Holmes P V, Hellberg P, Sjöblom P
Department of Obstetrics and Gynecology, University of Gothenburg, Sweden.
Experientia. 1988 Sep 15;44(9):772-4. doi: 10.1007/BF01959160.
The present work investigates the possibility that lipoxygenase products are involved in the biochemical mechanisms of blastocyst implantation by utilizing nordihydroguaiaretic acid (NDGA) and caffeic acid (CA), inhibitors of lipoxygenase enzymes, and quinacrine (QU), an inhibitor of phospholipase-A2. It has been shown previously that inhibition of cyclooxygenase results in blockade of implantation. The inhibitors were dissolved in a standard medium and 5 microliter of the solutions were micro-injected into the uterine horns of day-4 pregnant mice. The contralateral horns acted as controls and received only vehicle. A sham-operated group provided normal controls. In 14 NDGA-treated mice, the control horns contained 40 implantations while the treated horns contained only 6 small implantations and 8 resorbing sites. These control horns were comparable to the sham controls. In 14 CA-treated mice, treated horns contained 17 small implantations plus 4 resorptions, whereas the control horns contained 26 small implantations and 4 resorptions. Twelve QU-treated mice exhibited 7 small implantations and 4 resorptions in the treated horns, plus 24 small sites and no resorptions in the control horns. Fourteen sham-operated mice had 95 implantation sites and no resorptions in their 28 horns. The results provide evidence for the involvement of the lipoxygenase enzymes and phospholipase-A2 in the initial implantation process and in the subsequent development of early pregnancy.
本研究利用去甲二氢愈创木酸(NDGA)和咖啡酸(CA)(脂氧合酶的抑制剂)以及喹吖因(QU)(磷脂酶A2的抑制剂),探讨脂氧合酶产物参与胚泡着床生化机制的可能性。先前已经表明,抑制环氧化酶会导致着床受阻。将抑制剂溶解于标准培养基中,取5微升溶液微量注射到妊娠第4天小鼠的子宫角。对侧子宫角作为对照,仅注射溶剂。假手术组作为正常对照。在14只经NDGA处理的小鼠中,对照侧子宫角有40个着床点,而处理侧子宫角仅有6个小着床点和8个吸收位点。这些对照侧子宫角与假手术对照组相当。在14只经CA处理的小鼠中,处理侧子宫角有17个小着床点加4个吸收位点,而对照侧子宫角有26个小着床点和4个吸收位点。12只经QU处理的小鼠,处理侧子宫角有7个小着床点和4个吸收位点,对照侧子宫角有24个小着床点且无吸收位点。14只假手术小鼠在其28个子宫角中有95个着床点且无吸收位点。这些结果为脂氧合酶和磷脂酶A2参与早期着床过程及随后的早期妊娠发育提供了证据。