“…FO inhibited the subunits of NF-κB entering the nucleus and decreased the NF-κB level in the nucleus, and NF-κB maintained in the cytoplasm as an inactive form, which contributed to decreased inflammatory cytokines. It has been reported that FO supplementation increased EPA and DHA in serum [39], and DHA performed the neuroprotective effect on hippocampal neurons by its antioxidant effect, preventing inflammatory cytokine expression, and anti-apoptotic potential [40]. FO supplementation is also liable to exert effects on the DRGs directly.…”