Use of mpges-2 as a target in the development or screening or preparation of drugs for the prevention and/or treatment of diseases of aging
An aging and drug technology, applied in the field of biomedicine, can solve the problem of unclear mechanism of mPGES-2 regulating aging, and achieve the effects of improving exercise ability, promoting proliferation and cell rejuvenation
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Embodiment 1
[0045] Example 1 Doxorubicin-induced aging mouse model
[0046] MPGES-2 WT and KO mice were selected and divided into cages, and the day of the scoring cage was D0. On D1 and D7, intraperitoneal injection of doxorubicin 10 mg / kg body weight was performed to construct an aging model, and the body weight on the day was recorded. D8 is for rotarod fatigue meter adaptation, and D10 is for measurement.
Embodiment 2
[0047] Example 2 Rota-Rod:
[0048] The motor coordination ability of the mice was evaluated by a rotarod fatigue apparatus. The mouse was placed on the roller of the rotarod fatigue apparatus, and its tail was gently pulled to adjust to the rotarod, maintaining a balance movement. After three days of acclimatization, take the test. Rotor speed setting: 30r / min, acceleration from 1r / min to 30r / min, acceleration time 150s, test time 5min. Three rounds of testing were performed, and the average value was taken, with an interval of 10 min between each test. The mouse drop time was recorded.
Embodiment 3
[0049] Example 3 Isolation and culture of MEF cells:
[0050] The 13.5-day pregnant female mice were sacrificed by cervical dislocation, the abdomen was sterilized with alcohol, the abdominal cavity and uterus were opened aseptically, placed in a plate (PBS was added in advance), the fetal membranes were removed, and the fetus was removed (washed with PBS 3-4 times to remove blood cells)
[0051] The limbs, head, tail and internal organs of mouse embryos were removed with ophthalmic scissors, and washed 2-3 times with PBS. After rinsing, use ophthalmic scissors to cut into small tissue pieces of 1 mm.
[0052] For cell digestion and culture, add 4ml of 0.25% trypsin-EDTA, place at 37°C for digestion for 10-15min, and repeatedly pipet with a gun at 5min intervals until no obvious tissue blocks are visible. Digestion was terminated by adding an equal volume of DMEM (10% FBS). Transfer the cell suspension into a centrifuge tube, centrifuge at 1000 rpm for 5 min, and remove the ...
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