Application of ar-turmerone in preparation of product for preventing and treating ulcerative colitis and regulating intestinal florae
A technique for regulating intestinal flora in ulcerative colitis, applied in the field of medicine, to achieve the effect of reducing the degree of inflammation, reducing inflammatory factors, and adjusting intestinal disorders
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Embodiment 1
[0044] Example 1 The improvement of DSS-induced ulcerative colitis in mice by the length of mouse intestinal colon to cecum detected by aromatic curcumin
[0045] 1. Experimental method
[0046]Embodiment Experimental animals are divided into 7 groups at random, are respectively: normal control group (Con), DSS group, turmeric essential oil group (DSS+turmeric essential oil, J, 2.4mg / kg / day), positive drug group (DSS+mesalazine , M, 40mg / kg / day), low-dose aromatic curcumone group (DSS+aromatic curcumone, FL, 10mg / kg / day), medium-dose aromatic curcumone group (DSS+aromatic curcumone, FM, 20mg / kg / day ) and high-dose aromatic curcumone group (40mg / kg / day) with 5 rats in each group.
[0047] Each group was administered continuously for 2 weeks, and 350 mg / kg was administered orally every day. In the first week of administration, except the normal group, the rest of the groups were free to drink DSS solution for one week to prepare the intestinal ulcer model. On the 8th day, the ...
Embodiment 2
[0050] Example 2 Effect of Aroma Curcumone on DSS-Induced Mice Intestinal Tissue Colonic Mucosal Cell Injury
[0051] 1. Experimental method
[0052] The experimental grouping and dosing regimen of this example are the same as in Example 1. After the administration of the mice, the mice were killed by spinal dislocation, and the complete colon tissues were taken out to make paraffin sections and stained with HE. The operation steps included: fixing the colon tissues Soak in 4% paraformaldehyde solution for 6 hours → dehydration: gradually increase from low-concentration alcohol to high-concentration alcohol, put it in 50%, 70%, 80% and 95% alcohol for 12-24 hours each, 100% alcohol for 2-3 hours, then put in xylene and alcohol for half an hour, and then put in xylene until the specimen is transparent → Wax penetration: move the colon tissue into xylene plus paraffin, and put it in a 60°C incubator After half an hour, move it into paraffin to make the paraffin penetrate into t...
Embodiment 3
[0055] Example 3 Effect of Aroma Curcumone on DSS-induced Inflammatory Response in Mouse Colon Tissue
[0056] 1. Experimental method
[0057] The experimental grouping and dosing scheme of this example are the same as in Example 1 and Example 2. After the administration, the mouse spine was killed, and the complete colonic tissue was taken out to make paraffin sections, and immunohistochemical or immunofluorescent staining was performed on the sections, and then The expression of the inflammatory factor TNF-α in the colonic mucosa was determined by immunohistochemistry or immunofluorescence staining, and the experimental data were expressed as Mean ± SD. All experimental data were statistically analyzed using GraphPad Prism7.04 software. Between parameters were tested by ANOVA, P<0.05 was considered to be statistically different.
[0058] Immunohistochemical staining was performed on tissue paraffin sections to detect the expression level of inflammatory factor TNF-α. The p...
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