Application of MPLA in the preparation of drugs for prevention and treatment of testicular injury induced by ionizing radiation
An ionizing radiation, testicular technology, applied in the field of medicine, can solve problems such as testicular damage, achieve the effects of less toxic and side effects, increase sperm motility and sperm count, and reduce the degree of necrosis
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Embodiment 1
[0036] Firstly, a mouse model of radiation-induced testicular injury was established, and 18 male C57BL / 6 mice aged 6-8 weeks were selected and randomly divided into 3 groups, 6 mice in each group: 3 mice in the irradiation group (4Gy) and 12 hours before irradiation with MPLA. 3 rats in the drug group (4Gy+MPLA) and 3 rats in the control group; 60 Coγ-rays were irradiated to the abdomen of the mice once, and the absorbed dose of the mice was 4Gy. MPLA (administration dose 50 μg / kg, MPLA dissolved in 0.1 ml physiological saline) or physiological saline (0.1 ml / mouse) were delivered to the corresponding groups by intragastric administration. On the first day and the seventh day after radiation exposure, the testes of 8 mice in each group were taken respectively, fixed, embedded in wax blocks, and sectioned for HE staining (such as figure 1 shown). Observation under the microscope showed that the structure of the testis in the non-irradiated group was complete, the cells were ...
Embodiment 2
[0038] (1) The radiation-induced testicular injury mouse model is the same as that in Example 1;
[0039] (2) Male TLR4 knockout mice aged 6-8 weeks were selected and randomly divided into 3 groups, 3 mice in each group: the simple irradiation group and the control group were intragastrically administered with normal saline (0.1ml / mouse) 12 hours before irradiation, The irradiation administration group was administrated with MPLA 12 hours before irradiation (administration dose was 50 μg / kg, MPLA was dissolved in 0.1ml normal saline), and the mice were killed on the seventh day after irradiation, and the testis tissues were taken, fixed, embedded in wax blocks, and sectioned. followed by HE staining (e.g. figure 2 Shown), under the microscope, it was found that the structure of the testis in the non-irradiated group was complete, the cells were large, the seminiferous tubules were full, and the outline was clear, which was not significantly different from that of the wild-typ...
Embodiment 3
[0041] (1) The radiation-induced testicular injury mouse model is the same as that in Example 1;
[0042] (2) Select 6 male C57BL / 6 mice aged 6-8 weeks, and randomly divide them into 2 groups, 3 mice in each group. The administration group was administrated with MPLA 12 hours before irradiation (administration dose was 50 μg / kg, MPLA was dissolved in 0.1ml normal saline), and the mice were killed 16 hours after irradiation, and the testis tissues were taken, fixed, embedded in wax blocks, sliced, Carry out TUNEL (terminal dexynucleotidyl transferase (TdT)-mediateddUTP nick end labeling, terminal deoxynucleotidyl transferase-mediated dUTP nick end labeling assay) staining, observe under a microscope, and randomly select 10 low-magnification fields of view for TUNEL-positive cells Count and calculate the average (such as image 3 As shown), the results showed that the testicular TUNEL positive cells in the simple irradiation group were significantly more than those in the irrad...
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