Application of Intervention 14-3-3 in the Treatment of Sepsis
A sepsis, 1.BV02 technology, applied in the application field of intervention 14-3-3 in the treatment of sepsis, can solve the problems of lack of early effective drug treatment, unclear activation mechanism, high mortality, etc. To achieve the effect of slowing down the pathological damage of the lungs, slowing down the storm of inflammatory factors, and improving the survival rate
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Embodiment 114-3-3
[0021] Example 1 Study on 14-3-3 myeloid cell-deficient mice
[0022] Using 4-6 weeks of SPF grade female C57BL / 6 mice, WT mice and 14-3-3 gene-deficient mice were used to establish cecal ligation sepsis (CLP) models. Observe and record the mouse survival rate, the results are as follows: figure 1 As shown in A.
[0023] 4-6 weeks old SPF grade female C57BL / 6 mice were used to construct a mouse cecal ligation sepsis model (construct a cecal ligation sepsis model mouse according to the conventional method in the field). Take mouse lung and peritoneal lavage fluid. The lung lobules were fixed with 4% paraformaldehyde, the lung tissue sections were stained with H&E, and observed under a microscope, the results were as follows figure 1 Shown in B.
[0024] The remaining lung tissue was ground, filtered, and stained with specific flow cytometry antibodies together with peritoneal lavage fluid to detect antibodies CD11b+, F4 / 80+ and IL-1β respectively. The results are as follows...
Embodiment 2
[0029] Example 2 Effect of 14-3-3 Inhibitor BV02 on Sepsis Model Mice
[0030] Using 4-6 week SPF grade female C57BL / 6 mice, the tail vein was injected with the same amount of BV02 and DMSO (both 10mg / kg), and after 12 hours, the mouse cecal ligation sepsis model was constructed, and the small mice were observed and recorded. Rat survival, structured as figure 2 As shown in A.
[0031] 4-6 weeks old SPF grade female C57BL / 6 mice were used to inject the same amount of BV02 and DMSO (both 10mg / kg) into the tail vein. After 12 hours, a mouse cecal ligation sepsis model was constructed, and the mouse lungs and Peritoneal lavage fluid. The lung tissue was ground, filtered, and performed specific flow cytometry antibody staining together with peritoneal lavage fluid to detect antibodies CD11b+, F4 / 80+, and ly6G respectively + and IL-1β, the results were as figure 2 B. figure 2 C and figure 2 D shows.
[0032] figure 2 A The results showed that the survival rate of mice ...
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