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Quantification of Pelvic Organ Prolapse in Mice: Vaginal Protease Activity Precedes Increased MOPQ Scores in Fibulin 5 Knockout Mice1

机译:小鼠盆腔脏器脱垂的定量:阴道蛋白酶活性先于增加的Fibulin 5基因敲除小鼠MOPQ得分1

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摘要

Two mouse models of pelvic organ prolapse have been generated recently, both of which have null mutations in genes involved in elastic fiber synthesis and assembly (fibulin 5 and lysyl oxidase-like 1). Interestingly, although these mice exhibit elastinopathies early in life, pelvic organ prolapse does not develop until later in life. In this investigation we developed and validated a tool to quantify the severity of pelvic organ prolapse in mice, and we used this tool prospectively to study the role of fibulin 5, aging, and vaginal proteases in the development of pelvic organ prolapse. The results indicate that >90% of Fbln5−/− mice develop prolapse by 6 mo of age, even in the absence of vaginal delivery, and that increased vaginal protease activity precedes the development of prolapse.
机译:最近已经产生了两种小鼠盆腔器官脱垂的模型,它们都在涉及弹性纤维合成和组装的基因(血纤蛋白5和赖氨酰氧化酶样1)中没有无效突变。有趣的是,尽管这些小鼠在生命早期就表现出弹性病,但直到生命晚期才发展出盆腔器官脱垂。在这项研究中,我们开发并验证了一种量化小鼠骨盆器官脱垂严重程度的工具,并且前瞻性地使用了该工具来研究血纤蛋白5,衰老和阴道蛋白酶在骨盆器官脱垂发展中的作用。结果表明,即使在没有阴道分娩的情况下,超过90%的Fbln5-/-小鼠也会在6个月大时出现脱垂,并且阴道蛋白酶的活性增加会在脱垂发生之前。

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