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*,
{"title":"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","authors":"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*, ","doi":"10.1021/acsptsci.5c00416","DOIUrl":null,"url":null,"abstract":"<p >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 <i>in vitro</i> and <i>in vivo</i> drug metabolism and pharmacokinetic profiling we selected <b>VU6032735</b> to utilize as a tool compound. <b>VU6032735</b> 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, <b>VU6032735</b> 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.</p>","PeriodicalId":36426,"journal":{"name":"ACS Pharmacology and Translational Science","volume":"8 9","pages":"3281–3295"},"PeriodicalIF":3.7000,"publicationDate":"2025-08-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://pubs.acs.org/doi/pdf/10.1021/acsptsci.5c00416","citationCount":"0","resultStr":"{\"title\":\"Highly Potent and Subtype-Selective Sperm-Specific Potassium Channel SLO3 Inhibitors Display High Tissue Exposure in the Murine Female Reproductive Tract\",\"authors\":\"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*, \",\"doi\":\"10.1021/acsptsci.5c00416\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >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 <i>in vitro</i> and <i>in vivo</i> drug metabolism and pharmacokinetic profiling we selected <b>VU6032735</b> to utilize as a tool compound. <b>VU6032735</b> 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, <b>VU6032735</b> 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.</p>\",\"PeriodicalId\":36426,\"journal\":{\"name\":\"ACS Pharmacology and Translational Science\",\"volume\":\"8 9\",\"pages\":\"3281–3295\"},\"PeriodicalIF\":3.7000,\"publicationDate\":\"2025-08-15\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://pubs.acs.org/doi/pdf/10.1021/acsptsci.5c00416\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ACS Pharmacology and Translational Science\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://pubs.acs.org/doi/10.1021/acsptsci.5c00416\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, MEDICINAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Pharmacology and Translational Science","FirstCategoryId":"1085","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acsptsci.5c00416","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MEDICINAL","Score":null,"Total":0}
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.
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.
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