy-6-dibenzo[a,c]cyclooctenol), 4 of 7 rats died of hepatitis, but the time of death was delayed by 7-10 weeks compared to the control rats. The titer of the anti-LM antibody increased 3-7 weeks before death in the non-survivors in control and TJN-101-treated rats, supporting the idea that anti-LM antibody occurs in association with acute lethal hepatitis.

    Topics: Animals; Autoantibodies; Autoimmune Diseases; Body Weight; Cyclooctanes; Dioxoles; Enzyme-Linked Immunosorbent Assay; Female; Hepatitis, Animal; Lignans; Microsomes, Liver; Rats

1995