Mechanism of Fructus Mume Pills Underlying Their Protective Effects in Rats with Acetic Acid-Inducedulcerative Colitis via the Regulation of Inflammatory Cytokines and the VEGF-PI3K/Akt-eNOS Signaling Pathway

<div>UPLC profiles of standards and FMP aqueous extract. (a) Chromatograms of citric acid, phellodendron hydrochloride, coptisine hydrochloride, berberine hydrochloride, ferulic acid, lobetyolin, cinnamic acid, hydroxy-<i>α</i>-sanshool, 6-gingerol, <i>ß</i>-asarum ether, and <i>a</i>-asarum standards under 285 nm detection wavelength. S1: standard chromatograms, S2 : FMP chromatograms. (b) Chromatograms of benzoylaconine, benzoyl neoaconitine, and benzoyl hypoaconitine standards under 235 nm detection wavelength. S3: standard chromatograms, S4 : FMP chromatogram.</div>

Evidence-Based Complementary and Alternative Medicine

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Figure 1: Mechanism of Fructus Mume Pills Underlying Their Protective Effects in Rats with Acetic Acid-Inducedulcerative Colitis via the Regulation of Inflammatory Cytokines and the VEGF-PI3K/Akt-eNOS Signaling Pathway 

Figure 1 | Mechanism of Fructus Mume Pills Underlying Their Protective Effects in Rats with Acetic Acid-Inducedulcerative Colitis via the Regulation of Inflammatory Cytokines and the VEGF-PI3K/Akt-eNOS Signaling Pathway 