Culture solution, and method for improving quality of maternal diabetic ova
A culture medium and diabetes technology, applied in the field of reproductive biology, can solve the problems of reduced egg fertilization rate, reduced embryonic development potential, high disease risk, etc., and achieve the effect of improving fertility problems, no toxic side effects, and improving egg quality.
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Embodiment 1
[0053] Embodiment 1 culture fluid
[0054] The culture medium includes the following components: tea polyphenols (50 μM), heat-inactivated fetal bovine serum (volume fraction 5%), sodium pyruvate (0.25 mM), 100× penicillin and streptomycin (volume fraction 0.75%), FSH (0.5 U / ml) and α-MEM medium.
Embodiment 2
[0055] Embodiment 2 culture fluid
[0056] Except that the concentration of tea polyphenols is 25 μM, other formulations and concentrations are the same as in Example 1.
Embodiment 3
[0057] Embodiment 3 The method for improving maternal diabetes egg quality
[0058] (1) Constructing a maternal diabetic animal model, and isolating the cumulus-oocyte complex from the maternal diabetic animal model: The maternal diabetic animal model was established by intraperitoneal injection of 220 mg / kg body weight of STZ. First select the body weight of 7-8 week old mice, and determine the amount of STZ. Dissolve STZ with citric acid-sodium citrate buffer on ice in the dark, and inject no more than 100 microliters per mouse. After 4 days, blood was taken from the tip of the tail, and the blood glucose concentration was measured with a blood glucose meter. If it was greater than or equal to 17.0 mM / L, the model was considered successful. 10 days after successful model construction, intraperitoneal injection of PMSG 8IU, ovaries were collected 46-48 hours later, the follicles were punctured with a 1ml syringe needle under a dissecting microscope, and COCs were collected. ...
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