Application of GPR1 (G protein coupled receptor 1) target and its antagonist in infertility-related diseases
An antagonist and disease technology, which is applied in the application field of GPR1 and its antagonists in the treatment of ovulation disorder-related diseases, and can solve the problems of not protecting patients with premature ovarian failure, etc.
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Embodiment 1
[0046] Example 1. Interfering with the gene expression of GPR1, or antagonizing the function of GPR1, can effectively alleviate the symptoms of polycystic ovary syndrome in experimental mice caused by DHEA.
[0047] In this example, it is verified that interfering with the gene expression of GPR1, or antagonizing the effect of GPR1, can effectively alleviate the symptoms of experimental mouse polycystic ovary syndrome caused by DHEA. Among them, an experimental mouse polycystic ovary syndrome model induced by hyperandrogen DHEA was established. However, compared with wild-type mice, the symptoms of polycystic ovary syndrome in GPR1 knockout mice were significantly alleviated, including: increased serum estrogen levels, and corpus luteum production on the ovaries.
[0048] details as follows:
[0049] (1) DHEA experimental mouse polycystic ovary syndrome model
[0050] GPR1 knockout mice in C57BL / 6J background were purchased from Deltagen Co., Ltd. and provided by Dr. ZABLE's...
Embodiment 2
[0066] Example 2: GPR1 regulates the expression of estrogen-related synthetase caused by DHEA through the mTOR signaling pathway
[0067] C57BL / 6J wild-type female mice were from Guangdong Medical Experimental Animal Center.
[0068] Animals were housed in a vivarium with a 12-h light-dark cycle at constant temperature and humidity. Feed and water were available ad libitum. All animal procedures were performed in accordance with procedures approved by the Animal Welfare Ethics Committee.
[0069] The mice were intraperitoneally injected with 5IU PMSG (pregnant horse serum gonadotropin) at 21 days, and then 5IU hCG (human chorionic gonadotropin) was injected intraperitoneally after 48 hours. After 7-12 hours, the mice were killed, the ovaries were removed, and the follicles were punctured. Pass through a 70um sieve three times to remove oocytes, centrifuge at 1000g for 5 minutes, discard the supernatant, and resuspend in a serum-free DMEM F12+3%BSA+ITS incubator at 37°C, 5%CO...
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