Application of a strain of Lactobacillus plantarum in the preparation of a composition for alleviating chronic inflammation in the body
A technology of Lactobacillus plantarum and chronic inflammation, which is applied in the field of microorganisms, can solve the problems of limited chronic inflammation, differences in the effect of different strains, and obvious differences in individual intestinal flora and physiological state, so as to relieve chronic inflammation, prevent diseases, and achieve good health. The effect of stability
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Embodiment 1
[0035] The strain provided by the present invention has been identified as belonging to Lactobacillus plantarum, named as 1701 strain, and was preserved in the General Microorganism Culture Collection Center of China Microorganism Culture Collection Management Committee on October 23, 2019, and the microorganism preservation number is CGMCC NO.18728.
[0036] The strain provided by the present invention is isolated by the inventor from a yogurt powder sample collected from the countryside of Shigatse City, Tibet Autonomous Region of my country.
[0037] The 16S rRNA gene sequence of the strain Lactobacillus plantarum 1701 of the present invention is shown in SEQ ID NO: 1.
Embodiment 2
[0039] Kunming mice were reared at a temperature of 21±2°C, a humidity of 30-70%, 12 hours of alternating light, and free access to mouse maintenance feed and drinking water. After being reared for 1 week in Kunming, the mice were sacrificed by removing their cervical vertebrae, and the spleen of the mice was taken aseptically, and crushed with a sterile glass syringe core. The lysis was terminated with sterile Hank's solution of % fetal bovine serum, centrifuged at 1000 rpm for 5 min at 4° C., and the pellet was resuspended in 5 mL of RPMI-1640 medium containing 10% fetal bovine serum. The cells were stained with trypan blue and counted on a hemocytometer to calculate the number of viable cells and the percentage of viable cells. Adjust the cell concentration to 5 × 10 6 cells / mL.
[0040]After the second-generation activation of the strain Lactobacillus plantarum 1701 of the present invention and the reference commercial strain Lactobacillus rhamnosus GG (LGG), the bacter...
Embodiment 3
[0046] The spleen lymphocyte suspension was prepared according to the preparation method of mouse spleen lymphocytes in Example 2, and the cell concentration was adjusted to 5×10 6 cells / mL.
[0047] After the second-generation activation of the strain Lactobacillus plantarum 1701 of the present invention and the reference commercial strain Lactobacillus rhamnosus GG (LGG), the bacterial concentration was adjusted to 1×10 7 CFU / mL.
[0048] The cell suspension was added to a 96-well cell culture plate, with 5 replicates per treatment, and divided into zero adjustment group (cell culture medium), blank control group (cell culture medium + cell suspension), and bacterial treatment group (cell culture medium + Cell suspension + bacterial suspension 1×10 7 CFU / mL), 37°C 5% CO 2 Incubate for 48 h in the incubator. After the incubation, centrifuge at 1500 rpm for 10 min, aspirate the supernatant, filter with a 0.22 μm filter, and measure the IL-10 and IL-12 content by ELISA ki...
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