Garg S K, Chaudhury R R
Arch Int Pharmacodyn Ther. 1983 Apr;262(2):299-307.
Indomethacin (IM), a potent inhibitor of prostaglandin synthetase, significantly inhibited implantation in rats when administered at a single subcutaneous dose of 15 mg/kg on day 2 or 3 of pregnancy or at a dose of 800 micrograms administered intraluminally in the uterus on day 4 of pregnancy. Indomethacin, administered subcutaneously at a dose of 6 mg/kg on day 3 or 4 of pregnancy and intraluminally at a dose of 800 micrograms/rat on day 4 of pregnancy, also significantly reduced uterine prostaglandin levels. It is suggested that a certain level of uterine prostaglandins is essential for normal implantation and that indomethacin inhibits implantation by reducing uterine prostaglandin levels.
吲哚美辛(IM)是一种强效的前列腺素合成酶抑制剂,在妊娠第2天或第3天以15毫克/千克的单次皮下剂量给药,或在妊娠第4天以800微克的剂量子宫腔内给药时,可显著抑制大鼠的着床。在妊娠第3天或第4天以6毫克/千克的皮下剂量给药,以及在妊娠第4天以800微克/大鼠的子宫腔内剂量给药的吲哚美辛,也显著降低了子宫前列腺素水平。提示一定水平的子宫前列腺素对正常着床至关重要,吲哚美辛通过降低子宫前列腺素水平来抑制着床。