Florey Neuroscience Institutes, University of Melbourne, Parkville, Melbourne, Victoria 3010, Australia.
Peptides. 2009 Oct;30(10):1861-5. doi: 10.1016/j.peptides.2009.07.019. Epub 2009 Aug 6.
During human pregnancy, a circulating form of insulin-regulated aminopeptidase (IRAP EC 3.4.11.3), often termed oxytocinase or placental leucine aminopeptidase (PLAP), is present in plasma. It is proposed that circulating IRAP plays an important role in regulating the circulating levels of oxytocin and/or vasopressin during pregnancy. We assessed the reproductive and maternal profile of global IRAP knock out mice. No differences in the reproductive profile were observed, with normal gestational period, litter size and parturition recorded. However, western blot analysis of pregnant mouse serum, failed to detect IRAP, a result which was confirmed by fluorimetric IRAP enzyme assay. A review of the literature revealed that the presence of IRAP in the maternal circulation during pregnancy has been only reported in humans. Moreover, the sequence, Phe154 Ala155, identified as the cleavage site for the release of soluble IRAP, is restricted to members of the homindae family. Therefore the absence of IRAP from the circulation in mice, and other species during pregnancy, is due to the inability of a secretase to cleave placental IRAP to produce a soluble form of the enzyme. Given the expression of IRAP in areas of the brain associated with oxytocin modulated maternal behavior, we also investigated whether the IRAP global knockout mice had improved maternal responses. Using standard tests to assess maternal behavior, including pup retrieval, feeding and nurturing, no differences between knock out and wild type dams were observed. In conclusion, the physiological significance of circulating IRAP during human pregnancy cannot be addressed by investigations on mice.
在人类妊娠期间,循环形式的胰岛素调节氨肽酶(IRAP EC 3.4.11.3),通常称为催产素酶或胎盘亮氨酸氨肽酶(PLAP),存在于血浆中。据推测,循环中的 IRAP 在调节妊娠期间催产素和/或加压素的循环水平方面发挥重要作用。我们评估了全球 IRAP 敲除小鼠的生殖和母性特征。没有观察到生殖特征的差异,记录了正常的妊娠期、产仔数和分娩。然而,对怀孕小鼠血清的 Western blot 分析未能检测到 IRAP,这一结果通过荧光 IRAP 酶测定得到了证实。对文献的回顾表明,IRAP 存在于妊娠期间的母体循环中仅在人类中报道过。此外,作为释放可溶性 IRAP 的切割位点鉴定的 Phe154 Ala155 序列仅限于同源家族的成员。因此,IRAP 在怀孕小鼠和其他物种的循环中缺失是由于缺乏一种能切割胎盘 IRAP 以产生该酶可溶性形式的蛋白酶。鉴于 IRAP 在与催产素调节母性行为相关的大脑区域表达,我们还研究了 IRAP 全局敲除小鼠是否具有改善的母性行为反应。使用评估母性行为的标准测试,包括幼仔回收、喂养和养育,未观察到敲除和野生型母鼠之间的差异。总之,不能通过对小鼠的研究来解决人类妊娠期间循环中的 IRAP 的生理意义。