Ruetten Hannah, Wegner Kyle A, Zhang Helen L, Wang Peiqing, Sandhu Jaskiran, Sandhu Simran, Morkrid Jacquelyn, Mueller Brett, Wang Zunyi, Macoska Jill, Peterson Richard E, Bjorling Dale E, Ricke William A, Marker Paul C, Vezina Chad M
Department of Comparative Biosciences, University of Wisconsin-Madison, WI, USA.
University of Wisconsin-Madison/UMASS Boston George M. O'Brien Center for Benign Urologic Research, Madison, WI, and Boston, MA, USA.
Toxicol Pathol. 2019 Dec;47(8):1038-1042. doi: 10.1177/0192623319877867. Epub 2019 Oct 29.
The purpose of this symposium report is to summarize information from a session 3 oral presentation at the Society of Toxicologic Pathology Annual Symposium in Raleigh, North Carolina. Mice are genetically tractable and are likely to play an important role in elucidating environmental, genetic, and aging-related mechanisms of urinary dysfunction in men. We and others have made significant strides in developing quantitative methods for assessing mouse urinary function and our collaborators recently showed that aging male mice, like men, develop urinary dysfunction. Yet, it remains unclear how mouse prostate anatomy and histology relate to urinary function. The purpose of this report is to share foundational resources for evaluating mouse prostate histology and urinary physiology from our recent publication "Impact of Sex, Androgens, and Prostate Size on C57BL/6J Mouse Urinary Physiology: Functional Assessment." We will begin with a review of prostatic embryology in men and mice, then move to comparative histology resources, and conclude with quantitative measures of rodent urinary physiology.
本专题研讨会报告的目的是总结在北卡罗来纳州罗利市举行的毒理病理学会年度研讨会上一场口头报告的信息。小鼠具有遗传易处理性,在阐明男性泌尿系统功能障碍的环境、遗传和衰老相关机制方面可能发挥重要作用。我们和其他研究人员在开发评估小鼠泌尿系统功能的定量方法方面取得了重大进展,我们的合作者最近发现,衰老的雄性小鼠与男性一样,会出现泌尿系统功能障碍。然而,小鼠前列腺的解剖结构和组织学与泌尿系统功能之间的关系仍不清楚。本报告的目的是分享我们最近发表的《性别、雄激素和前列腺大小对C57BL/6J小鼠泌尿系统生理学的影响:功能评估》中评估小鼠前列腺组织学和泌尿系统生理学的基础资源。我们将首先回顾人类和小鼠前列腺的胚胎学,然后转向比较组织学资源,最后以啮齿动物泌尿系统生理学的定量测量作为总结。