Application of short-chain fatty acid in prevention or/and treatment of liver injury
A technology for short-chain fatty acids and liver damage, applied in the field of medicine, can solve the problems of high requirements for storage conditions, unclear effector molecules, and complicated extraction methods, and achieves significant prevention and treatment effects, low cost, and improvement of intestinal epithelial barrier effects.
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Embodiment 1
[0038] The influence of embodiment 1 propionic acid on alcoholic liver injury
[0039] 1. Determination of the effect of propionic acid on the survival rate of hepatocytes exposed to alcohol
[0040] It should be noted that in the present invention, the experimental cells are human hepatoma cells HepG2, and the medium used for cell culture is Hyclone containing 10% fetal bovine serum and 1% double antibody (penicillin 100U / mL, streptomycin 100 μg / mL). High glucose DMEM medium.
[0041] The specific measurement method is as follows:
[0042] After the recovery of HepG2 cells, after passage once, the cells in the logarithmic growth phase were collected and inoculated in a 96-well plate at a concentration of 5,000 cells per well, and placed at 37°C, 5% CO 2 Incubate overnight in the incubator. In the experiment, a blank group, a negative control group and an administration group were set up, with 5 duplicate wells in each group, the original medium was sucked and discarded, th...
Embodiment 2
[0090] The influence of embodiment 2 butyric acid on alcoholic liver injury
[0091] 1. Determination of the effect of butyric acid on the survival rate of hepatocytes exposed to alcohol
[0092] The specific assay method is described in Example 1.
[0093] 2. Determination of the effect of butyric acid on alcoholic liver injury model mice
[0094] 2.1 Construction of mouse alcoholic liver injury model (NIAAA method)
[0095] Forty-eight 8-week-old male C57BL / 6 (body weight > 20g) mice of SPF grade were randomly divided into 3 groups: blank control group (Control), alcohol model group (EtOH), supplemented with 100mM sodium butyrate Modules (EtOH+B), 12 in each group. The specific modeling and sampling methods are as described in Example 1.
[0096] 2.2 Determination of liver index
[0097] The specific assay method is described in Example 1.
[0098] 2.3 Determination of short-chain fatty acids in intestinal contents and liver tissue
[0099] The specific assay method i...
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