Control of Oocyte Maturation

卵母细胞成熟的控制

• 批准号: 8538480
• 负责人: JEFFREY T. JENSEN
• 金额: $ 32.72万
• 依托单位: OREGON HEALTH & SCIENCE UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2007
• 资助国家: 美国
• 起止时间: 2007-03-31 至
• 项目状态: 未结题
• 来源: https://reporter.nih.gov/project-details/8538480
• 关键词: Adverse effects; Affect; Agonist; Biological Availability; Cell Cycle; Cells; Clinical Trials; Collaborations; Contraceptive Agents; Contraceptive Usage; Contraceptive methods; Controlled Study; Couples; Cyclic AMP; Cyclic GMP; Data; Development; Dose; Drug Delivery Systems; Drug Kinetics; Drug Targeting; Enzymes; Event; Experimental Designs; Family member; Female; Female Contraceptive Agents; Fertilization; Fertilization in Vitro; Gap Junctions; Gene Expression; Generations; Germ Cells; Goals; Hormonal; Housing; Implant; In Vitro; Instruction; Intracytoplasmic Sperm Injections; Luteinizing Hormone; Macaca; Macaca mulatta; Maintenance; Maturation-Promoting Factor; Meiosis; Menstrual cycle; Metabolism; Metaphase; Methods; Minnesota; Mitosis; Mitotic; Modeling; Molecular; Monitor; Nuclear; Oocytes; Oral; Ovulation; PDE3A gene product; Partner in relationship; Pathway interactions; Periodicity; Pharmaceutical Chemistry; Pharmaceutical Preparations; Pharmacodynamics; Phosphodiesterase Inhibitors; Phosphotransferases; Play; Pregnancy; Primates; Protein Kinase; Research; Rest; Rodent; Role; Safety; Source; System; Testing; Toxic effect; Universities; Unwanted Birth; Vaginal Ring; Vesicle; Woman; abortion; base; design; drug candidate; granulosa cell; high throughput screening; improved; in vitro activity; in vivo; inhibitor/antagonist; meetings; nonhuman primate; novel; oocyte maturation; phosphoric diester hydrolase; prevent; research study; unintended pregnancy

PROJECT SUMMARY (See instructions): The overall purpose of this research is to develop a gamete-based, nonhormonal female contraceptive. The most practical approach to an oocyte-specific nonhormonal contraceptive involves targeting of the phosphodiesterase (PDE)-regulated metabolism of cyclic adenosine monophosphate (cAMP) [a central controller of meiotic resumption upstream of M-phase Promoting Factor (MPF)], or direct targeting of activators or inhibitors of MPF. The principal regulator of cAMP in the follicle is PDE3. Cyclic guanosine monophosphate (cGMP) [produced in cumulus granulosa cells of the follicle, and transported to the oocyte via gap junctions] is an endogenous inhibitor of PDE3. PDE5 is the principal cGMP-degrading enzyme in follicle cells, and PDE9 is the only cGMP-degrading enzyme in the oocyte. The oocyte-specific protein kinase WEE2 is an essential regulator of MPF necessary for resumption of meiosis and for exit from metaphase II following fertilization. Our research plan is to develop and test inhibitors of these targets in nonhuman primates and to ultimately perform a contraceptive trial in macaques. The Specific Aims are: (1) To develop novel PDE and WEE2 inhibitors and determine if selected agents can disrupt timely meiotic maturation of the macaque oocyte; (2) To evaluate the pharmacoklnetics and pharmacodynamics of existing and novel PDE inhibitors and WEE2 inhibitors; and (3) To determine whether PDE and WEE2 inhibitors can function as contraceptive agents in regularly cycling macaques in group-mating situations. Experimental designs will include characterization of drug-target interactions, rational inhibitor design, high throughput screening and medicinal chemistry (Aim 1); testing of candidate agents for activity in vitro using incubation, in vitro fertilization, and intracytoplasmic sperm injection of macaque oocytes (Aim 1); Assessment of pharmacokinetic and phamacodynamic effects of candidate inhibitors in macaques in vivo with optimization of drug delivery (e.g. oral, vaginal ring, implant) systems and monitoring of non-target effects (Aim 2); and then conducting a contraceptive experiment in socially-housed female macaques (Aim 3). This approach is expected to establish the potential for PDE and WEE2 inhibitors as contraceptive agents for women.

项目总结（见说明）： 本研究的总体目的是开发一种基于配子的非激素女性避孕药。卵母细胞特异性非激素避孕的最实用方法涉及靶向磷酸二酯酶（PDE）调节的环磷酸腺苷（cAMP）代谢[M期促进因子（MPF）上游减数分裂恢复的中央控制器]，或直接靶向MPF的激活剂或抑制剂。卵泡中cAMP的主要调节因子是PDE 3。环磷酸鸟苷（cGMP）[在卵泡的卵丘颗粒细胞中产生，并通过间隙连接转运到卵母细胞]是PDE 3的内源性抑制剂。PDE 5是卵泡细胞中的主要cGMP降解酶，而PDE 9是卵母细胞中唯一的cGMP降解酶。卵母细胞特异性蛋白激酶WEE 2是MPF的重要调节因子，其对于减数分裂的恢复和退出是必需的。 受精后的中期II。我们的研究计划是在非人类灵长类动物中开发和测试这些靶点的抑制剂，并最终在猕猴中进行避孕试验。具体目标是：（1）开发新的PDE和WEE 2抑制剂，并确定所选择的药剂是否可以破坏猕猴卵母细胞的适时减数分裂成熟;（2）评估现有的PDE和WEE 2抑制剂的生物学和药效学。 和新的PDE抑制剂和WEE 2抑制剂;和（3）确定PDE和WEE 2抑制剂是否可以在组交配情况下在规律性周期性猕猴中作为避孕剂起作用。实验设计将包括药物-靶标相互作用的表征、合理的抑制剂设计、高通量筛选和药物化学（目标1）;使用孵育、体外受精和猕猴卵母细胞的胞浆内精子注射测试候选药物的体外活性（目标1）;候选抑制剂在猕猴体内的药代动力学和药效学效应的评估与药物递送的优化（例如口服、阴道环、植入物）系统和监测非目标效应（目标2）;然后在群居雌性猕猴中进行避孕实验（目标3）。这种方法 预计将确立PDE和WEE 2抑制剂作为女性避孕药的潜力。