Bifidobacterium bifidum M2017063 and application thereof in preparation of drugs for relieving symptoms of chronic renal diseases
A technology of Bifidobacterium bifidum and strains, applied in the field of microbiology, can solve the problems of unsatisfactory effect and high cost of kidney transplantation, and achieve the effect of strong ability to remove creatinine and urea nitrogen, high research value and application value
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Embodiment 1
[0022] Example 1: Isolation and identification of Bifidobacterium bifidum CCTCC M2017063
[0023] Bifidobacterium bifidum CCTCC M2017063 was isolated from feces of healthy young children. Dissolve 1g of feces in 10mL of 10% peptone solution, stir and dissolve the glass rod fully, filter out the residue with filter paper, collect the filtrate and centrifuge at 5000rmp for 10min, discard the supernatant, and resuspend the precipitate with 1mL of 10% peptone water. Inoculate 1% into the liquid medium of MRS+0.5% L-cysteine, and culture overnight at 37°C anaerobically. The culture solution was serially diluted 10 times, and 10 -4 、10 -5 、10 -6 、10 -7 1 mL of the gradient dilution solution was evenly spread on the agar plate of MRS+0.5% L-cysteine, and cultured anaerobically at 37°C for 48h. Pick a single colony, separate it by streaking on the plate, carry out repeated purification and culture, observe the colony morphology with Gram staining method to select Gram-positive ba...
Embodiment 2
[0026] Embodiment 2: the effect of bacterial strain on adenine-induced chronic kidney injury mice
[0027] 30 female Balb / C mice were randomly divided into three groups, normal group (10): intragastric administration of 100 μl of normal saline; model group (10): intragastric administration of 100 μl of 2% adenine suspension every day, a total of 4 week. Bifidobacterium bifidum CCTCC M 2017063 group (10 rats): after intragastric administration of 100 μl of 2% adenine suspension daily for 1 week, resuspend Bifidobacterium bifidum CCTCC M 2017063 in 2% adenine suspension daily Suspension, respectively, 100μl orally for 3 weeks. After feeding, blood was collected from the eye sockets, and the mice were sacrificed by neck dislocation. After the plasma was allowed to stand at 4°C, the serum was collected to detect relevant biochemical indicators. The kidneys were taken for HE staining, and the degree of renal failure and improvement of the mice were observed.
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