高效和亚型选择性精子特异性钾通道SLO3抑制剂在小鼠雌性生殖道中显示高组织暴露

IF 3.7 Q1 CHEMISTRY, MEDICINAL
Kayla J. Temple*, Ping Li, Hallie G. McKinnie, Analisa Thompson Gray, Jeanette L. Bertron, Anna E. Ringuette, Pedro de Andrade Horn, Maximilian D. Lyon, Shweta Bhagwat, Leila Asadi, Sophia Li, Roman M. Lazarenko, Ronald McCarthy, Sichen Chang, Jeremy A. Turkett, Valerie Kramlinger, Katherine J. Watson, Irene A. Zagol-Ikapitte, Jerod S. Denton, Celia M. Santi, Carrie K. Jones, Craig W. Lindsley and Olivier Boutaud*, 
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引用次数: 0

摘要

迄今为止,药物暴露和分布在整个女性生殖道的研究往往被忽视和忽视。在这里,我们报道了第一个高效和亚型选择性精子特异性钾通道3 (SLO3)抑制剂作为一种新的避孕方式。经过广泛的体外和体内药物代谢和药代动力学分析,我们选择了VU6032735作为工具化合物。VU6032735清除率低,半衰期长,在雌性小鼠中分布大,似乎是非激素避孕药的理想靶点。在腹腔注射后,我们评估了药物在小鼠雌性生殖道各腔室的暴露和分布。在24小时的时间过程中,VU6032735在输卵管中保持高组织暴露,输卵管是受精发生的地方。这项工作为其他对研究女性生殖道药物暴露和分布感兴趣的人提供了框架。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Highly Potent and Subtype-Selective Sperm-Specific Potassium Channel SLO3 Inhibitors Display High Tissue Exposure in the Murine Female Reproductive Tract

To date, the study of drug exposure and distribution throughout the female reproductive tract has often been overlooked and neglected. Herein, we report the first highly potent and subtype-selective sperm-specific potassium channel 3 (SLO3) inhibitors as a new modality of contraceptives. After extensive in vitro and in vivo drug metabolism and pharmacokinetic profiling we selected VU6032735 to utilize as a tool compound. VU6032735 displayed low observed clearance with a long half-life and a high volume of distribution in female mice, which is seemingly an ideal target profile for a nonhormonal contraceptive. After intraperitoneal injection, we evaluated the drug exposure and distribution throughout various compartments of the murine female reproductive tract. Over a 24-h time course, VU6032735 sustained high tissue exposure in the oviduct, where fertilization takes place. This work provides the framework for others interested in studying drug exposure and distribution throughout the female reproductive tract.

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来源期刊
ACS Pharmacology and Translational Science
ACS Pharmacology and Translational Science Medicine-Pharmacology (medical)
CiteScore
10.00
自引率
3.30%
发文量
133
期刊介绍: ACS Pharmacology & Translational Science publishes high quality, innovative, and impactful research across the broad spectrum of biological sciences, covering basic and molecular sciences through to translational preclinical studies. Clinical studies that address novel mechanisms of action, and methodological papers that provide innovation, and advance translation, will also be considered. We give priority to studies that fully integrate basic pharmacological and/or biochemical findings into physiological processes that have translational potential in a broad range of biomedical disciplines. Therefore, studies that employ a complementary blend of in vitro and in vivo systems are of particular interest to the journal. Nonetheless, all innovative and impactful research that has an articulated translational relevance will be considered. ACS Pharmacology & Translational Science does not publish research on biological extracts that have unknown concentration or unknown chemical composition. Authors are encouraged to use the pre-submission inquiry mechanism to ensure relevance and appropriateness of research.
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