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中文摘要
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这个子项目是许多研究子项目中的一个 由NIH/NCRR资助的中心赠款提供的资源。子项目和 研究者(PI)可能从另一个NIH来源获得了主要资金, 因此可以在其他CRISP条目中表示。所列机构为 研究中心,而研究中心不一定是研究者所在的机构。 俄勒冈州国家灵长类动物研究中心和俄勒冈州健康与科学大学建立了U 54避孕开发研究中心,旨在发现和开发新型避孕药物,防止一种或多种 成年雌性灵长类在月经周期中的排卵期事件。 三个研究项目和一个动物核心利用旧世界(猕猴)猴子产生新的信息和概念验证的方式,防止卵母细胞受精,从而生育,在妇女。 项目I,“卵母细胞成熟的控制”,将解决新的卵泡细胞和卵母细胞衍生的假设, 蛋白质控制卵母细胞的细胞核和细胞质成熟,并且可以用来破坏适时的卵成熟。 项目II,“控制排卵”,将分析卵泡/卵丘和卵母细胞衍生的蛋白质,控制卵丘卵母细胞扩张和卵泡破裂,并测试拮抗剂是否阻止排卵和卵子释放。 项目III,“配子运输和受精的控制”测试雌激素作用对正常输卵管和宫颈功能至关重要的假设,例如选择性雌激素受体调节剂(SERM)将破坏配子运输,从而破坏受精。 在项目I-III中发现的有希望的药物将在非人灵长类避孕药核心中进行避孕效力和可逆性测试。 与制药业和OB/GYN,OHSU的现有联系将促进与制定新型卵巢/生殖道避孕药相关的转化研究。请参阅各个项目的进度报告和出版物。
英文摘要
This subproject is one of many research subprojects utilizing the resources provided by a Center grant funded by NIH/NCRR. The subproject and investigator (PI) may have received primary funding from another NIH source, and thus could be represented in other CRISP entries. The institution listed is for the Center, which is not necessarily the institution for the investigator. The Oregon National Primate Research Center and the Oregon Health & Science University established a U54 Contraceptive Development Research Center that targets the discovery and development of novel contraceptive drugs that prevent one or more periovulatory events in adult, female primates during the menstrual cycle. Three research projects and one animal core utilize Old World (macaque) monkeys to generate new information and proof-of-concept regarding modalities that prevent oocyte fertilization, and hence fertility, in women. Project I, "Control of Oocyte Maturation", will address the hypothesis that novel follicle cell-, and oocyte-derived proteins control nuclear and cytoplasmic maturation of the oocyte, and can be exploited to disrupt timely egg maturation. Project II, "Control of Ovulation", will analyze follicle/cumulus- and oocyte-derived proteins that control cumulus-oocyte expansion and follicle rupture, and test whether antagonists prevent ovulation and egg release. Project III, "Control of Gamete Transport and Fertilization" tests the hypothesis that estrogen action is essential for normal oviductal and cervical function, such that a selective estrogen receptor modulator (SERM) will disrupt gamete transport, and hence, fertilization. Promising agents discovered in Projects I - III will be tested in the Nonhuman Primate Contraceptive Core for contraceptive efficacy and reversibility. Existing ties with the pharmaceutical industry and OB/GYN, OHSU, will promote translational research relevant to formulating novel ovary/reproductive tract-based contraceptives for women. See individual projects for progress reports and publications.
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Hyperandrogenemia, Diet and Female Reproductive Health
PROJECT 2: OVARIAN AND UTERINE RESPONSES TO ANDROGEN AND DIET
Hyperandrogenemia, Diet and Female Reproductive Health
Hyperandrogenemia, Diet and Female Reproductive Health
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