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中文摘要
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摘要/摘要 哺乳动物的精子在通过卵母细胞时获得受精能力。 生殖道的一个被称为获能的过程。在获能过程中,精子 改变它们的运动模式,变得有能力经历顶体 反应并使卵母细胞受精这些与能力建设相关的进程需要 能量,精子依赖于环境中的营养物质来完成 他们精子在通过时会接触到周围环境中不同的营养物质 从储存在附睾尾到输卵管, 使卵母细胞受精在上一个融资期,我们证明, 外源性葡萄糖供精通过糖酵解和氧化作用产生ATP 磷酸化,并且通过这两种途径的葡萄糖利用增加, 使精子获能此外,我们发现,获能精子改变活动, 通过戊糖磷酸途径和精子剥夺外源性 营养素可以代谢内源能量来源。我们现在建议 现代代谢物分析与代谢通量分析相结合, 精子协调地调节它们的代谢途径, 外源营养素,因为它们通过不同的激活状态成熟。可溶性 腺苷酸环化酶(sAC)是必不可少的分子变化观察期间 能力,我们将使用我们独特的工具来调节其活动,以测试 假设sAC调节获能诱导的代谢变化。
英文摘要
Summary/Abstract Mammalian sperm acquire fertilization capacity as they transit through the reproductive tract in a process known as capacitation. During capacitation, sperm change their motility pattern and become competent to undergo an acrosome reaction and fertilize an oocyte. These capacitation-associated processes require energy, and sperm are dependent on nutrients in their environment to complete them. Sperm are exposed to different nutrients in their surroundings as they pass from being stored in the cauda epididymis to the fallopian tube where they will meet and fertilize the oocyte. In the previous funding period, we demonstrated that sperm supplied with exogenous glucose generate ATP via glycolysis and oxidative phosphorylation, and glucose utilization via both pathways increases in capacitating sperm. In addition, we found that capacitating sperm alter activity through the pentose phosphate pathway and sperm deprived of exogenous nutrients can metabolize endogenous energy sources. We now propose to apply modern metabolite profiling combined with metabolic flux analyses to identify how sperm coordinately regulate their metabolic pathways and leverage different exogenous nutrients as they mature through distinct activation states. Soluble adenylyl cyclase (sAC) is essential for the molecular changes observed during capacitation, and we will use our unique tools for modulating its activity to test the hypothesis that sAC regulates the metabolic changes induced by capacitation.
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Assessing inhibitor efficacy in vivo and developing a biomarker for use during early phase clinical trials
On-demand nonhormonal male contraception via ADCY10 inhibition
Development of new ADCY10 inhibitors
Optimization of lead candidates for an on-demand male contraceptive
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