Charles River Laboratories, Pathology Associates, Durham, North Carolina.
GlaxoSmithKline Research & Development, King of Prussia, Pennsylvania.
Birth Defects Res. 2018 Feb 15;110(3):190-227. doi: 10.1002/bdr2.1133. Epub 2017 Oct 24.
This review describes pre- and postnatal development of the male reproductive system in humans and laboratory animals, and highlights species differences in the timing and control of hormonal and morphologic events. Major differences are that the fetal testis is dependent on gonadotropins in humans, but is independent of such in rats; humans have an extended postnatal quiescent period, whereas rats exhibit no quiescence; and events such as secretion by the prostate and seminal vesicles, testicular descent, and the appearance of spermatogonia are all prenatal events in humans, but are postnatal events in rats. Major differences in the timing of the developmental sequence between rats and humans include: gonocyte transformation period (rat: postnatal day 0-9; human: includes gestational week 22 to 9 months of age); masculinization programming window (rat: gestational day 15.5-17.5; human: gestational week 9-14); and mini-puberty (rat: 0-6 hr after birth; human: 3-6 months of age). Endocrine disruptors can cause unique lesions in the prenatal and early postnatal testis; therefore, it is important to consider the differences in the timing of the developmental sequence when designing preclinical studies as identification of windows of sensitivity for endocrine disruption or toxicants will aid in interpretation of results and provide clues to a mode of action. Birth Defects Research 110:190-227, 2018. © 2017 Wiley Periodicals, Inc.
这篇综述描述了人类和实验动物雄性生殖系统的产前和产后发育,并强调了激素和形态事件的时间和控制方面的物种差异。主要差异在于,人类胎儿的睾丸依赖于促性腺激素,而老鼠的睾丸则不依赖于促性腺激素;人类有一个延长的产后静止期,而老鼠则没有静止期;前列腺和精囊的分泌、睾丸下降和精原细胞出现等事件在人类中都是产前事件,而在老鼠中则是产后事件。大鼠和人类之间发育序列时间的主要差异包括:精原细胞转化期(大鼠:出生后第 0-9 天;人类:包括妊娠第 22 周至 9 个月龄);雄性化编程窗口(大鼠:妊娠第 15.5-17.5 天;人类:妊娠第 9-14 周);和微小青春期(大鼠:出生后 0-6 小时;人类:3-6 个月龄)。内分泌干扰物会在产前和早期产后睾丸中引起独特的病变;因此,在设计临床前研究时,考虑到发育序列时间的差异非常重要,因为确定内分泌干扰或毒物的敏感窗口将有助于解释结果,并提供作用模式的线索。出生缺陷研究 110:190-227, 2018. © 2017 Wiley Periodicals, Inc.