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非典型胎儿前列腺发育与 ACI 大鼠同侧沃尔夫管发育不良有关。

Atypical fetal prostate development is associated with ipsilateral hypoplasia of the wolffian ducts in the ACI rat.

机构信息

Division of Basic Biomedical Sciences, Sanford School of Medicine, Lee Medical Building, University of South Dakota, Vermillion, South Dakota, USA.

出版信息

Anat Rec (Hoboken). 2010 May;293(5):747-53. doi: 10.1002/ar.21073.

Abstract

For over a half century, the ACI (August x Copenhagen) rat has been a primary model for studying renal agenesis and ipsilateral hypoplasia (IHP) of the Wolffian-derived structures (WDS). Because the ACI rat is also used as a model for prostate research, it is important to examine the relationship of IHP and urogenital sinus (UGS) development. The prostate is dependent on androgens for proper growth and differentiation. Alteration in androgen production and/or delivery to the UGS has the potential to perturbate normal development. In this study, we investigate whether the ipsilateral loss of the WDS is associated with altered prostate development. Digital images of serial-sectioned fetal ACI rat UGS were used to create three-dimensional (3-D) surface-rendered models of the developing prostate, seminal vesicle, vas deferens, and utricle on gestational day 21. The number and volume of prostate ducts developing from the UGS were calculated from the 3-D model data. Animals exhibiting IHP had a significant decrease in total fetal prostate volume (40%; P < 0.005) with significant regional specific differences when compared with normal male ACI rats. Anatomical and histological differences in the utricle, abnormal histology of the ipsilateral testes, and a truncation of the ipsilateral Wolffian ductal mesenchyme were also seen in the animals with IHP. Additional research is needed to further understand the mechanisms and consequences of IHP on prostate growth and development. Alterations to normal prenatal development of the male accessory sex organs can have important consequences for the growth and morphology of the adult gland.

摘要

半个多世纪以来,ACI(八月 x 哥本哈根)大鼠一直是研究肾发育不全和同侧沃尔夫氏管衍化结构(WDS)发育不良(IHP)的主要模型。由于 ACI 大鼠也被用作前列腺研究的模型,因此检查 IHP 和尿生殖窦(UGS)发育之间的关系非常重要。前列腺的正常生长和分化依赖于雄激素。雄激素的产生和/或向 UGS 的输送的改变有可能扰乱正常发育。在这项研究中,我们研究了同侧 WDS 的缺失是否与前列腺发育异常有关。对 ACI 大鼠 UGS 的连续切片进行数字成像,用于在妊娠第 21 天创建发育中的前列腺、精囊、输精管和输囊管的三维(3-D)表面渲染模型。从 3-D 模型数据计算出从 UGS 发育而来的前列腺导管的数量和体积。与正常雄性 ACI 大鼠相比,表现出 IHP 的动物的总胎儿前列腺体积显著减少(40%;P < 0.005),并且具有显著的区域特异性差异。在患有 IHP 的动物中还观察到了输囊管的解剖和组织学差异、同侧睾丸的异常组织学以及同侧沃尔夫氏管导管间充质的截断。需要进一步研究以进一步了解 IHP 对前列腺生长和发育的机制和后果。对男性附属生殖器官正常产前发育的改变可能对成年腺体的生长和形态产生重要影响。

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