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We have identified that high\u2010dose wogonin (50 or 100 mg\/kg) could inhibit the growth of transplanted tumours by directly inducing tumour apoptosis and promoting <jats:styled-content style=\"fixed-case\">DC<\/jats:styled-content>, T and <jats:styled-content style=\"fixed-case\">NK<\/jats:styled-content> cell recruitment into tumour tissues to enhance immune surveillance. However, wogonin (20\u201350 \u03bcM) <jats:italic>ex vivo<\/jats:italic> prevents inflammation by inhibiting <jats:styled-content style=\"fixed-case\">NF<\/jats:styled-content>\u2010\u03baB and Erk signalling of macrophages and epithelial cells. It is elusive whether high\u2010dose wogonin promotes or prevents inflammation. To investigate the effects of high\u2010dose wogonin on murine colitis induced by dextran sodium sulphate (<jats:styled-content style=\"fixed-case\">DSS<\/jats:styled-content>), mice were co\u2010treated with <jats:styled-content style=\"fixed-case\">DSS<\/jats:styled-content> and various doses of wogonin. Intraperitoneal administration of wogonin (100 mg\/kg) exacerbated <jats:styled-content style=\"fixed-case\">DSS<\/jats:styled-content>\u2010induced murine colitis. More <jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>4<jats:sup>+<\/jats:sup> <jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>44<jats:sup>+<\/jats:sup> and <jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>8<jats:sup>+<\/jats:sup> <jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>44<jats:sup>+<\/jats:sup> cells were located in the inflamed colons in the wogonin (100 mg\/kg) treatment group than in the other groups. Frequencies of <jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>4<jats:sup>+<\/jats:sup> <jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>25<jats:sup>+<\/jats:sup> <jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>127<jats:sup>\u2212<\/jats:sup> and <jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>4<jats:sup>+<\/jats:sup> <jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>25<jats:sup>+<\/jats:sup> Foxp3<jats:sup>+<\/jats:sup> cells in the colons and spleen respectively, were reduced by wogonin treatment. <jats:italic>Ex vivo<\/jats:italic> stimulations with high\u2010dose wogonin (50\u2013100 \u03bcg\/ml equivalent to 176\u2013352 \u03bcM) could synergize with <jats:styled-content style=\"fixed-case\">IL<\/jats:styled-content>\u20102 to promote the functions of <jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>4<jats:sup>+<\/jats:sup> and <jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>8<jats:sup>+<\/jats:sup> cells. However, regulatory T cell induction was inhibited. Wogonin stimulated the activation of <jats:styled-content style=\"fixed-case\">NF<\/jats:styled-content>\u2010\u03baB and Erk but down\u2010regulated <jats:styled-content style=\"fixed-case\">STAT<\/jats:styled-content>3 phosphorylation in the <jats:styled-content style=\"fixed-case\">CD<\/jats:styled-content>4<jats:sup>+<\/jats:sup> T cells. Wogonin down\u2010regulated Erk and <jats:styled-content style=\"fixed-case\">STAT<\/jats:styled-content>3\u2010Y705 phosphorylation in the regulatory T cells but promoted <jats:styled-content style=\"fixed-case\">NF<\/jats:styled-content>\u2010\u03baB and <jats:styled-content style=\"fixed-case\">STAT<\/jats:styled-content>3\u2010S727 activation. Our study demonstrated that high\u2010dose wogonin treatments would enhance immune activity by stimulating the effector T cells and by down\u2010regulating regulatory T cells.<\/jats:p>","DOI":"10.1111\/jcmm.12964","type":"journal-article","created":{"date-parts":[[2016,9,19]],"date-time":"2016-09-19T11:56:47Z","timestamp":1474286207000},"page":"286-298","source":"Crossref","is-referenced-by-count":19,"title":["High\u2010dose wogonin exacerbates <scp>DSS<\/scp>\u2010induced colitis by up\u2010regulating effector T cell function and inhibiting Treg cell"],"prefix":"10.1111","volume":"21","author":[{"given":"Weiming","family":"Xiao","sequence":"first","affiliation":[{"name":"Department of Gastroenterology Affiliated hospital Yangzhou University Yangzhou China"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Min","family":"Yin","sequence":"additional","affiliation":[{"name":"Department of Gastroenterology Affiliated hospital Yangzhou University Yangzhou 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