2022
DOI: 10.1016/j.jff.2022.105335
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The flavonoids extract from Okra flowers protects against DSS-induced colitis via regulating NF-κB signaling pathway and gut microbiota

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Cited by 4 publications
(6 citation statements)
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“…Compared with the MC group, the tight junction of the DOPL group was significantly restored (Figure I–K). Previous studies have shown that dietary flavonoids and phenolic compounds have a positive regulatory effect on the increased levels of tight junction proteins. , Our experiments confirmed this idea and indicated that DOP may improve the intestinal barrier by enhancing the tight junction protein.…”
Section: Discussionsupporting
confidence: 88%
“…Compared with the MC group, the tight junction of the DOPL group was significantly restored (Figure I–K). Previous studies have shown that dietary flavonoids and phenolic compounds have a positive regulatory effect on the increased levels of tight junction proteins. , Our experiments confirmed this idea and indicated that DOP may improve the intestinal barrier by enhancing the tight junction protein.…”
Section: Discussionsupporting
confidence: 88%
“…It is worth noting that the dilution concentration of RRTE in the ABTS-scavenging assay was up to 0, 10, 20, 40, 60, 80, 100, 120, 140, 160, 180, and 200 µg/mL, and -scavenging up to 100, 200, 300, 400, 500, 600, 700, 800, 900, and 1000 µg/mL in the DPPH-scavenging assay, which confirmed after pre-experiment. The human normal colon epithelial (NCM460) cells were purchased from ATCC (the United States) and cultured in DMEM medium containing 10% serum and 1% double antibody in a cell culture incubator at 37 • C with 5% CO 2 concentration [10].…”
Section: Determination Of the Antioxidant Capacity Of Rrtementioning
confidence: 99%
“…NCM460 cells were planted in 96-well plates at 5 × 10 3 cells/well; and after wall attachment, we added RRTE at a concentration gradient of 200-500 µg/mL for 12/24 h, and then 90 mg/mL DSS solution for 12 h. After the intervention was completed, 20 µL of MTT solution at a concentration of 5 mg/mL was added; and after incubation for 2-4 h, the solution in the wells was aspirated, DMSO solution (150 µL/well) was added and the solution was shaken for 15 min to dissolve the blue-violet crystals at the bottom, and the absorbance at 570 nm was determined [10].…”
Section: Cell Viability Assaymentioning
confidence: 99%
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