Klein K L, Scott W J, Clark K E, Wilson J G
Am J Obstet Gynecol. 1981 Oct 15;141(4):448-52. doi: 10.1016/0002-9378(81)90610-4.
Aspirin is a well-known teratogen in laboratory animals and is an inhibitor of prostaglandin synthesis. To further investigate the inhibition of prostaglandin synthesis as a mechanism of teratogenesis, we examined the teratologic potential, cytotoxic potential, and placental transfer of indomethacin in the rat. Indomethacin was not teratologic, not cytotoxic to cells in the embryonic hindlimb bud, and did not cross the placenta in physiologically significant amounts on days 11 to 12 of gestation. Near parturition, however, indomethacin crossed the placenta in pharmacologically significant amounts. The pharmacokinetics of placental drug transfer are discussed.
阿司匹林在实验动物中是一种众所周知的致畸剂,并且是前列腺素合成的抑制剂。为了进一步研究前列腺素合成抑制作为致畸机制,我们检测了吲哚美辛在大鼠中的致畸潜力、细胞毒性潜力以及胎盘转运情况。吲哚美辛没有致畸性,对胚胎后肢芽中的细胞没有细胞毒性,并且在妊娠第11至12天不会以具有生理意义的量穿过胎盘。然而,在临近分娩时,吲哚美辛会以具有药理意义的量穿过胎盘。本文讨论了胎盘药物转运的药代动力学。