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Both MMF and fumarate are believed to be responsible for the primary therapeutic effects of DMF through activation and inhibition of the transcription factors, Nrf2 ( via the agonism of the hydroxycarboxylic acid receptor 2 ( in vitro and in vivo immunologic actions of DMF ( in vitro causes a rise in the concentration of succinate ( in vivo by using global metabolomics profiling of blood plasma of patients with relapsing-remittent multiple sclerosis treated for 6 weeks with DMF