2018
DOI: 10.1016/j.intimp.2018.04.010
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Emodin ameliorates ulcerative colitis by the flagellin-TLR5 dependent pathway in mice

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Cited by 42 publications
(27 citation statements)
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“…It is reported that emodin (5, 10 and 20 mg/kg) treatment alleviates the symptoms and decreases the level of anti-flagellin in serum and suppresses the expressions of TLR5 and NF-κBp65 in colon of DSS-induced UC mice. Moreover, in vitro, emodin treatment inhibits the nuclear translocation of NF-κBp65 and decreases the release of IL-8 in flagellin-stimulated HT-29 cells via down-regulating the expressions of TLR5 and MyD88, up-regulating the expression of IκB [92]. Chrysophanol (5 mg/kg) treatment decreases the activation of NF-κBp65 and caspase-1 in DSS-treated colon tissue and LPS-stimulated murine peritoneal macrophages, which contributes to attenuation of overall clinical scores and various pathological markers of colitis via against inflammatory injury [93].…”
Section: Detoxificating and Purgative Medicinementioning
confidence: 93%
“…It is reported that emodin (5, 10 and 20 mg/kg) treatment alleviates the symptoms and decreases the level of anti-flagellin in serum and suppresses the expressions of TLR5 and NF-κBp65 in colon of DSS-induced UC mice. Moreover, in vitro, emodin treatment inhibits the nuclear translocation of NF-κBp65 and decreases the release of IL-8 in flagellin-stimulated HT-29 cells via down-regulating the expressions of TLR5 and MyD88, up-regulating the expression of IκB [92]. Chrysophanol (5 mg/kg) treatment decreases the activation of NF-κBp65 and caspase-1 in DSS-treated colon tissue and LPS-stimulated murine peritoneal macrophages, which contributes to attenuation of overall clinical scores and various pathological markers of colitis via against inflammatory injury [93].…”
Section: Detoxificating and Purgative Medicinementioning
confidence: 93%
“…Emodin downregulated the activation of NF-κB in a dose-dependent manner in SW1990 and PANC-1 cells (65,70,104). In flagellin-stimulated HT-29 cells, it was revealed that emodin downregulated the expression of toll-like receptor (TLR)5 and myeloid differentiation primary response 88 (MyD88), upregulated the expression of IκB, inhibited the nuclear translocation of NF-κB p65 and reduced the production of IL-8 (172). Pre-treatment of U87MG cells with emodin also significantly reduced NF-κB activation in a hyaluronic acid-induced cell invasion model in vitro (120).…”
Section: Inflammation and Immunomodulation [Tnf-α/nuclear Factor к-Light-chain-enhancer Of Activated B Cells (Nf-кb) Pathway]mentioning
confidence: 99%
“…Emodin was found to induce autophagy in L02 human hepatocytes by inhibiting PI3K/AKT/mTOR signaling pathway [29]. Emodin was found to protect mice from DSS-induced colitis via the regulation of TLR5/NF-κB signaling pathway [30], and significantly inhibit LPS-mediated NF-κB activation and DNA binding activity in RAW264.7 cells [31]. This is consistent with our computer-based research, and indicates that emodin can regulate PI3K-Akt signaling pathway to exert anti-inflammatory effects.…”
Section: Figure 7 Components-targets-pathways Network Of Caulis Sargentodoxaementioning
confidence: 99%