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In LPS-induced bone marrow macrophages and monosodium urate (MSU)-induced mouse arthritis models, andrographolide suppressed the activity of the NLRP3 inflammasome, and its mechanism in the treatment of gout mainly involved the downregulation of LPS-induced IKK, IB and NF-B phosphorylation to inhibit IL-1 release, reduce NLRP3 and pro-IL-1 protein expression, induce HO-1 expression, reduce reactive oxygen species generation, reduce LPS/MSU-induced NLRP3 inflammasome assembly and cysteine Asparaginase-1 formation and attenuate MSU phagocytosis ( 5.4 Multiple sclerosis Multiple sclerosis (MS) is an autoimmune disease in the central nervous system, and its main pathogenesis is the dysfunction of dendritic cells, resulting in an immune response to myelin damage ( in vitro , andrographolide interferes with T-cell proliferation and cytokine release in response to allogeneic stimulation, influences dendritic cell maturation and suppresses antigen presentation to T cells